• Patient Education

  • Ativan (Lorazepam)

    Brand names:

    Ativan®Tablet: 0.5 mg, 1 mg, 2 mg
    Injection: 2 mg/mL, 4 mg/mL
    Lorazepam Intensol®Liquid concentrate: 2 mg/mL solution
    Generic name: lorazepam (lor A ze pam)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Lorazepam And What Does It Treat?
    Lorazepam is a benzodiazepine. It is approved for the treatment of anxiety, insomnia, or sleep difficulty due to anxiety or stress, status epilepticus (continuous seizures), and as a medication given right before anesthesia. However, benzodiazepines can also be used to treat alcohol withdrawal.

    Generalized Anxiety Disorder (GAD) occurs when a person experiences excessive anxiety or worry for at least six months. Other symptoms include:

    Restlessness
    Fatigue (low energy, feeling tired all the time)
    Difficulty concentrating
    Irritability
    Muscle tension
    Sleep disturbance (difficulty falling asleep or waking up in the middle of the night)


    What Is The Most Important Information I Should Know About Lorazepam?
    Do not drive a car or operate machinery until you know how this medication affects you because you may notice that you feel tired or dizzy.

    When starting lorazepam, anxiety or insomnia may improve rapidly or over a period of days.

    Benzodiazepines, such as lorazepam, are often used for short periods of time only. They may produce emotional and/or physical dependence (addiction) even when used as recommended. With input from you, your health care provider will assess how long you will need to take the medicine.

    Do not stop taking lorazepam without talking to your healthcare provider first. Stopping lorazepam abruptly may result in one or more of the following withdrawal symptoms: irritability, nausea, tremor, dizziness, blood pressure changes, rapid heart rate, and seizures.

    The use of lorazepam with drugs like opioid medications has led to serious side effects including slowed and difficulty breathing and death. Opioid drugs are medications used to treat pain and include medications such as: codeine, oxycodone, morphine, and illegal drugs like heroin. Some opioid medications are also in cough syrup.

    If you are taking lorazepam with an opioid medication, get medical assistance immediately if you feel dizziness or sleepiness, if you have slow or troubled breathing, or if you pass out. Caregivers must get medical help right away if a patient does not respond and does not wake up.

    Avoid alcohol while taking this medication.

    Are There Specific Concerns About Lorazepam And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with anxiety disorders who wish to become pregnant face important decisions. It is important to discuss this with your doctor and caregivers.

    Regarding breastfeeding, caution is advised since lorazepam does pass into breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Lorazepam?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your healthcare provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have including obstructive sleep apnea
    All other medications you are currently taking (including over the counter products and herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are elderly or prone to falls
    If you are pregnant, plan to become pregnant, or are breastfeeding
    If you drink alcohol or use drugs
    How Should I Take Lorazepam?
    Lorazepam may be taken with or without food. Take with food if you experience an upset stomach.

    Lorazepam may be taken every day at regular times or on an as needed (“PRN”) basis. Typically, your healthcare provider will limit the number of doses you should take in one day.

    Your healthcare provider will determine the dose and method of taking the medication that is right for you based upon your response.

    Lorazepam liquid: Measure with a dosing spoon or oral syringe which you can get from your pharmacy.

    If you take the medication every day (instead of ‘as needed’), use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take it. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Lorazepam?
    If you miss a dose of lorazepam, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Lorazepam?
    Avoid drinking alcohol and using illegal drugs while you are taking lorazepam. They may decrease the benefits (e.g., worsen your condition) and increase the adverse effects (e.g., sedation) of the medication. Alcohol increases the risk of accidental overdose with medications like lorazepam.

    What Happens If I Overdose With Lorazepam?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    Symptoms of overdose include confusion, impaired coordination, slow reflexes, coma, and death.

    A specific treatment to reverse the effects of lorazepam does exist. This medicine, called flumazenil, can reverse the effects of lorazepam but must be given through an IV at a hospital. Only a doctor can decide if you need this medication.

    What Are Possible Side Effects Of Lorazepam?
    Common side effects

    Feeling dizzy, drowsy, fatigued, or lightheaded
    Impaired coordination, decreased ability to concentrate
    If you experience these side effects after starting lorazepam they will often improve over the first week or two as you continue to take the medication.

    Rare/serious side effects

    Shortness of breath, trouble speaking, feeling very tired, dizziness, or passing out.
    Increased heart rate, headache, memory impairment, irritability, restlessness
    Some people taking benzodiazepines develop a severe allergic reaction and swelling of the face. This can occur as early as with the first dose.
    Some people taking benzodiazepines for sleep have experienced various behaviors while they were asleep/not fully awake, such as sleep driving, making phone calls, and preparing or eating food. The individuals have no memory of the events when they awaken.
    Signs of feeling depressed or low mood, thoughts of harming or killing yourself, or lack of interest in life.
    Are There Any Risks For Taking Lorazepam For Long Periods Of Time?
    Lorazepam is a safe and effective medication when used as directed. Benzodiazepines may produce emotional and/or physical dependence (addiction) even when used as recommended. Physical dependence may develop after 2 or more weeks of daily use.

    What Other Medications May Interact With Lorazepam?
    Lorazepam should not be taken with other benzodiazepine medications.

    Lorazepam causes drowsiness, so caution should be used when combining it with other medications that cause drowsiness. These could include:

    Antihistamines such as diphenhydramine (Benadryl®)
    Narcotic pain medication such as morphine, oxycodone (OxyContin®), and hydrocodone (Vicodin® and Lortab®)
    Opioid cough medications such as codeine cough syrup
    Sleeping medications such as zolpidem (Ambien®)
    Other anti-anxiety medications, antipsychotic medications, certain anticonvulsant medications, and tricyclic antidepressant medications (such as amitriptyline)


    How Long Does It Take For Lorazepam To Work?
    When starting lorazepam, anxiety or insomnia may improve rapidly or over a period of days or within hours of the first dose of medication.

    Summary Of FDA Black Box Warnings
    The FDA has found that benzodiazepine drugs, such as lorazepam, when used in combination with opioid medications or other sedating medications can result in serious adverse reactions including slowed or difficult breathing and death. Patients taking opioids with benzodiazepines, other sedating medications, or alcohol, and caregivers of these patients, should seek immediate medical attention if that start to experience unusual dizziness or lightheadedness, extreme sleepiness, slow or difficulty breathing, or unresponsiveness.

  • Brand names: Trileptal®, Oxtellar XR®

    Tablet: 150 mg, 300 mg, 600 mg
    Liquid: 300 mg/5 mL
    Extended-release tablet: 150 mg, 300 mg, 600 mg
    Generic name: oxcarbazepine (ox car BAZ e peen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Oxcarbazepine And What Does It Treat?
    Oxcarbazepine is an antiepileptic medication that works in the brain to prevent and control seizures. It is approved for the treatment of partial seizures.

    Oxcarbazepine may also be helpful when prescribed “off-label” for nerve pain or as a mood stabilizer for bipolar disorder. “Off-label” means that it hasn’t been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an “off-label” treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    Bipolar disorder involves episodes of depression and/or mania.

    Symptoms of depression include:

    Depressed mood — feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, or helpless
    Loss of interest or pleasure in normal activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving in slow motion)
    Symptoms of mania include:

    Feeling irritable or “high”
    Having increased self esteem
    Feeling like you don’t need to sleep
    Feeling the need to continue to talk
    Feeling like your thoughts are too quick (racing thoughts)
    Feeling distracted
    Getting involved in activities that are risky or could have bad consequences (e.g., excessive spending)
    What Is The Most Important Information I Should Know About Oxcarbazepine?
    Bipolar disorder requires long-term treatment. Do not stop taking oxcarbazepine, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine. Missing doses of oxcarbazepine may increase your risk for a relapse in your mood symptoms.

    Do not stop taking oxcarbazepine or change your dose without talking to with your healthcare provider first.

    In order for oxcarbazepine to work properly, it should be taken every day as ordered by your healthcare provider.

    Periodically, your healthcare provider may ask you to provide a blood sample to make sure the appropriate level of medication is in your body and to assess for side effects, such as changes in blood cell counts and sodium levels.

    Are There Specific Concerns About Oxcarbazepine And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider so that he/she can best manage your medications. People living with bipolar disorder who wish to become pregnant face important decisions. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Oxcarbazepine has been associated with an increased risk of craniofacial defects and heart malformations. There may be precautions to decrease the risk of this effect. Do not stop taking oxcarbazepine without first speaking to your healthcare provider. Discontinuing mood stabilizer medications during pregnancy has been associated with a significant increase in symptom relapse.

    Regarding breast-feeding, caution is advised since oxcarbazepine does pass into breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Oxcarbazepine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you drink alcohol or use illegal drugs
    How Should I Take Oxcarbazepine?
    Oxcarbazepine is usually taken once or twice a day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 900-1200 mg per day. People taking this medication for seizure control may take up to 2400 mg daily. Only your healthcare provider can determine the correct dose for you.

    Oxcarbazepine suspension: Measure your dose with a dosing spoon or oral syringe, which you can get from your pharmacy. Before using, shake the bottle well to ensure the medicine is mixed thoroughly. Your dose can be mixed in a small glass of water just prior to taking or may be swallowed directly from the dosing spoon.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Oxcarbazepine?
    If you miss a dose of oxcarbazepine, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your dose or take more than what is prescribed.

    What Should I Avoid While Taking Oxcarbazepine?
    Avoid drinking alcohol or using illegal drugs while you are taking oxcarbazepine. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation, dizziness) of the medication.

    What Happens If I Overdose With Oxcarbazepine?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of oxcarbazepine does not exist.

    What Are Possible Side Effects Of Oxcarbazepine?
    Common side effects

    Dizziness
    Drowsiness
    Vision changes
    Nausea/vomiting
    Headache
    Fatigue
    Uncoordinated movements
    Tremor
    Rare/serious side effects

    Oxcarbazepine can cause a decrease in the body’s sodium level. Some signs of low sodium include nausea, tiredness, lack of energy, headache, confusion, or more frequent or more severe seizures.

    Oxcarbazepine may also cause allergic reactions or serious problems which may affect organs and other parts of your body like the liver or blood cells. You may or may not have a rash with these types of reactions.

    In rare cases (

    Studies have found that individuals who take antiepileptic medications including oxcarbazepine may be twice as likely to have suicidal thoughts or behaviors as individuals who take placebo (inactive medication). These thoughts or behaviors are rare and occurred in approximately 1 in 500 patients taking the antiepileptic class of medications. If you experience any thoughts or impulses to hurt yourself, you should contact your doctor immediately.

    Are There Any Risks For Taking Oxcarbazepine For Long Periods Of Time?
    To date, there are no known problems associated with long term use of oxcarbazepine. It is a safe and effective medication when used as directed.

    It is important to note that some of the side effects listed above (particularly changes in blood sodium, rash, and suicidal thoughts) may continue to occur or worsen if you continue taking the medication. It is important to follow up with your doctor for blood work and to contact your doctor immediately if you notice any skin rash or changes in mood or behavior.

    What Other Medications May Interact With Oxcarbazepine?
    The seizure medications phenobarbital and phenytoin may decrease the effects of oxcarbazepine.

    Oxcarbazepine may increase the effects of phenobarbital and phenytoin.

    Oxcarbazepine may decrease the level and effects of:

    Oral contraceptives (birth control pills)
    Anti-rejection medications used in organ transplants, like tacrolimus (Prograf®) and cyclosporine (Neoral®, Sandimmune®)
    Certain blood pressure medications, such as amlodipine (Norvasc®) or felodipine (Plendil®)
    How Long Does It Take For Oxcarbazepine To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking oxcarbazepine and whether or not you are experiencing any side effects from the medication. It will probably take several weeks to see big enough changes in your symptoms to decide if oxcarbazepine is the right medication for you.

    Mood stabilizer treatment is generally needed lifelong for persons with bipolar disorder. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Summary Of FDA Black Box Warnings
    There are no FDA black box warnings for oxcarbazepine.

  • Propranolol

    Pronounced: pro PRAN oh lol
    Brand Names: Hemangeol, Inderal LA, Inderal XL, InnoPran XL
    What is the most important information I should know about propranolol?
     

    You should not use this medicine if you have asthma, very slow heart beats, or a serious heart condition such as "sick sinus syndrome" or "AV block" (unless you have a pacemaker).

    Babies who weigh less than 4.5 pounds should not be given Hemangeol oral liquid.

     

    What is propranolol?
    Propranolol is a beta-blocker. Beta-blockers affect the heart and circulation (blood flow through arteries and veins).

    Propranolol is used to treat tremors, angina (chest pain), hypertension (high blood pressure), heart rhythm disorders, and other heart or circulatory conditions. It is also used to treat or prevent heart attack, and to reduce the severity and frequency of migraine headaches.

    Hemangeol (propranolol oral liquid 4.28 milligrams) is given to infants who are at least 5 weeks old to treat a genetic condition called infantile hemangiomas. Hemangiomas are caused by blood vessels grouping together in an abnormal way. These blood vessels form benign (non-cancerous) growths that can develop into ulcers or red marks on the skin. Hemangiomas can also cause more serious complications inside the body (in the liver, brain, or digestive system).

    Propranolol may also be used for purposes not listed in this medication guide.

    What should I discuss with my healthcare provider before taking propranolol?
     

    You should not use propranolol if you are allergic to it, or if you have:

    asthma;
    very slow heart beats that have caused you to faint; or
    a serious heart condition such as "sick sinus syndrome" or "AV block" (unless you have a pacemaker).
    Babies who weigh less than 4.5 pounds should not be given Hemangeol oral liquid.

    To make sure propranolol is safe for you, tell your doctor if you have:

    a muscle disorder;
    bronchitis, emphysema, or other breathing disorders;
    low blood sugar, or diabetes (propranolol can make it harder for you to tell when you have low blood sugar);
    slow heartbeats, low blood pressure;
    congestive heart failure;
    depression;
    liver or kidney disease;
    a thyroid disorder;
    pheochromocytoma (tumor of the adrenal gland); or
    problems with circulation (such as Raynaud's syndrome).
    It is not known whether propranolol will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medicine.

    Propranolol can pass into breast milk and may harm a nursing baby. Tell your doctor if you are breast-feeding a baby.

     

    How should I take propranolol?
     

    Follow all directions on your prescription label. Your doctor may occasionally change your dose to make sure you get the best results. Do not take this medicine in larger or smaller amounts or for longer than recommended.

    Adults may take propranolol with or without food, but take it the same way each time.

    Take this medicine at the same time each day.

    Do not crush, chew, break, or open an extended-release capsule. Swallow it whole.

    Hemangeol must be given to an infant during or just after a feeding. Doses should be spaced at least 9 hours apart. Make sure your child gets fed regularly while taking this medicine. Tell your doctor when the child has any changes in weight. Hemangeol doses are based on weight in children, and any changes may affect your child's dose.

    Call your doctor if a child taking Hemangeol is sick with vomiting, or has any loss of appetite.

    Measure liquid medicine with the dosing syringe provided, or with a special dose-measuring spoon or medicine cup. If you do not have a dose-measuring device, ask your pharmacist for one.

    Do not shake Hemangeol liquid.

    Your blood pressure will need to be checked often.

    If you need surgery, tell the surgeon ahead of time that you are using propranolol. You may need to stop using the medicine for a short time.

    Do not skip doses or stop using propranolol suddenly. Stopping suddenly may make your condition worse. Follow your doctor's instructions about tapering your dose.

    This medicine can cause unusual results with certain medical tests. Tell any doctor who treats you that you are using propranolol.

    If you are being treated for high blood pressure, keep using this medicine even if you feel well. High blood pressure often has no symptoms. You may need to use blood pressure medicine for the rest of your life.

    Propranolol is only part of a complete program of treatment for hypertension that may also include diet, exercise, and weight control. Follow your diet, medication, and exercise routines very closely if you are being treated for hypertension.

    Store at room temperature away from moisture and heat. Do not allow liquid medicine to freeze. Throw away any unused Hemangeol 2 months after you first opened the bottle.

     What happens if I miss a dose?

    For regular (short-acting) propranolol: Take the missed dose as soon as you remember. Skip the missed dose if your next dose is less than 4 hours away.

    For extended-release propranolol (Inderal LA, InnoPran XL and others): Take the missed dose as soon as you remember. Skip the missed dose if your next dose is less than 8 hours away.

    Do not take extra medicine to make up the missed dose.

    What happens if I overdose?
     Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

    Overdose symptoms may include slow or uneven heartbeats, dizziness, weakness, or fainting.

     

    What should I avoid while taking propranolol?
    Avoid drinking alcohol. It may increase your blood levels of propranolol.

    Avoid getting up too fast from a sitting or lying position, or you may feel dizzy. Get up slowly and steady yourself to prevent a fall.

    What are the possible side effects of propranolol?
     

    Get emergency medical help if you have signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat.

    Call your doctor at once if you have:

    slow or uneven heartbeats;
    a light-headed feeling, like you might pass out;
    wheezing or trouble breathing;
    shortness of breath (even with mild exertion), swelling, rapid weight gain;
    sudden weakness, vision problems, or loss of coordination (especially in a child with hemangioma that affects the face or head);
    cold feeling in your hands and feet;
    depression, confusion, hallucinations;
    liver problems--nausea, upper stomach pain, itching, tired feeling, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes);
    low blood sugar--headache, hunger, weakness, sweating, confusion, irritability, dizziness, fast heart rate, or feeling jittery;
    low blood sugar in a baby--pale skin, blue or purple skin, sweating, fussiness, crying, not wanting to eat, feeling cold, drowsiness, weak or shallow breathing (breathing may stop for short periods), seizure (convulsions), or loss of consciousness; or
    severe skin reaction--fever, sore throat, swelling in your face or tongue, burning in your eyes, skin pain, followed by a red or purple skin rash that spreads (especially in the face or upper body) and causes blistering and peeling.
    Common side effects may include:

    nausea, vomiting, diarrhea, constipation, stomach cramps;
    decreased sex drive, impotence, or difficulty having an orgasm;
    sleep problems (insomnia); or
    tired feeling.
    This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

     

    What other drugs will affect propranolol?
    Tell your doctor about all medicines you use, and those you start or stop using during your treatment with propranolol, especially:

    a blood thinner--warfarin, Coumadin, Jantoven;
    an antidepressant--amitriptyline, clomipramine, desipramine, imipramine, and others;
    drugs to treat high blood pressure or a prostate disorder--doxazosin, prazosin, terazosin;
    heart or blood pressure medicine--amiodarone, diltiazem, propafenone, quinidine, verapamil, and others;
    NSAIDs (nonsteroidal anti-inflammatory drugs)--aspirin, ibuprofen (Advil, Motrin), naproxen (Aleve), celecoxib, diclofenac, indomethacin, meloxicam, and others; or
    steroid medicine--prednisone and others.
    This list is not complete. Other drugs may interact with propranolol, including prescription and over-the-counter medicines, vitamins, and herbal products. Not all possible interactions are listed in this medication guide.

    Where can I get more information?
    Your pharmacist can provide more information about propranolol.

  • Xanax (Alprazolam)
     

    Xanax®Tablets: 0.25 mg, 0.5 mg, 1 mg, 2 mg
    Xanax XR®Extended release tablets: 0.5 mg, 1 mg, 2 mg, 3 mg
    Niravam®Orally disintegrating tablets: 0.25 mg, 0.5 mg, 1 mg, 2 mg
    Alprazolam Intensol®Liquid (concentrate): 1 mg/ml
    Generic name: alprazolam (al PRAY zoe lam)

    All FDA black box barnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Alprazolam And What Does It Treat?
    Alprazolam is a benzodiazepine. It is approved for the treatment of generalized anxiety disorder (GAD) and panic disorder with or without agoraphobia. However, benzodiazepines are also commonly used to treat difficulty sleeping and alcohol withdrawal.

    Generalized Anxiety Disorder (GAD) occurs when a person experiences excessive anxiety or worry for at least six months. Other symptoms include:

    Restlessness
    Fatigue (low energy, feeling tired all the time)
    Difficulty concentrating
    Irritability
    Muscle tension
    Sleep disturbance (difficulty falling asleep or waking up in the middle of the night)
    Panic Disorder occurs when a person experiences unexpected and repeated episodes of intense fear. These episodes have physical symptoms including chest pain, shortness of breath, heart palpitations, sweating, dizziness, and nausea. Fear of future episodes is also part of panic disorder.

    What Is The Most Important Information I Should Know About Alprazolam?
    Do not drive a car or operate machinery until you know how this medication affects you because you may notice that you feel tired or dizzy.

    When starting alprazolam, anxiety or insomnia may improve rapidly or over a period of days.

    Benzodiazepines, such as alprazolam, are often used for short periods of time only. They may produce emotional and/or physical dependence (addiction) even when used as recommended. With input from you, your health care provider will assess how long you will need to take the medicine.

    Do not stop taking alprazolam without talking to your healthcare provider first. Stopping alprazolam abruptly may result in one or more of the following withdrawal symptoms: irritability, nausea, tremor, dizziness, blood pressure changes, rapid heart rate, and seizures.

    The use of alprazolam with drugs like opioid medications has led to serious side effects including slowed and difficulty breathing and death. Opioid drugs are medications used to treat pain and include medications such as: codeine, oxycodone, morphine, and illegal drugs like heroin. Some opioid medications are also in cough syrup.

    If you are taking alprazolam with an opioid medication, get medical assistance immediately if you feel dizziness or sleepiness, if you have slow or troubled breathing, or if you pass out. Caregivers must get medical help right away if a patient does not respond and does not wake up.

    Avoid alcohol while taking this medication.

    Are There Specific Concerns About Alprazolam And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with anxiety disorders who wish to become pregnant face important decisions. It is important to discuss this with your doctor and caregivers.

    Regarding breastfeeding, caution is advised since alprazolam does pass into breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Alprazolam?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your healthcare provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have including obstructive sleep apnea
    All other medications you are currently taking (including over the counter products and herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication
    If you are elderly or are prone to falls
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you drink alcohol or use drugs
    How Should I Take Alprazolam?
    Alprazolam may be taken with or without food. Take with food if you experience an upset stomach.

    Alprazolam may be taken every day at regular times or on an as needed (“PRN”) basis. Typically, your healthcare provider will limit the number of doses you should take in one day.

    Your healthcare provider will determine the dose and method of taking the medication that is right for you based upon your response.

    Alprazolam orally disintegrating tablets must remain in their original packaging. Open the package with clean dry hands before each dose. Do not try to put tablets in a pillbox if you take the orally disintegrating tablets. Take the tablets right away, do not store for later use.

    Alprazolam orally disintegrating tablets will dissolve in your mouth within seconds and can be swallowed with or without liquid.

    Extended release tablets: Swallow whole. Do not chew, crush or split tablet.

    Alprazolam liquid: Measure with a dosing spoon or oral syringe, which you can get from your pharmacy.

    If you take the medication every day (instead of ‘as needed’), use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take it. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Alprazolam?
    If you miss a dose of alprazolam, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Alprazolam?
    Avoid drinking alcohol and using illegal drugs while you are taking alprazolam. They may decrease the benefits (e.g., worsen your condition) and increase the adverse effects (e.g., sedation) of the medication. Alcohol increases the risk of accidental overdose with medications like alprazolam.

    What Happens If I Overdose With Alprazolam?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    Symptoms of overdose include confusion, impaired coordination, slow reflexes, coma, and death.

    A specific treatment to reverse the effects of alprazolam does exist. This medicine, called flumazenil, can reverse the effects of alprazolam but must be given through an IV at a hospital. Only a doctor can decide if you need this medication.

    What Are Possible Side Effects Of Alprazolam?
    Common side effects

    Feeling dizzy, drowsy, fatigued, or lightheaded
    Impaired coordination, decreased ability to concentrate
    If you experience these side effects after starting clonazepam they will often improve over the first week or two as you continue to take the medication

    Rare/serious side effects

    Shortness of breath, trouble speaking, feeling very tired, dizziness, or passing out.
    Increased heart rate, headache, memory impairment, irritability, and restlessness may occur.
    Some people taking benzodiazepines develop a severe allergic reaction and swelling of the face. This can occur as early as with the first dose.
    Some people taking benzodiazepines for sleep have experienced various behaviors while they were asleep/not fully awake, such as sleep driving, making phone calls, and preparing or eating food. The individuals have no memory of the events when they awaken.
    Signs of feeling depressed or low mood, thoughts of harming or killing yourself, or lack of interest in life.
    Are There Any Risks For Taking Alprazolam For Long Periods Of Time?
    Alprazolam is a safe and effective medication when used as directed. Benzodiazepines may produce emotional and/or physical dependence (addiction) even when used as recommended. Physical dependence may develop after 2 or more weeks of daily use.

    What Other Medications May Interact With Alprazolam?
    The following medications may increase the levels and effects of alprazolam:

    Ketoconazole (Nizoral®), itraconazole (Sporanox®), nefazodone (Serzone®), fluvoxamine (Luvox®), and cimetidine (Tagamet®)
    The following medications may decrease the levels and effects of alprazolam:

    Carbamazepine (Tegretol®), phenytoin (Dilantin®), and phenobarbital (Luminal®)
    Alprazolam should not be taken with other benzodiazepine medications.

    Alprazolam may cause drowsiness, so caution should be used when combining it with other medications that cause drowsiness. These could include:

    Antihistamines such as diphenhydramine (Benadryl®)
    Narcotic pain medication such as morphine, oxycodone (OxyContin®), and hydrocodone (Vicodin® and Lortab®)
    Opioid cough medications such as codeine cough syrup
    Sleeping medications such as zolpidem (Ambien®)
    Other anti-anxiety medications, antipsychotic medications, certain anticonvulsant medications, and tricyclic antidepressant medications (such as amitriptyline)
    How Long Does It Take For Alprazolam To Work?
    When starting alprazolam, anxiety or insomnia may improve rapidly or over a period of days or within hours of the first dose of medication.

    Summary Of FDA Black Box Warnings
    The FDA has found that benzodiazepine drugs, such as alprazolam, when used in combination with opioid medications or other sedating medications can result in serious adverse reactions including slowed or difficult breathing and death. Patients taking opioids with benzodiazepines, other sedating medications, or alcohol, and caregivers of these patients, should seek immediate medical attention if that start to experience unusual dizziness or lightheadedness, extreme sleepiness, slow or difficulty breathing, or unresponsiveness.

  • Adderall (Amphetamine)
     
    Brand names:

    Adderall® (mixed amphetamine salts) – immediate releaseTablet: 5 mg, 7.5 mg, 10 mg, 12.5 mg, 15 mg, 20 mg, 30 mg
    Adderall XR® (mixed amphetamine salts) – extended releaseCapsules: 5 mg, 10 mg, 15 mg, 20 mg, 25 mg, 30 mg
    Dexedrine® (dextroamphetamine) – immediate releaseTablet: 5 mg
    Elixir: 1 mg/mL
    Dexedrine Spansules® (dextroamphetamine) – sustained releaseCapsules: 5 mg, 10 mg, 15 mg
    Vyvanse® (lisdexamfetamine dimesylate)Capsules: 10 mg, 20 mg, 30 mg, 40 mg, 50 mg, 60 mg, 70 mg
    Tablet (chewable): 10 mg, 20 mg, 30 mg, 40 mg, 50 mg, 60 mg
    Generic name: amphetamine (am FET a meen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Are Amphetamine, Mixed Amphetamine Salts, Dextroamphetamine, Lisdexamfetamine And What Do They Treat?
    Mixed amphetamine salts, dextroamphetamine, and lisdexamfetamine are prescription medications that are used to treat individuals with attention-deficit hyperactivity disorder (ADHD). Lisdexamfetamine is also used to treat moderate to severe binge eating disorder. These medications are also known as stimulants.

    Symptoms of ADHD interfere with an individual’s ability to function at school or work or in social settings and include:

    Inattention (e.g., making careless mistakes, losing things necessary for tasks)
    Hyperactivity (e.g., inability to sit still)
    Impulsivity (e.g., interrupting or intruding on others)
    Hyperactivity is less common in adults.  A person may have severe inattention without hyperactivity or impulsivity.

    Stimulants are used in addition to non-medication treatments to manage ADHD symptoms.

    What Is The Most Important Information I Should Know About Mixed Amphetamine Salts, Dextroamphetamine, Lisdexamfetamine?
    Although some symptoms may improve within days of starting stimulants, it may take several weeks before you notice the full benefits of the medication.

    Are There Specific Concerns About Mixed Amphetamine Salts, Dextroamphetamine, Lisdexamfetamine And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with ADHD who wish to become pregnant face important decisions. There is very little information available regarding the risks of stimulants in pregnancy when taken as prescribed for ADHD. Abuse of stimulants (i.e., taking without a prescription or taking more than prescribed) has been associated with premature delivery, low birth weight, and neonatal withdrawal symptoms. Untreated ADHD may be associated with increased risk of substance use. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Stimulants are not recommended with breastfeeding according to the American Academy of Pediatrics. Stimulants may concentrate in breast milk and have negative effects on the infant.

    What Should I Discuss With My Healthcare Provider Before Taking Mixed Amphetamine Salts, Dextroamphetamine, Lisdexamfetamine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    If you experience side effects from your medications, discuss them with your provider. Some side effects pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, including heart disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you drink alcohol or use drugs
    How Should I Take Mixed Amphetamine Salts, Dextroamphetamine, Lisdexamfetamine?
    Stimulants are usually taken 1 to 2 times per day with or without food.

    Tablets (Dexedrine®, Adderall®): Swallow the tablets whole. Chewing the tablets gives an unpleasant taste and can irritate the mouth and throat.
    Sprinkle capsules (Adderall XR®, Dexedrine Spansule®): Swallow whole or sprinkle onto food, such as applesauce or pudding and eat immediately. Do not chew sprinkle capsules or contents.
    Long-acting capsules (Vyvanse®): Swallow whole or open capsule and mix contents with water. Use all of the powder from the capsule. Drink entire glass of water right away after mixing.
    Liquid (Dexedrine®): Measure with a dosing spoon or oral syringe which you can get from your pharmacy
    The dose of stimulant medication is variable. Only your healthcare provider can determine the correct dose for you.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Mixed Amphetamine Salts, Dextroamphetamine, Lisdexamfetamine?
    If you miss a dose of stimulant, take it as soon as you remember if it is still early in the day. Do not take a missed dose after 5:00 PM, as this may interfere with sleep. Do not take a missed dose of extended-release capsules after 2:00 PM, as this may interfere with sleep. Discuss missed doses with your healthcare provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Takingmixed Amphetamine Salts, Dextroamphetamine, Lisdexamfetamine?
    Avoid drinking alcohol or using illegal drugs while you are taking this medication. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Mixed Amphetamine Salts, Dextroamphetamine, Lisdexamfetamine?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of stimulants does not exist.

    What Are Possible Side Effects Of Mixed Amphetamine Salts, Dextroamphetamine, Lisdexamfetamine?
    Common side effects

    Upset stomach, loss of appetite, insomnia, and mild anxiety
    Rare side Effects

    Contact your healthcare provider if any of the following occur while taking stimulants:

    Significant increases in blood pressure or heart rate, shortness of breath, fatigue
    Severe anxiety, panic attacks, mania, hallucinations, paranoia or delusions
    Severe muscle pain, weakness, signs of dehydration, or dark urine
    Prolonged or painful erection
    Changes of feeling or color in your fingers or toes
    Serious side effects

    Misuse of amphetamine medications may cause sudden death and serious cardiovascular adverse events. Amphetamine medications should be avoided in individuals who have a heart defect (structural abnormality), uncontrolled high blood pressure, or other disorder of heart.

    Are There Any Risks For Taking Mixed Amphetamine Salts, Dextroamphetamine, Lisdexamfetamine?
    Stimulants are Schedule II controlled substances. There is a risk of physical and/or emotional dependence (addiction) when they are taken for long periods of time.

    Although treatment with stimulant medications can slow growth, many studies have shown that these changes are small. Children may catch up with growth over time; therefore, it should not be a concern for most children. Height, weight, and eating habits should be discussed before treatment starts and regularly during treatment. If you are concerned about your child’s growth, discuss other possible treatments with your child’s doctor.

    What Other Medications May Interact With Mixed Amphetamine Salts, Dextroamphetamine, Lisdexamfetamine?
    Medications used to treat depression can interact with amphetamine medications resulting in serious reactions including high body temperature, high blood pressure, and seizures (convulsions). Tell your healthcare provider if you are beginning or have recently discontinued any of these medications.

    Stimulants should not be taken with or within 2 weeks of monoamine oxidase inhibitor antidepressants (MAOIs), including phenelzine (Nardil®), Tranylcypromine (Parnate®), selegiline (Emsam®), and isocarboxazid (Marplan®) or the antibiotic linezolid (Zyvox®).  Taking stimulants with or within 2 weeks of MAOIs can result in seizures, fever or dangerously high blood pressure that can lead to death.

    The following medications may increase the levels and/or effects of stimulant medications:

    Increase levels: Antacids (e.g., sodium bicarbonate, calcium carbonate [Tums®]), acetazolamide
    Increase side effects: Atomoxetine (Strattera®), caffeine, phenylephrine, fluoxetine (Prozac®), bupropion (Wellbutrin®), venlafaxine (Effexor®), duloxetine (Cymbalta®), Modafinil (Provigil®), and armodafinil (Nuvigil®)
    The following foods/medications may decrease the levels and effects of stimulant medications: ascorbic acid (vitamin C), acidic beverages (e.g., orange juice, grapefruit juice)

    Stimulant medications may decrease the effects of blood pressure medications.

    How Long Does It Take For Mixed Amphetamine Salts, Dextroamphetamine, Lisdexamfetamine To Work?
    Although you may experience beneficial effects from stimulants within a few days of starting the medication, it often takes several weeks to get the full effect of the medication. Your healthcare provider may also need to gradually adjust the dose to find the dose that works best for you.

    Summary Of FDA Black Box Warnings
    Sudden Cardiac Death

    Misuse of amphetamines may cause sudden death or serious cardiovascular adverse events.

    Dependence

    Amphetamines have a high potential for abuse.  Prolonged use of amphetamines may lead to drug dependence.  Particular attention should be paid to the possibility of subjects obtaining amphetamines for non-therapeutic use or distribution to others.  They should be prescribed or dispensed sparingly.

  • Strattera (Atomoxetine)

    Capsules: 10 mg, 18 mg, 25 mg, 40 mg, 60 mg, 80 mg, 100 mg
    Generic Name: atomoxetine (AT oh mox e teen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Atomoxetine And What Does It Treat?
    Atomoxetine is a prescription medication that is used to treat individuals with attention deficit hyperactivity disorder (ADHD).

    Symptoms of ADHD interfere with an individual’s ability to function at school or work or in social settings and include:

    Inattention (e.g., making careless mistakes, losing things necessary for tasks)
    Hyperactivity (e.g., inability to sit still)
    Impulsivity (e.g., interrupting or intruding on others)
    Hyperactivity is less common in adults. A person may have severe inattention without hyperactivity or impulsivity.

    Atomoxetine is used in addition to non-medication treatments to manage ADHD symptoms.

    What Is The Most Important Information I Should Know About Atomoxetine?
    It may take several weeks before you notice the full benefits of this medication. It is important to continue taking atomoxetine as directed, even if you do not notice immediate improvement.

    Are There Specific Concerns About Atomoxetine And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with ADHD who wish to become pregnant face important decisions. Untreated ADHD has risks for the fetus as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Regarding breastfeeding, caution is advised since it is not known if atomoxetine passes into human breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Atomoxetine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    If you experience side effects from your medications, discuss them with your provider. Some side effects pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, including heart disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you drink alcohol or use drugs
    How Should I Take Atomoxetine?
    Atomoxetine is usually taken one to two times per day with or without food.

    The dose usually ranges from 20 mg to 100 mg. Only your health care provider can determine the correct dose for you.

    Capsules should be swallowed whole, not crushed or chewed.

    Use a calendar, pillbox, alarm clock or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Atomoxetine?
    If you miss a dose of atomoxetine, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your health care provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Atomoxetine?
    Avoid drinking alcohol or using illegal drugs while you are taking this medication. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Atomoxetine?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of atomoxetine does not exist.

    What Are Possible Side Effects Of Atomoxetine?
    Common side effects

    Upset stomach, nausea, vomiting, decreased appetite, constipation, dry mouth, headache
    Feeling sleepy, sluggish or weak during the day, trouble sleeping at night
    Decreased libido or sexual side effects
    Rare side effects

    Menstrual cycle changes, urinary retention, hot flushes, sweating, severe fatigue, irritability, or mood swings
    Rarely, a painful prolonged erection has been reported in child, adolescent, and adult males
    Increased heart rate and blood pressure
    Risk of switching to hypomania and mania, particularly in individuals with bipolar disorder
    Serious side effects

    Liver toxicity, increased suicidal thoughts, angioedema and cardiovascular complications
    Are There Any Risks For Taking Atomoxetine For Long Periods Of Time?
    There are no known problems associated with long term use of atomoxetine

    What Other Medications May Interact With Atomoxetine?
    Atomoxetine should not be taken with or within two weeks of monoamine oxidase inhibitor antidepressants (MAOIs), including phenelzine (Nardil®), Tranylcypromine (Parnate®), selegiline (Emsam®), isocarboxazid (Marplan®), or antibiotic linezolid (Zyvox®). Taking atomoxetine with or within 2 weeks of MAOIs can result in seizures, fever or dangerously high blood pressure that can lead to death.

    The following medications may increase the levels and effects of atomoxetine:

    Paroxetine (Paxil®), Fluoxetine (Prozac®), and Quinidine (Quinidex®)
    Medications for asthma/difficulty breathing (e.g., albuterol) can increase the risk of high blood pressure and rapid heart rate (tachycardia) when taking atomoxetine.

    Because of atomoxetine’s possible effect on blood pressure it should be used cautiously with other medications that increase or decrease blood pressure.

    How Long Does It Take For Atomoxetine To Work?
    It may take four to eight weeks to get the maximum benefit once the right dose is determined. However, improvements in some symptoms may occur sooner.

    Summary Of FDA Black Box Warnings
    Suicidal thoughts or actions

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide.
    In short-term studies, atomoxetine increased the risk of suicidality in children, adolescents and young adults when compared to placebo.
    Patients should be closely monitored for suicidality (suicidal thinking and behavior), worsening of symptoms or changes in behavior.
    Families and caregivers should be advised of the need for close observation and communication with the prescriber.

  • Wellbutrin (Bupropion)

    Wellbutrin SR®Tablets: 100 mg, 150 mg, 200 mg
    Wellbutrin XL®Tablets: 150 mg, 300 mg
    Zyban®Tablets: 150 mg
    Forfivo XL®Tablets: 450 mg
    Aplenzin®Tablets: 174 mg, 348 mg, 522 mg
    Bupropion hydrochlorideImmediate release tablets: 75mg, 100 mg
    Sustained release tablets: 100 mg, 150 mg, 200 mg
    Extended release tablets: 150 mg, 300 mg
    Bupropion hydrobromide Extended release tablets: 174 mg, 348 mg, 522 mg

    Generic name: bupropion (byoo PRO pee on)
    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Bupropion And What Does It Treat?
    Bupropion is an antidepressant medication that works in the brain. It is approved for the treatment of major depressive disorder (MDD), seasonal affective disorder (SAD), and to help people quit smoking (smoking cessation).

    Symptoms of depression include:

    Depressed mood - feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, and helpless
    Loss of interest or pleasure in your usual activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving and thinking in slow motion)
    Suicidal thoughts or behaviors

    SAD is a type of depression that occurs mainly during the autumn-winter season. Although the common term SAD is now referred to as Major Depression with Seasonal Pattern, this fact sheet will continue to use SAD as it is more commonly known.

    Bupropion may also be helpful when prescribed “off-label” for bipolar disorder, attention deficit hyperactivity disorder (ADHD, and sexual dysfunction due to SSRI antidepressants. “Off-label” means that it hasn’t been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an “off-label” treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Bupropion?
    After starting bupropion, symptoms gradually decrease over a period of weeks. In MDD and SAD, sleep and other physical symptoms may improve before there is noticeable improvement in mood or interest in activities. Once symptoms are under control, MDD usually requires long-term treatment to help prevent the return of depressive symptoms. If you are using bupropion for SAD or smoking cessation, the length of your treatment may be shorter. With input from you, your health care provider will assess how long you will need to take the medicine.

    Do not stop taking bupropion or change your dose without talking with your health care provider first.

    Depression is also a part of bipolar illness. People with bipolar disorder who take antidepressants may be at risk for "switching" from depression into mania. Symptoms of mania include "high" or irritable mood, very high self-esteem, decreased need for sleep, pressure to keep talking, racing thoughts, being easily distracted, frequently involved in activities with a large risk for bad consequences (for example, excessive buying sprees).

    Are There Specific Concerns About Bupropion And Pregnancy?
    If you are planning on becoming pregnant, notify your health care provider to best manage your medications. People living with MDD who wish to become pregnant face important decisions, each with risks and benefits as they relate to how the illness, medications, and risks to the fetus may interact. Untreated MDD has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers. 

    Bupropion has also been evaluated for smoking cessation during pregnancy and is recommended only after other therapies have failed.

    Caution is advised with breastfeeding since bupropion does pass into breast milk.

    What Should I Discuss With My Health Care Provider Before Taking Bupropion?
    Symptoms of your condition that bother you most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require an adjustment in the medication. 
    Any other psychiatric or medical problems you have, including a history of bipolar disorder
    All other medications you are currently taking and any medication allergies you have. This will help your prescriber assess for potential drug interactions. 
    Other non-medication treatment you are receiving (such as psychotherapy (i.e., talk therapy) or substance abuse treatment). Your provider can explain how these different treatments work with the medication. 
    If you are pregnant, plan to become pregnant, or are breastfeeding
    If you drink alcohol or use drugs

    How Should I Take Bupropion?
    Bupropion hydrochloride is available in 3 different forms: immediate release (IR), sustained release (SR), and extended release (XL).

    Bupropion IR is usually taken 2 or 3 times per day with 4-6 hours between doses. The dose usually ranges from 100 mg twice daily to 150 mg three times daily, with the last dose taken mid-afternoon.

    Bupropion SR is usually taken twice daily in the morning and mid-afternoon. The dose usually ranges from 100 mg twice daily up to 200 mg twice daily.

    Bupropion XL is usually taken once daily in the morning. The dose ranges from 150 mg to 450 mg.

    Bupropion hydrobromide (Aplenzin®) is usually taken once daily in the morning. The dose ranges from 174 mg to 522 mg.

    While there are dose ranges for each form, your health care provider will determine the form and dose that is right for you based on your response.

    The dose for SAD is bupropion XL 150 mg once daily in the morning. The dose may be increased to 300 mg once daily.

    The dose for smoking cessation is bupropion SR 150 mg once daily for 3 days and then twice daily for 7 to 12 weeks.

    You should not take more than one product that contains bupropion, including the products that are used to quit smoking. Do not take more than your prescribed dose since higher doses may increase your risk of having a seizure. Since quickly increasing the dose of bupropion can cause seizures in some people, your doctor will slowly increase your dose.

    You can take bupropion on an empty stomach or with food. The SR and XL forms should be swallowed whole — not chewed, crushed, or broken — so that the medication can work correctly in your body and to reduce the risk of serious side effects. The tablet shell from the SR and XL forms may appear in your feces.

    Consider using a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Bupropion?
    For bupropion IR or SR, if you miss a dose, take it as soon as you remember. Take the remaining doses for the day at evenly spaced times at least 4 hours apart. DO NOT take 2 doses at once. You should not take more than your prescribed dose and doing so may increase your risk of having a seizure.

    For bupropion XL, do not take an extra tablet to make up for the dose you forgot. Wait and take your next dose at your regular time the next day.

    What Should I Avoid While Taking Bupropion?
    Avoid drinking alcohol or using illegal drugs while you are taking bupropion because the beneficial effects of the medication may be decreased and the risk of seizures may be increased. If you are dependent on drugs or alcohol and would like to stop, consult your healthcare provider for help. Abruptly stopping these substances can result in a seizure, especially when taking bupropion.

    What Happens If I Overdose With Bupropion?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    What Are The Possible Side Effects Of Bupropion?
    Common side effects

    Headache, weight loss, dry mouth, trouble sleeping (insomnia), nausea, dizziness, constipation, fast heartbeat, and sore throat. These will often improve over the first week or two as you continue to take the medication.

    Rare/serious side effects

    Less than 10% of patients will experience skin rash, sweating, ringing in the ears, shakiness, stomach pain, muscle pain, thought disturbances, anxiety or angle closure glaucoma (symptoms of angle closure glaucoma may include eye pain, changes in vision, swelling or redness in or around eye).

    Unlike many antidepressants, bupropion does not commonly cause sexual side effects and may be selected as an alternative treatment when antidepressant-induced sexual side effects are problematic. Sexual side effects include such problems as difficulty achieving orgasm or ejaculatory delay.

    In general the risk of seizures due to bupropion is low. The risk of having a seizure increases with higher than recommended doses of bupropion, a history of seizures or head injury, tumor in the brain, severe liver disease, an eating disorder, alcohol or drug dependence, or taking other drugs that can also increase your risk of having a seizure.

    There is a low risk of cardiovascular adverse events associated with stimulating agents, including bupropion. This risk increases if you have heart disease, high blood pressure, previous heart attack, or irregular heartbeat, or when used with transdermal nicotine replacement products. In these cases, a thorough cardiovascular evaluation is recommended before starting this medicine.

    Are There Any Risks For Taking Bupropion For Long Periods Of Time?
    To date, there are no known problems associated with long term use of bupropion. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Bupropion?
    Bupropion should not be taken with or within two weeks of taking monoamine oxidase inhibitors (MAOIs). These include phenelzine (Nardil®), tranycypromine (Parnate®), isocarboxazid (Marplan®), and selegiline (Emsam®).

    There are several products with the active ingredient bupropion. Do not take more than one product that contains bupropion since this may increase your risk of having a seizure.

    Certain medications may increase your risk of having a seizure when combined with bupropion. These include other antidepressants, antipsychotics, theophylline, isoniazid, tramadol, stimulants, steroids, hypoglycemic agents (including insulin), certain antibiotics (e.g., Cipro®), and abrupt discontinuation of benzodiazepines (e.g., Ativan®).

    Notify your doctor and pharmacist if you are taking any of the following medications: phenytoin (Dilantin®), carbamazepine (Tegretol®, Equetro®), phenobarbital, cimetidine (Tagamet®), ritonavir (Norvir®), lopinavir (Kaletra™), nelfinavir (Viracept®), or efavirenz (Sustiva®). These medications can change the way your body reacts to bupropion.

    Notify your doctor and pharmacist if you are taking any of the following medications: atomoxetine (Stratterra®), codeine, tamoxifen, tetrabenazine, thioridazine (Mellaril®), tramadol (Ultram®), or a tricyclic antidepressant. Bupropion can change the way your body reacts to these medications.

    How Long Does It Take For Bupropion To Work?
    Sleep, energy, or appetite may show some improvement within the first 1-2 weeks. Improvement in these physical symptoms can be an important early signal that the medication is working. Depressed mood and lack of interest in actiities may need up to 6-8 weeks to fully improve. 

    Summary Of FDA Black Box Warnings
    Suicidal thoughts or actions in children and adults

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide. Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking antidepressant medications. This risk may persist until significant remission occurs.

    In short-term studies, antidepressants increased the risk of suicidality in children, adolescents and young adults when compared to placebo. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24. Adults ages 65 and older taking antidepressants have a decreased risk of suicidality. Patients, their families and caregivers should be alert to the emergence of anxiety, restlessness, irritability, aggressiveness and insomnia. If these symptoms emerge, they should be reported to the patient’s prescriber or healthcare professional. All patients being treated with antidepressants for any indication should watch for and notify their healthcare provider for worsening symptoms, suicidality and unusual changes in behavior, especially during the first few months of treatment.

  • BuSpar (Buspirone)

    Tablet: 5 mg, 7.5 mg, 10 mg, 15 mg, 30 mg
    Generic name: buspirone (byoo SPYE rone)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Buspirone And What Does It Treat?
    Buspirone is in a class of medications called anti-anxiety medications. Buspirone is not related to other anti-anxiety medications, such as benzodiazepines, barbiturates or other sedative/ anxiolytic drugs. It is approved for the treatment of generalized anxiety disorder (GAD).

    Generalized Anxiety Disorder (GAD) occurs when a person experiences excessive anxiety or worry for at least six months. Other symptoms include:

    Restlessness
    Fatigue (low energy, feeling tired all the time)
    Difficulty concentrating
    Irritability
    Muscle tension
    Sleep disturbance (difficulty falling asleep or waking up in the middle of the night)
    What Is The Most Important Information I Should Know About Buspirone?
    Do not drive a car or operate machinery until you know how this medication affects you because you may notice that you feel tired or dizzy.

    Alcohol may increase any drowsiness or dizziness when taken with buspirone. You should avoid the use of alcohol while taking buspirone.

    It may take 3 to 4 weeks before you start to feel better. Initially you may begin to notice a decrease in irritability and worry. Do not stop taking this medication without talking to your healthcare provider first. With input from you, your health care provider will assess how long you will need to take the medicine.

    Unlike other anti-anxiety medications, buspirone has very low abuse potential.

    Are There Specific Concerns About Buspirone And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with anxiety disorders who wish to become pregnant face important decisions. It is important to discuss this with your doctor and caregivers.

    Regarding breastfeeding, caution is advised since it is unknown whether buspirone passes into breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Buspirone?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your healthcare provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have
    All other medications you are currently taking (including over the counter products and herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you drink alcohol or use drugs
    How Should I Take Buspirone?
    Buspirone should be taken twice a day with or without food.

    Your healthcare provider will determine the dose that is right for you based upon your response.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Buspirone?
    If you miss a dose of buspirone, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Buspirone?
    Avoid drinking alcohol and using illegal drugs while you are taking buspirone. They may decrease the benefits (e.g., worsen your condition) and increase the adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Buspirone?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of buspirone does not exist.

    What Are Possible Side Effects Of Buspirone?
    Common side effects

    Nausea, headache, or changes in dreams
    Feeling dizzy, drowsy, or lightheaded
    Rare/serious side effects

    Changes in weight or appetite, fainting, changes in blood pressure, muscle cramps or spasms, and redness or itching of eyes may occur in some instances.

    Allergic reaction (difficulty breathing; hives; swelling of your lips, tongue or face); chest pain or an irregular heartbeat; slurred speech; confusion or blurred vision; numbness or tingling in your hands, feet, arms, or legs; or uncontrollable movements of your arms, legs, tongue, or lips.

    Are There Any Risks For Taking Buspirone For Long Periods Of Time?
    To date, there are no known problems associated with the long term use of buspirone. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Buspirone?
    If you have taken a monoamine oxidase inhibitor (MAOI), such as phenelzine (Nardil®), isocarboxazid (Marplan®), selegiline (Eldepryl®, EMSAM®) or tranylcypromine (Parnate®), within the past 2 weeks, do not take buspirone. The use of buspirone with these agents can cause a severe increase in your blood pressure.

    The following medications may increase the levels and effects of buspirone:

    Diltiazem (Cardizem®, Dilacor®, Tiazac®)
    Verapamil (Calan®, Covera-HS®, Isoptin®, Verelan®)
    Erythromycin (E-Mycin®, E.E.S.®, Ery-Tab®, Eryc®, others)
    Consuming large amounts of grapefruit juice can increase the amount of buspirone in your blood

    The following medications may decrease the levels and effects of buspirone:

    Rifampin (Rifadin®, Rimactane®, Rifampicin®, others)
    How Long Does It Take For Buspirone To Work?
    It may take 3 to 4 weeks of taking buspirone every day before you start to feel better.

    Summary Of FDA Black Box Warnings
    There are no FDA black box warnings for buspirone.

  • Tegretol (Carbamazepine)

    Tegretol®Tablet: 200 mg, 400 mg
    Chewable tablet: 100 mg
    Oral suspension: 100 mg/5 mL
    Tegretol XR®Extended release tablet: 100 mg, 200 mg, 400 mg
    Carbatrol®, Equetro®Extended release capsule: 100 mg, 200 mg, 300 mg
    Epitol®Tablet: 200 mg
    Generic name: carbamazepine (kar ba MAZ e peen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Carbamazepine And What Does It Treat?
    Carbamazepine is a mood stabilizer medication that works in the brain. It is approved for the treatment of bipolar 1 disorder (also known as manic depression) as well as for epilepsy and trigeminal neuralgia. Bipolar disorder involves episodes of depression and/or mania.

    Symptoms of depression include:

    Depressed mood — feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, or helpless
    Loss of interest or pleasure in normal activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving in slow motion)
    Symptoms of mania include:

    Feeling irritable or “high”
    Having increased self esteem
    Feeling like you don’t need to sleep
    Feeling the need to continue to talk
    Feeling like your thoughts are too quick (racing thoughts)
    Feeling distracted
    Getting involved in activities that are risky or could have bad consequences (e.g., excessive spending)
    Carbamazepine may also be helpful when prescribed “off-label” for behavioral or psychological symptoms of dementia. “Off-label” means that it hasn’t been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an “off-label” treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Carbamazepine?
    Bipolar disorder requires long-term treatment. Do not stop taking carbamazepine, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine. Missing doses of carbamazepine may increase your risk for a relapse in your mood symptoms.

    Do not stop taking carbamazepine or change your dose without talking to with your healthcare provider first.

    In order for carbamazepine to work properly, it should be taken every day as ordered by your healthcare provider.

    Periodically, your healthcare provider may ask you to provide a blood sample to make sure the appropriate level of medication is in your body and to assess for side effects, such as changes in blood cell counts.

    Are There Specific Concerns About Carbamazepine And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider so that he/she can best manage your medications. People living with bipolar disorder who wish to become pregnant face important decisions. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Carbamazepine has been associated with and increased risk of defects of the head and face, fingernails, and developmental delay. There may be precautions to decrease the risk of this effect. Do not stop taking carbamazepine without first speaking to your healthcare provider. Discontinuing mood stabilizer medications during pregnancy has been associated with a significant increase in symptom relapse.

    Regarding breast-feeding, caution is advised since carbamazepine does pass into breast milk. Talk with your doctor about whether or not it is safe to breastfeed while taking carbamazepine.

    What Should I Discuss With My Healthcare Provider Before Taking Carbamazepine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you drink alcohol or use illegal drugs
    How Should I Take Carbamazepine?
    Carbamazepine is usually taken 2-4 times per day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 200 mg to 1600 mg each day, but some patients may require more based on symptoms. Only your healthcare provider can determine the correct dose for you.

    Carbamazepine suspension: Measure with a dosing spoon or oral syringe, which you can get from your pharmacy.

    Extended-release capsules: Swallow whole or sprinkle onto food, such as applesauce or pudding and eat immediately. Do not chew the sprinkle capsule or contents.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Carbamazepine?
    If you miss a dose of carbamazepine, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your dose or take more than what is prescribed.

    What Should I Avoid While Taking Carbamazepine?
    Avoid drinking alcohol or using illegal drugs while you are taking carbamazepine. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    Avoid consuming large quantities (8 ounces or more) of fresh grapefruit juice, as this can increase levels of carbamazepine and increase your risk of side effects or rash.

    What Happens If I Overdose With Carbamazepine?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of carbamazepine does not exist.

    What Are Possible Side Effects Of Carbamazepine?
    Common side effects

    Dizziness or drowsiness
    Unsteadiness when standing or walking
    Nausea or vomiting
    Dry mouth
    Constipation
    Blurry or double vision

    Rare/serious side effects

    Carbamazepine can cause a decrease in the body’s sodium level. Some signs of low sodium include nausea, tiredness, lack of energy, headache, confusion, or more frequent or more severe seizures.

    Carbamazepine may cause rare but serious blood problems including low white blood cell counts. Symptoms may include: fever, sore throat, or other infections that come and go or do not go away, easy bruising, red or purple spots on your body, bleeding gums or nose bleeds, or severe fatigue or weakness. Your doctor will occasionally order blood work to monitor for this.

    In rare cases (

    Studies have found that individuals who take antiepileptic medications including carbamazepine have suicidal thoughts or behaviors up to twice as often than individuals who take placebo (inactive medication). These thoughts or behaviors occurred in approximately 1 in 500 patients taking the antiepileptic class of medications. If you experience any thoughts or impulses to hurt yourself, you should contact your doctor immediately.

    Are There Any Risks For Taking Carbamazepine For Long Periods Of Time?
    To date, there are no known problems associated with long term use of carbamazepine. It is a safe and effective medication when used as directed.

    It is important to note that some of the side effects listed above (particularly changes in blood sodium, rash, and suicidal thoughts) may continue to occur or worsen if you continue taking the medication. It is important to follow up with your doctor for blood work and to contact your doctor immediately if you notice any skin rash or changes in mood or behavior.

    What Other Medications May Interact With Carbamazepine?
    The following medications may increase the level and effects of carbamazepine:

    The mood stabilizer and antiseizure medication valproic acid/divalproex (Depakote®)
    Certain antibiotics, such as ciprofloxacin (Cipro®), erythromycin (Ery-tab®), clarithrymycin (Biaxin®)
    Medications for heartburn or reflux, such as cimetidine (Tagamet®) and omeprazole (Prilosec®)
    Antifungal medications, such as ketoconazole (Nizoral®), fluconazole (Diflucan®), itraconazole (Sporanox®), voriconazole (Vfend®)
    Certain heart medications, such as diltiazem (Cardizem®) or verapamil (Calan®, Isoptin®)
    Certain medications used for mood or sleep, such as trazodone (Desyrel®) or nefazodone (Serzone®)
    The following medications may decrease the level and effect of carbamazepine:>/p>

    Phenytoin (Dilantin®), phenobarbital, primidone (Mysoline®)
    Rifampin (Rifadin®)
    Carbamazepine may decrease the level and effects of:

    Oral contraceptives (birth control pills)
    Certain medications used for psychiatric disorders, such as lurasidone (Latuda®), aripiprazole (Abilify®), alprazolam (Xanax®), escitalopram (Lexapro®), trazodone (Desyrel®), and nefazodone (Serzone®)
    Certain heart medications, such as diltiazem (Cardizem®) or verapamil (Calan®, Isoptin®)
    Anti-rejection medications used in organ transplants, like tacrolimus (Prograf®) and cyclosporine (Neoral®, Sandimmune®)
    Certain cholesterol medications, like simvastatin (Zocor®), atorvastatin (Lipitor®)
    The blood thinner warfarin (Coumadin®)
    Antiseizure medications like phenytoin (Dilantin®), phenobarbital, and valproic acid/divalproex (Depakote®), lamotrigine (Lamictal®)
    How Long Does It Take For Carbamazepine To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking carbamazepine. It will probably take several weeks to see big enough changes in your symptoms to decide if carbamazepine is the right medication for you.

    Mood stabilizer treatment is generally needed lifelong for persons with bipolar disorder. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Summary Of FDA Black Box Warnings
    Serious skin reactions and HLA-B*1502 allele

    Serious and sometimes fatal skin reactions have been reported with carbamazepine use. These reactions may be accompanied by mucous membrane ulcers, fever, or painful rash. Seek medical care immediately at the first sign of rash, as treatment must be stopped to avoid progression of the rash. These reactions are estimated to occur in 1 to 6 per 10,000 new users in countries with mainly Caucasian populations, but the risk in some Asian countries is estimated to be about 10 times higher. HLA-B*1502 is found almost exclusively in patients with ancestry across broad areas of Asia. Patients with ancestry in genetically at-risk populations should be screened for the presence of HLA-B*1502 prior to initiating treatment with carbamazepine.

    Aplastic anemia and agranulocytosis

    Carbamazepine has been associated with a condition where the body does not make enough new blood cells and also with a decrease in white blood cells. People taking carbamazepine can be at an increased risk of infection if white blood cell counts drop too low.

  • Vraylar (Cariprazine)

    Capsules: 1.5mg, 3mg, 4.5mg, 6mg capsules
    Generic name: cariprazine (kar IP ra zeen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Cariprazine And What Does It Treat?
    Cariprazine is a medication that works in the brain to treat schizophrenia. It is also known as a second-generation antipsychotic (SGA) or atypical antipsychotic. Cariprazine rebalances dopamine and serotonin to improve thinking, mood, and behavior.

    Symptoms of schizophrenia include:

    Hallucinations — imagined voices or images that seem real
    Delusions — beliefs that are not true (e.g., other people are reading your thoughts)
    Disorganized thinking or trouble organizing your thoughts and making sense
    Little desire to be around other people
    Trouble speaking clearly
    Lack of motivation
    Cariprazine may help some or all of these symptoms.

    Cariprazine is also FDA approved for the following indications:

    Acute treatment of manic or mixed episodes of bipolar I disorder
    This medication sheet will focus primarily on schizophrenia. More information on bipolar disorder can be found here.

    Cariprazine may also be helpful when prescribed "off-label" for other mental health conditions. "Off-label" means that it has not been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an "off-label" treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Cariprazine?
    Schizophrenia requires long-term treatment. Do not stop taking cariprazine even when you feel better.

    With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of cariprazine may increase your risk for a relapse in your symptoms.

    Do not stop taking cariprazine or change your dose without talking to with your healthcare provider first.

    For cariprazine to work properly, it should be taken every day as ordered by your healthcare provider.

    Are There Specific Concerns About Cariprazine And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with schizophrenia who wish to become pregnant face important decisions. This is a complex decision since untreated schizophrenia has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Antipsychotic use during the third trimester of pregnancy has a risk for abnormal muscle movements (extrapyramidal symptoms [EPS]) and/or withdrawal symptoms in newborns following delivery. Symptoms in the newborn may include agitation, feeding disorder, hypertonia, hypotonia, respiratory distress, somnolence, and tremor; these effects may be self-limiting or require hospitalization.

    Caution is advised with breast-feeding. It is unknown whether cariprazine is present in breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Cariprazine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you ever had muscle stiffness, shaking, tardive dyskinesia, neuroleptic malignant syndrome, or weight gain caused by a medication
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any psychiatric or medical problems you have, such as heart rhythm problems, long QT syndrome, heart attacks, diabetes, high cholesterol or seizures
    If you have a family history of diabetes or heart disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these treatments work with the medication.
    If you are pregnant, plan to become pregnant or are breast-feeding
    If you smoke, drink alcohol or use illegal drugs
    How Should I Take Cariprazine?
    Cariprazine is usually taken once daily with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 1.5mg to 6mg. Only your healthcare provider can determine the correct dose for you.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication.You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Cariprazine?
    If you miss a dose of cariprazine, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Cariprazine?
    Avoid drinking alcohol or using illegal drugs while you are taking cariprazine. They may decrease the benefits (e.g., worsen your confusion) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Cariprazine?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of cariprazine does not exist.

    What Are Possible Side Effects Of Cariprazine?
    Common side effects

    Extrapyramidal symptoms, restlessness, headache, insomnia, nausea

    Rare/serious side effects

    Cariprazine may increase the blood levels of a hormone called prolactin. Side effects of increased prolactin levels include females losing their period, production of breast milk and males losing their sex drive or possbly experiencing erectile problems. Long term (months or years) of elevated prolactin can lead to osteoporosis, or increased risk of bone fractures.

    Some people may develop muscle related side effects while taking cariprazine. The technical terms for these are “extrapyramidal symptoms” (EPS) and “tardive dyskinesia” (TD). Symptoms of EPS include restlessness, tremor, and stiffness. TD symptoms include slow or jerky movements that one cannot control, often starting in the mouth with tongue rolling or chewing movements.

    Temperature regulation: Impaired core body temperature regulation may occur; caution with strenuous exercise, heat exposure, and dehydration.

    Second generation antipsychotics (SGAs) increase the risk of weight gain, high blood sugar, and high cholesterol. This is also known as metabolic syndrome. Your healthcare provider may ask you for a blood sample to check your cholesterol, blood sugar, and hemoglobin A1c (a measure of blood sugar over time) while you take this medication.

    Information on healthy eating and adding exercise to decrease your chances of developing metabolic syndrome may be found at the following sites:http://www.helpguide.org/articles/healthy-eating/healthy-eating.htm
    http://www.helpguide.org/home-pages/exercise-fitness.htm
    SGAs have been linked with higher risk of death, strokes, and transient ischemic attacks (TIAs) in elderly people with behavior problems due to dementia.

    All antipsychotics have been associated with the risk of sudden cardiac death due to an arrhythmia (irregular heartbeat). To minimize this risk, antipsychotic medications should be used in the smallest effective dose when the benefits outweigh the risks. Your doctor may order an EKG to monitor for irregular heartbeat.

    Neuroleptic malignant syndrome is a rare, life threatening adverse effect of antipsychotics which occurs in

    All antipsychotics can cause sedation, dizziness, or orthostatic hypotension (a drop in blood pressure when standing up from sitting or lying down). These side effects may lead to falls which could cause bone fractures or other injuries. This risk is higher for people with conditions or other medications that could worsen these effects. If falls or any of these symptoms occur, contact your healthcare provider.

    Are There Any Risks For Taking Cariprazine For Long Periods Of Time?
    Tardive dyskinesia (TD) is a side effect that develops with prolonged use of antipsychotics.

    Medications such as cariprazine have been shown to have a lower risk of TD compared to older antipsychotics, such as Haldol® (haloperidol). If you develop symptoms of TD, such as grimacing, sucking, and smacking of lips, or other movements that you cannot control, contact your healthcare provider immediately. All patients taking either first or second-generation antipsychotics should have an Abnormal Involuntary Movement Scale (AIMS) completed regularly by their healthcare provider to monitor for TD.

    Second generation antipsychotics (SGAs) increase the risk of diabetes, weight gain, high cholesterol, and high triglycerides. (See “Serious Side Effects” section for monitoring recommendations).

    What Other Medications May Interact With Cariprazine?
    The following medications may increase the levels and effects of cariprazine: itraconazole, ketoconazole

    The following medications may decrease the levels and effects of cariprazine: rifampin, carbamazepine

    How Long Does It Take For Cariprazine To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking cariprazine. It will probably take several weeks to see big enough changes in your symptoms to decide if cariprazine is the right medication for you.

    Antipsychotic treatment is generally needed lifelong for persons with schizophrenia. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Hallucinations, disorganized thinking, and delusions may improve in the first 1-2 weeks
    Sometimes these symptoms do not completely go away
    Motivation and desire to be around other people can take at least 1-2 weeks to improve
    Symptoms continue to get better the longer you take cariprazine.
    It may take 2-3 months before you get the full benefit of cariprazine.
    Summary Of FDA Black Box Warnings
    Increased mortality in elderly patients with dementia-related psychosis

    Both first generation (typical) and second generation (atypical) antipsychotics are associated with an increased risk of mortality in elderly patients when used for dementia related psychosis.
    Although there were multiple causes of death in studies, most deaths appeared to be due to cardiovascular causes (e.g. sudden cardiac death) or infection (e.g. pneumonia).
    Antipsychotics are not indicated for the treatment of dementia-related psychosis.

  • Celexa (Citalopram)

    Brand names:

    Celexa®Tablets: 10 mg, 20 mg, 40 mg
    CitalopramTablets: 10 mg, 20 mg, 40 mg
    Liquid: 10 mg/5 ml

    Generic name: citalopram (sye TAL oh pram)

    All FDA black box warnings are at the end of this fact sheet.  Please review before taking this medication.

    What Is Citalopram And What Does It Treat?
    Citalopram is an antidepressant medication that works in the brain. It is approved for the treatment of major depressive disorder (MDD).

    Symptoms of depression include:

    Depressed mood - feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, and helpless
    Loss of interest or pleasure in your usual activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving and thinking in slow motion)
    Suicidal thoughts or behaviors

    Citalopram may also be helpful when prescribed “off-label” for obsessive-compulsive disorder, generalized anxiety disorder, panic disorder, social phobia (also known as social anxiety disorder), posttraumatic stress disorder, eating disorders such as binge eating disorder, and premenstrual dysphoric disorder (PMDD). “Off-label” means that it hasn’t been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an “off-label” treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Citalopram?
    Do not stop taking citalopram even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of citalopram may increase your risk for relapse in your symptoms.

    Stopping citalopram abruptly may result in one or more of the following withdrawal symptoms: irritability, nausea, feeling dizzy, vomiting, nightmares, headache, and/or paresthesias (prickling, tingling sensation on the skin).

    Depression is also a part of bipolar illness. People with bipolar disorder who take antidepressants may be at risk for "switching" from depression into mania. Symptoms of mania include "high" or irritable mood, very high self-esteem, decreased need for sleep, pressure to keep talking, racing thoughts, being easily distracted, frequently involved in activities with a large risk for bad consequences (for example, excessive buying sprees).

    Medical attention should be sought if serotonin syndrome is suspected. Please refer to serious side effects for signs/symptoms.

    Are There Specific Concerns About Citalopram And Pregnancy?
    If you are planning on becoming pregnant, notify your health care provider to best manage your medications. People living with MDD who wish to become pregnant face important decisions. Untreated MDD has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers. For women who take antidepressant medications during weeks 13 through the end of their pregnancy (second and third trimesters), there is a risk that the baby can be born before it is fully developed (before 37 weeks).

    For mothers who have taken SSRIs during their pregnancy, there appears to be less than a 1% chance of infants developing persistent pulmonary hypertension. This is a potentially fatal condition that is associated with use of the antidepressant in the second half of pregnancy. However, women who discontinued antidepressant therapy were five times more likely to have a depression relapse than those who continued their antidepressant. If you are pregnant, please discuss the risks and benefits of antidepressant use with your health care provider.

    Caution is advised with breastfeeding since citalopram does pass into breast milk.

    What Should I Discuss With My Health Care Provider Before Taking Citalopram?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, including a history of bipolar disorder
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breastfeeding
    If you drink alcohol or use drugs

    How Should I Take Citalopram?
    Citalopram is usually taken one time per day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 20 mg to 40 mg once daily. For patients older than 60 years, the maximum recommended dose is 20 mg once daily. Only your health care provider can determine the correct dose for you.

    The liquid should be measured with a dosing spoon or oral syringe which you can get from your pharmacy.

    If you are taking citalopram, you should not take other medications that include escitalopram (Lexapro®).

    Consider using a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Citalopram?
    If you miss a dose of citalopram, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your health care provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Citalopram?
    Avoid drinking alcohol or using illegal drugs while you are taking antidepressant medications. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Citalopram?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of citalopram does not exist.

    What Are The Possible Side Effects Of Citalopram?
    Common side effects

    Headache, nausea, diarrhea, dry mouth, increased sweating, feeling nervous, restless, fatigue, or having trouble sleeping (insomnia). These will often improve over the first week or two as you continue to take the medication.

    Sexual side effects, such as problems with orgasm or ejaculatory delay often do not diminish over time.

    Rare/serious side effects

    Low sodium blood levels (symptoms of low sodium levels may include headache, weakness, difficulty concentrating and remembering), teeth grinding, angle closure glaucoma (symptoms of angle closure glaucoma may include eye pain, changes in vision, swelling or redness in or around eye), serotonin syndrome (symptoms may include shivering, diarrhea, confusion, severe muscle tightness, fever, seizures, and death), seizure

    SSRI antidepressants including citalopram may increase the risk of bleeding events. Combined use of aspirin, nonsteroidal anti-inflammatory drugs (e.g., ibuprofen, naproxen), warfarin, and other anti-coagulants may increase this risk. This may include symptoms such as gums that bleed more easily, nose bleed, or gastrointestinal bleeding. Some cases have been life threatening.

    Risk of abnormal heart rhythms with citalopram

    August 2011: Citalopram at doses greater than 40 mg per day could potentially cause a dangerous abnormality in the electrical activity of the heart. Citalopram use is discouraged in patients with congenital long QT syndrome. Patients with low levels of potassium and magnesium in the blood are also at increased risk. If you are currently taking citalopram at a dose greater than 40 mg per days, talk to your health care professional. Seek immediate care if you experience an irregular heartbeat, shortness of breath, dizziness, or fainting while taking citalopram. If you are taking citalopram, your health care professional may occasionally order an electrocardiogram (ECG, EKG) to monitor your heart rate and rhythm. Your health care provider may also order tests to check levels of potassium and magnesium in your blood.

    Are There Any Risks For Taking Citalopram For Long Periods Of Time?
    To date, there are no known problems associated with long term use of citalopram. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Citalopram?
    Citalopram should not be taken with or within 2 weeks of taking monoamine oxidase inhibitors (MAOIs). These include phenelzine (Nardil®), tranylcypromine (Parnate®), isocarboxazid (Marplan®), rasagiline (Azilect®), and selegiline (Emsam®).

    Although rare, there is an increased risk of serotonin syndrome when citalopram is used with other medications that increase serotonin, such as other antidepressants, migraine medications called “triptans” (e.g., Imitrex®), some pain medications (e.g., tramadol (Ultram®), the antibiotic linezolid (Zyvox®), and amphetamines.

    Citalopram may increase the effects of other medications that can cause bleeding (e.g., ibuprofen (Advil®, Motrin®), warfarin (Coumadin®) and aspirin).

    Increased risk of QT prolongation when used with:

    Certain antiarrhythmics: quinidine (Quinidex Extentabs®, Quinaglute®, Quinalan®), procainamide (Procanbid®, Pronestyl®, Pronestyl-SR®), amiodarone (Cordarone®, Pacerone®), sotalol (Betapace®, Sorine®)
    Certain antipsychotics: chlorpromazine (Thorazine®), thioridazine (Mellaril®)
    Certain antibiotics: gatifloxacin (Tequin®), moxifloxacin (Avelox®)
    Methadone®

    How Long Does It Take For Citalopram To Work?
    Sleep, energy, or appetite may show some improvement within the first 1-2 weeks. Improvement in these physical symptoms can be an important early signal that the medication is working. Depressed mood and lack of interest in activities may need up to 6-8 weeks to fully improve.

    Summary Of FDA Black Box Warnings
    Suicidal thoughts or actions in children and adults

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide. Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking antidepressant medications. This risk may persist until significant remission occurs.

    In short-term studies, antidepressants increased the risk of suicidality in children, adolescents, and young adults when compared to placebo. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24. Adults age 65 and older taking antidepressants have a decreased risk of suicidality. Patients, their families, and caregivers should be alert to the emergence of anxiety, restlessness, irritability, aggressiveness and insomnia. If these symptoms emerge, they should be reported to the patient’s prescriber or health care professional. All patients being treated with antidepressants for any indication should watch for and notify their health care provider for worsening symptoms, suicidality and unusual changes in behavior, especially during the first few months of treatment.

  •  Klonopin (Clonazepam)

    Brand name: Klonopin®

    Tablet: 0.5 mg, 1 mg, 2 mg
    Wafer (orally disintegrating tablet): 0.125 mg, 0.25 mg, 0.5 mg, 1 mg, 2 mg
    Generic name: clonazepam (kloe NA ze pam)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Clonazepam And What Does It Treat?
    Clonazepam is a benzodiazepine. It is approved for the treatment of panic disorder (with or without agoraphobia), as well as certain types of seizure disorders. However, benzodiazepines are also commonly used to treat difficulty sleeping and alcohol withdrawal.

    Panic Disorder occurs when a person experiences unexpected and repeated episodes of intense fear. These episodes have physical symptoms including chest pain, shortness of breath, heart palpitations, sweating, dizziness, and nausea. Fear of future episodes is also part of panic disorder.

    What Is The Most Important Information I Should Know About Clonazepam?
    Do not drive a car or operate machinery until you know how this medication affects you because you may notice that you feel tired or dizzy.

    When starting clonazepam, anxiety or insomnia may improve rapidly or over a period of days.

    Benzodiazepines, such as clonazepam, are often used for short periods of time only. They may produce emotional and/or physical dependence (addiction) even when used as recommended. With input from you, your health care provider will assess how long you will need to take the medicine.

    Do not stop taking clonazepam without talking to your healthcare provider first. Stopping clonazepam abruptly may result in one or more of the following withdrawal symptoms: irritability, nausea, tremor, dizziness, blood pressure changes, rapid heart rate, and seizures.

    The use of clonazepam with drugs like opioid medications has led to serious side effects including slowed and difficulty breathing and death. Opioid drugs are medications used to treat pain and include medications such as: codeine, oxycodone, morphine, and illegal drugs like heroin. Some opioid medications are also in cough syrup.

    If you are taking clonazepam with an opioid medication, get medical assistance immediately if you feel dizziness or sleepiness, if you have slow or troubled breathing, or if you pass out. Caregivers must get medical help right away if a patient does not respond and does not wake up.

    Avoid alcohol while taking this medication.

    Are There Specific Concerns About Clonazepam And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with anxiety disorders who wish to become pregnant face important decisions. It is important to discuss this with your doctor and caregivers.

    Regarding breastfeeding, caution is advised since clonazepam does pass into breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Clonazepam?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your healthcare provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have including obstructive sleep apnea
    All other medications you are currently taking (including over the counter products and herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication
    If you are elderly or are prone to falls
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you drink alcohol or use drugs
    How Should I Take Clonazepam?
    Clonazepam may be taken with or without food. Take with food if you experience an upset stomach.

    Clonazepam may be taken every day at regular times or on an as needed (“PRN”) basis. Typically, your healthcare provider will limit the number of doses you should take in one day.

    Your healthcare provider will determine the dose and method of taking the medication that is right for you based upon your response.

    Clonazepam oral disintegrating tablets must remain in their original packaging. Open the package with clean dry hands before each dose. Do not try to put tablets in a pillbox if you take the orally disintegrating tablets. Take the tablets right away, do not store for later use.

    Clonazepam oral disintegrating tablets will dissolve in your mouth within seconds and can be swallowed with or without liquid.

    If you take the medication every day (instead of ‘as needed’), use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take it. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Clonazepam?
    If you miss a dose of clonazepam, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Clonazepam?
    Avoid drinking alcohol and using illegal drugs while you are taking clonazepam. They may decrease the benefits (e.g., worsen your condition) and increase the adverse effects (e.g., sedation) of the medication. Alcohol increases the risk of accidental overdose with medications like clonazepam.

    What Happens If I Overdose With Clonazepam?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    Symptoms of overdose include confusion, impaired coordination, slow reflexes, coma, and death.

    A specific treatment to reverse the effects of clonazepam does exist. This medicine, called flumazenil, can reverse the effects of clonazepam but must be given through an IV at a hospital. Only a doctor can decide if you need this medication.

    What Are Possible Side Effects Of Clonazepam?
    Common side effects

    Feeling dizzy, drowsy, fatigued, or lightheaded
    Impaired coordination, decreased ability to concentrate
    If you experience these side effects after starting clonazepam they will often improve over the first week or two as you continue to take the medication.

    Rare/serious side effects

    Shortness of breath, trouble speaking, feeling very tired, dizziness, or passing out.
    Increased heart rate, headache, memory impairment, irritability, and restlessness may occur.
    Some people taking benzodiazepines develop a severe allergic reaction and swelling of the face. This can occur as early as with the first dose.
    Some people taking benzodiazepines for sleep have experienced various behaviors while they were asleep/not fully awake, such as sleep driving, making phone calls, and preparing or eating food. The individuals have no memory of the events when they awaken.
    Signs of feeling depressed or low mood, thoughts of harming or killing yourself, or lack of interest in life.
    Are There Any Risks For Taking Clonazepam For Long Periods Of Time?
    Clonazepam is a safe and effective medication when used as directed. Benzodiazepines may produce emotional and/or physical dependence (addiction) even when used as recommended. Physical dependence may develop after 2 or more weeks of daily use.

    What Other Medications May Interact With Clonazepam?
    The following medications may increase the levels and effects of clonazepam:

    Ketoconazole (Nizoral®), itraconazole (Sporanox®), nefazodone (Serzone®), fluvoxamine (Luvox®), and cimetidine (Tagamet®)
    The following medications may decrease the levels and effects of clonazepam:

    Carbamazepine (Tegretol®), phenytoin (Dilantin®), and phenobarbital (Luminal®)
    Clonazepam should not be taken with other benzodiazepine medications.

    Clonazepam may cause drowsiness, so caution should be used when combining it with other medications that cause drowsiness. These could include:

    Antihistamines such as diphenhydramine (Benadryl®)
    Narcotic pain medication such as morphine, oxycodone (OxyContin®), and hydrocodone (Vicodin® and Lortab®)
    Opioid cough medications such as codeine cough syrup
    Sleeping medications such as zolpidem (Ambien®)
    Other anti-anxiety medications, antipsychotic medications, certain anticonvulsant medications, and tricyclic antidepressant medications (such as amitriptyline)
    How Long Does It Take For Clonazepam To Work?
    When starting clonazepam, anxiety or insomnia may improve rapidly or over a period of days or within hours of the first dose of medication.

    Summary Of FDA Black Box Warnings
    The FDA has found that benzodiazepine drugs, such as clonazepam, when used in combination with opioid medications or other sedating medications can result in serious adverse reactions including slowed or difficult breathing and death. Patients taking opioids with benzodiazepines, other sedating medications, or alcohol, and caregivers of these patients, should seek immediate medical attention if that start to experience unusual dizziness or lightheadedness, extreme sleepiness, slow or difficulty breathing, or unresponsiveness.

  • Kapvay and Catapres (Clonidine)

    Brand names:

    Kapvay®Tablet (extended release): 0.1 mg
    Catapres®Tablet (immediate release): 0.1 mg, 0.2 mg, 0.3 mg
    Generic name: Clonidine (KLON i deen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Clonidine And What Does It Treat?
    Clonidine is a prescription medication that is used to treat attention-deficit hyperactivity disorder (ADHD) in individuals between 6 and 17 years of age. Clonidine is also used to treat high blood pressure in both children and adults.

    Symptoms of ADHD interfere with an individual’s ability to function at school or work or in social settings and include:

    Inattention (e.g., making careless mistakes, losing things necessary for tasks)
    Hyperactivity (e.g., inability to sit still)
    Impulsivity (e.g., interrupting or intruding on others)
    A person may have severe inattention without hyperactivity or impulsivity.

    Clonidine is used in addition to non-medication treatments to manage ADHD symptoms.

    What Is The Most Important Information I Should Know About Clonidine?
    Although some symptoms may improve within days of starting clonidine, it may take several weeks before you notice the full benefits of the medication.

    Are There Specific Concerns About Clonidine And Pregnancy?
    If you are planning on becoming pregnant, notify your health care provider so that he/she can best manage your medications. People living with ADHD who wish to become pregnant face important decisions. There are no well-controlled studies of clonidine use in pregnant women. Animal studies did not demonstrate evidence of fetal harm. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Regarding breastfeeding, caution is advised since clonidine does pass into breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Clonidine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    If you experience side effects from your medications, discuss them with your provider. Some side effects pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, including heart disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you drink alcohol or use drugs
    How Should I Take Clonidine?
    Clonidine is usually taken one to two times per day with or without food.

    The dose usually ranges from 0.1 mg to 0.4 mg per day. Only your healthcare provider can determine the correct dose for you.

    Extended release tablets (Kapvay®) should not be crushed, chewed or divided. Swallow the tablet whole.

    What Happens If I Miss A Dose Of Clonidine?
    If you miss a dose of clonidine take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your health care provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Clonidine?
    Clonidine may cause dizziness or drowsiness, especially when first starting the medication. Make sure you know how you react to the medication before you drive, operate machinery, or participate in other activities that may be dangerous if you are not alert.

    Avoid drinking alcohol or using illegal drugs while you are taking this medication. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Clonidine?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    Overdosing with clonidine may cause sleepiness, dizziness, low blood pressure and slow heart rate.

    A specific treatment to reverse the effects of clonidine does not exist.

    What Are Possible Side Effects Of Clonidine?
    Common side effects

    Sleepiness, drowsiness, dizziness, headache, irritability
    ​Low blood pressure
    Nausea, stomach pain, dry mouth, constipation and decreased appetite
    Rare/serious side effects

    Very low blood pressure or heart rate
    ​Fainting
    Are There Any Risks For Taking Clonidine For Long Periods Of Time?
    There are no known problems associated with long term use of clonidine.

    What Other Medications May Interact With Clonidine?
    The following medications may increase the effects of clonidine:

    Medications that lower blood pressure or cause sedation (sleepiness)
    Other products containing clonidine or guanfacine (Tenex® or Intuniv®)
    How Long Does It Take For Clonidine To Work?
    It may take four to eight weeks to get the maximum benefit once the right dose is determined. However, improvements in some symptoms may occur sooner. Your health care provider may also need to adjust gradually the dose to find the dose that works best for you.

  • Pristiq (Desvenlafaxine)

    Brand names:

    Pristiq®Tablets (extended release): 25 mg, 50 mg, 100 mg
    Khedezla®Tablets (extended release): 50 mg, 100 mg
    DesvenlafaxineTablets (extended release): 25 mg, 50 mg, 100 mg

    Generic name: Desvenlafaxine (des ven la FAX een)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Desvenlafaxine And What Does It Treat?
    Desvenlafaxine is an antidepressant medication that works in the brain. It is approved for the treatment of major depressive disorder (MDD).

    Symptoms of depression include:

    Depressed mood - feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, and helpless
    Loss of interest or pleasure in your usual activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving and thinking in slow motion)
    Suicidal thoughts or behaviors

    What Is The Most Important Information I Should Know About Desvenlafaxine?
    Do not stop taking desvenlafaxine, even when you feel better.  With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of desvenlafaxine may increase your risk for relapse in your symptoms.

    Stopping desvenlafaxine abruptly may result in one or more of the following withdrawal symptoms: irritability, nausea, feeling dizzy, vomiting, nightmares, headache, and/or paresthesias (prickling, tingling sensation on the skin).

    Depression is also a part of bipolar illness. People with bipolar disorder who take antidepressants may be at risk for "switching" from depression into mania. Symptoms of mania include "high" or irritable mood, very high self-esteem, decreased need for sleep, pressure to keep talking, racing thoughts, being easily distracted, frequently involved in activities with a large risk for bad consequences (for example, excessive buying sprees).

    Medical attention should be sought if serotonin syndrome is suspected. Please refer to serious side effects for signs/symptoms.

    Are There Specific Concerns About Desvenlafaxine And Pregnancy?
    If you are planning on becoming pregnant, notify your health care provider to best manage your medications. People living with MDD who wish to become pregnant face important decisions. Untreated MDD has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers. For women who take antidepressant medications during weeks 13 through the end of their pregnancy (second and third trimesters), there is a risk that the baby can be born before it is fully developed (before 37 weeks).

    Caution is advised with breastfeeding since desvenlafaxine does pass into breast milk.

    What Should I Discuss With My Health Care Provider Before Taking Desvenlafaxine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, including a history of bipolar disorder
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breastfeeding
    If you drink alcohol or use drugs

    How Should I Take Desvenlafaxine?
    Desvenlafaxine is usually taken one time per day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 50 mg to 400 mg. Only your healthcare provider can determine the correct dose for you.

    The tablets should be swallowed whole. They should not be chewed, crushed, or broken.

    If you are taking desvenlafaxine, you should not take other medications that include venlafaxine (Effexor®).

    Consider using a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Desvenlafaxine?
    If you miss a dose of desvenlafaxine take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your health care provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Desvenlafaxine?
    Avoid drinking alcohol or using illegal drugs while you are taking antidepressant medications. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Desvenlafaxine?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of desvenlafaxine does not exist.

    What Are The Possible Side Effects Of Desvenlafaxine?
    Common side effects

    Headache, nausea, vomiting, diarrhea, constipation, dry mouth, increased sweating, decreased appetite, tremor, feeling nervous, restless, fatigue, or having trouble sleeping (insomnia). These will often improve over the first week or two as you continue to take the medication.

    Sexual side effects, such as problems with orgasm or ejaculatory delay, and blood pressure increases often do not improve over time.

    Rare/serious side effects

    Increased heart rate, low blood pressure, increased salivation, irregular menstrual cycle, increased frequency of urination, changes in taste, increased liver enzymes, low sodium (symptoms of low sodium levels may include headache, weakness, difficulty concentrating and remembering), teeth grinding, difficulty urinating, angle closure glaucoma (symptoms of angle closure glaucoma may include eye pain, changes in vision, swelling or redness in or around eye), serotonin syndrome (symptoms may include shivering, diarrhea, confusion, severe muscle tightness, fever, seizures, and death), hypertensive crisis (severely elevated blood pressure), myocardial infarction (heart attack), Stevens-Johnson syndrome (rash)

    Are There Any Risks For Taking Desvenlafaxine For Long Periods Of Time?
    To date, there are no known problems associated with long term use of desvenlafaxine. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Desvenlafaxine?
    Desvenlafaxine should not be taken with or within 2 weeks of taking monoamine oxidase inhibitors (MAOIs). These include phenelzine (Nardil®), tranylcypromine (Parnate®), isocarboxazid (Marplan®), rasagiline (Azilect®), and selegiline (Emsam®).

    Although rare, there is an increased risk of serotonin syndrome when desvenlafaxine is used with other medications that increase serotonin, such as other antidepressants, migraine medications called “triptans” (e.g., Imitrex®), some pain medications (e.g., tramadol (Ultram®), the antibiotic linezolid (Zyvox®), and amphetamines.

    The following medication may increase the levels and effects of desvenlafaxine: ketoconazole (Nizoral®).

    Desvenlafaxine may increase the effects of other medications that can cause bleeding (e.g., ibuprofen (Advil®, Motrin®), warfarin (Coumadin®) and aspirin).

    How Long Does It Take For Desvenlafaxine To Work?
    Sleep, energy, or appetite may show some improvement within the first 1-2 weeks. Improvement in these physical symptoms can be an important early signal that the medication is working. Depressed mood and lack of interest in activities may need up to 6-8 weeks to fully improve.

    Summary Of FDA Black Box Warnings
    Suicidal thoughts or actions in children and adults

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide. Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking antidepressant medications. This risk may persist until significant remission occurs.

    In short-term studies, antidepressants increased the risk of suicidality in children, adolescents, and young adults when compared to placebo. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24. Adults age 65 and older taking antidepressants have a decreased risk of suicidality. Patients, their families, and caregivers should be alert to the emergence of anxiety, restlessness, irritability, aggressiveness and insomnia. If these symptoms emerge, they should be reported to the patient’s prescriber or health care professional. All patients being treated with antidepressants for any indication should watch for and notify their health care provider for worsening symptoms, suicidality and unusual changes in behavior, especially during the first few months of treatment.

  • Austedo (Deutetrabenazine)

    Brand name: Austedo

    Tablet: 6 mg, 9 mg, 12 mg
    Generic name: Deutetrabenazine (du tet ra BEN a zeen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Deutetrabenazine And What Does It Treat?
    Deutetrabenazine is a medication that is used to decrease the frequency and severity of involuntary, uncontrollable muscle movements that are related to a condition known as Tardive Dyskinesia (TD). TD is associated with chronic use of certain medications, such as antipsychotics. Deutetrabenazine may also be used to treat abnormal involuntary movements associated with Huntington Disease.

    Symptoms of TD include:

    Lip smacking, puckering, or pursing
    Tongue rolling or darting in and out of mouth
    Jaw clenching or grimacing
    Trunk and hip rocking, jerking, or thrusting
    Twisting or rhythmic movement in fingers and toes
    Deutetrabenazine may help improve some or all of these symptoms.

    What Is The Most Important Information I Should Know About Deutetrabenazine?
    For deutetrabenazine to work properly, it should be taken every day as prescribed by your healthcare provider. Missing doses of deutetrabenazine may increase your risk for a relapse in your symptoms.

    With input from you, your health care provider will assess how long you will need to take the medicine. Do not stop taking deutetrabenazine or change your dose without talking to your healthcare provider first.

    Are There Specific Concerns About Deutetrabenazine And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with TD who wish to become pregnant face important decisions. Currently, there are no well-controlled human studies of deutetrabenazine in pregnancy. However, increased rates of stillbirths and postnatal mortality were seen in animal studies. It is important to discuss the risk and benefits of treatment with your doctor and caregivers.

    Caution is advised with breast-feeding since it is not known if deutetrabenazine passes into your breast milk. Talk to your doctor about the best way to feed your baby during treatment with deutetrabenazine.

    What Should I Discuss With My Healthcare Provider Before Taking Deutetrabenazine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, such as depression, heart rhythm problems, long QT syndrome, heart attacks, or liver disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you drink alcohol or use illegal drugs
    How Should I Take Deutetrabenazine?
    Deutetrabenazine is usually taken twice daily, with food. Tablets should be swallowed whole; do not chew, crush or break.

    Typically patients begin at 6 mg twice a day and dose may be increased weekly in increments of 6 mg per day to a maximum of 48 mg per day (given in 2 divided doses). Only your healthcare provider can determine the correct dose for you.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Deutetrabenazine?
    If you miss a dose of deutetrabenazine, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Deutetrabenazine?
    Avoid drinking alcohol or using illegal drugs while you are taking deutetrabenazine. They may decrease the benefits (e.g. worsen your condition) and increase adverse effects (e.g. sedation) of the medication.

    What Happens If I Overdose With Deutetrabenazine?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of deutetrabenazine does not exist.

    What Are Possible Side Effects Of Deutetrabenazine?
    Common side effects

    The most common side effects of taking deutetrabenazine are inflammation of the nose and throat, fatigue, drowsiness, diarrhea, and dry mouth.

    Rare/serious side effects

    Rare/serious side effects may include insomnia, anxiety, depression, agitation, reslessness, constipation, urinary tract infection, and irregular heart rhythm.

    Are There Any Risks For Taking Deutetrabenazine For Long Periods Of Time?
    To date, there are no known problems associated with long term use of deutetrabenazine. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Deutetrabenazine?
    Deutetrabenazine should not be taken with or within 2 weeks of taking monoamine oxidase inhibitors (MAOIs) or within 20 days of taking reserpine, as these medications can increase side effects and decrease the effectiveness of deutetrabenazine. MAOIs include phenelzine (Nardil®), tranylcypromine (Parnate®), isocarboxazid (Marplan®), and selegiline (Emsam®).

    Deutetrabenazine should not be taken with tetrabenazine (Xenazine®) or yalbenazine (Ingrezza®).

    The following medications may increase the levels and effects of deutetrabenazine:

    The antidepressants paroxetine (Paxil®), fluoxetine (Prozac®), quinidine (Quinate®), and bupropion (Wellbutrin®)
    Some antiviral medications asunaprevir (Sunvepra®), darunavir (Prezista®), antibiotics such as minocycline (Minocin®)
    The following medications may decrease the levels and effects of deutetrabenazine:

    Peginterferon Alfa-2b
    Using deutetrabenazine with antipsychotics, tricyclic antidepressants, certain heart medications, and antibiotics may increase the risk of developing irregular heart rhythms.

    The risk of parkinsonism, neuroleptic malignant syndrome, and akathisia may be increased by concomitant use of deutetrabenazine and antipscyhotics.

    How Long Does It Take For Deutetrabenazine To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking deutetrabenazine. It may take several weeks to see big enough changes in your symptoms to decide if deutetrabenazine is the right medication for you.

    Summary Of FDA Black Box Warnings
    Depression and suicidal thoughts in patients with Huntington's disease

    Deutetrabenazine can increase the risk of depression and suicidal thoughts in patients with Huntington’s disease. You should consider balancing the risks of depression and suicidality with the clinical need for treatment. Patients are encouraged to report behaviors of concern to your health care provider. Caution is advised in treating patients with a history of depression or prior suicide attempts, which are increased in frequency in Huntington’s disease. Deutetrabenazine is contraindicated in patients with Huntington’s disease who are suicidal, and in patients with untreated or inadequately treated depression.

  • Valium (Diazepam)

    Brand names:

    Valium®Tablet: 2 mg, 5 mg, 10 mg
    Solution: 5 mg/mL
    Injection: 5 mg/mL (2 mL, 10 mL)
    Diastat Intensol®Liquid (concentrate): 5mg/mL
    Diastat AcuDial®Gel, rectal: 10 mg, 20 mg
    Diastat Pediatric®Gel, rectal: 2.5 mg
    Valtoco®Spray, nasal: 5 mg, 7.5 mg, 10 mg
    Generic name: diazepam (dye AZ e pam)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Diazepam And What Does It Treat?
    Diazepam is a benzodiazepine. It is approved for the treatment of anxiety, acute seizures, status epilepticus (continuous seizures), muscle spasms, alcohol withdrawal, and as a medication given right before anesthesia. This medication may be prescribed for other uses; ask your health care provider for more information.

    Symptoms of anxiety include:

    Feeling nervous
    Feeling fearful
    Excessive worrying
    Difficulty sleeping
    Difficulty concentrating
    Irritability

    What Is The Most Important Information I Should Know About Diazepam?
    Do not drive a car or operate machinery until you know how this medication affects you because you may notice that you feel tired or dizzy.

    When starting diazepam, anxiety or insomnia may improve rapidly or over a period of days.

    Benzodiazepines, such as diazepam, are often used for short periods of time only. They may produce emotional and/or physical dependence (addiction) even when used as recommended. With input from you, your health care provider will assess how long you will need to take the medicine.

    Do not stop taking diazepam without talking to your healthcare provider first. Stopping diazepam abruptly may result in one or more of the following withdrawal symptoms: irritability, nausea, tremor, dizziness, blood pressure changes, rapid heart rate, and seizures.

    The use of diazepam with drugs like opioid medications has led to serious side effects including slowed and difficulty breathing and death. Opioid drugs are medications used to treat pain and include medications such as: codeine, oxycodone, morphine, and illegal drugs like heroin. Some opioid medications are also in cough syrup.

    If you are taking diazepam with an opioid medication, get medical assistance immediately if you feel dizziness or sleepiness, if you have slow or troubled breathing, or if you pass out. Caregivers must get medical help right away if a patient does not respond and does not wake up.

    Avoid alcohol while taking this medication.

    Are There Specific Concerns About Diazepam And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with anxiety disorders who wish to become pregnant face important decisions. It is important to discuss this with your doctor and caregivers.

    Regarding breastfeeding, caution is advised since diazepam does pass into breast milk.

    What Should I Discuss With My Health Care Provider Before Taking Diazepam?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your healthcare provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have
    All other medications you are currently taking (including over the counter products and herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are elderly or prone to falls
    If you are pregnant, plan to become pregnant, or are breastfeeding
    If you drink alcohol or use drugs

    How Should I Take Diazepam?
    Diazepam may be taken with or without food.

    Diazepam may be taken every day at regular times or on an as-needed (“PRN”) basis. Typically, your healthcare provider will limit the number of doses you should take in one day.

    Your healthcare provider will determine the dose and method of taking the medication that is right for you based upon your response.

    Diazepam liquid: Measure with a dosing spoon or oral syringe, which you can get from your pharmacy.

    Diazepam nasal (Valtoco®): do not test or prime the nasal spray before you use it. Each device has only 1 spray and cannot be reused. Keep it in the box until you are ready to use it. It should be protected from light.

    If you take the medication every day (instead of “as-needed”), use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take it. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Diazepam?
    If you miss a dose of diazepam, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Diazepam?
    Avoid drinking alcohol and using illegal drugs while you are taking diazepam. They may decrease the benefits (e.g., worsen your condition) and increase the adverse effects (e.g., sedation) of the medication. Alcohol increases the risk of accidental overdose with medications like diazepam.

    What Happens If I Overdose With Diazepam?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    Symptoms of overdose include confusion, impaired coordination, slow reflexes, coma, and death.

    A specific treatment to reverse the effects of diazepam does exist. This medicine, called flumazenil, can reverse the effects of diazepam but must be given through an IV at a hospital. Only a doctor can decide if you need this medication.

    What Are The Possible Side Effects Of Diazepam?
    Common side effects

    Feeling dizzy, drowsy, fatigued, or lightheaded
    Impaired coordination, decreased ability to concentrate
    Headache, sleepiness, and nasal discomfort with diazepam nasal spray
    If you experience these side effects after starting diazepam they will often improve over the first week or two as you continue to take the medication

    Rare/serious side effects

    Increased heart rate, headache, memory impairment, irritability, and restlessness may occur.
    Some people taking benzodiazepines develop a severe allergic reaction and swelling of the face. This can occur as early as with the first dose.
    Some people taking benzodiazepines for sleep have experienced various behaviors while they were asleep/not fully awake, such as sleep driving, making phone calls, and preparing or eating food. The individuals have no memory of the events when they awaken.

    Are There Any Risks For Taking Diazepam For Long Periods Of Time?
    Diazepam is a safe and effective medication when used as directed. Benzodiazepines may produce emotional and/or physical dependence (addiction) even when used as recommended. Physical dependence may develop after 2 or more weeks of daily use.

    What Other Medications May Interact With Diazepam?
    The following medications may increase the levels and effects of diazepam:

    Ketoconazole (Nizoral®), itraconazole (Sporanox®), nefazodone (Serzone®), fluvoxamine (Luvox®), and cimetidine (Tagamet®)

    The following medications may decrease the levels and effects of diazepam:

    Carbamazepine (Tegretol®), phenytoin (Dilantin®), and phenobarbital (Luminal®)

    Diazepam should not be taken with other benzodiazepine medications.

    Diazepam may cause drowsiness, so caution should be used when combining it with other medications that cause drowsiness. These could include:

    Antihistamines such as diphenhydramine (Benadryl®)
    Narcotic pain medication such as morphine, oxycodone (OxyContin®), and hydrocodone (Vicodin® and Lortab®)
    Opioid cough medications such as codeine cough syrup
    Sleeping medications such as zolpidem (Ambien®)
    Other anti-anxiety medications, antipsychotic medications, certain anticonvulsant medications, and tricyclic antidepressant medications (such as amitriptyline)

    How Long Does It Take For Diazepam To Work?
    When starting diazepam, anxiety or insomnia may improve rapidly or over a period of days or within hours of the first dose of medication.

    Summary Of FDA Black Box Warnings
    The FDA has found that benzodiazepine drugs, such as diazepam, when used in combination with opioid medications or other sedating medications can result in serious adverse reactions including slowed or difficult breathing and death. Patients taking opioids with benzodiazepines, other sedating medications, or alcohol, and caregivers of these patients, should seek immediate medical attention if that start to experience unusual dizziness or lightheadedness, extreme sleepiness, slow or difficulty breathing, or unresponsiveness.

  • Cymbalta (Duloxetine)

    Brand names:

    Cymbalta®Capsules (delayed release): 20 mg, 30 mg, 60 mg
    Drizalma Sprinkle™Capsules (delayed release sprinkle): 20 mg, 30 mg, 40 mg, 60mg
    DuloxetineCapsules (delayed release): 20 mg, 30 mg, 40 mg, 60 mg

    Generic name: Duloxetine (doo LOX e teen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Duloxetine And What Does It Treat?
    Duloxetine is an antidepressant medication that works in the brain. It is approved for the treatment of major depressive disorder (MDD), generalized anxiety disorder (GAD), diabetic peripheral neuropathic pain (DPNP), fibromyalgia, and chronic musculoskeletal pain.

    Symptoms of depression include:

    Depressed mood - feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, and helpless
    Loss of interest or pleasure in your usual activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving and thinking in slow motion)
    Suicidal thoughts or behaviors

    Generalized Anxiety Disorder (GAD) occurs when a person experiences excessive anxiety or worry for at least six months. Other symptoms include:

    Restlessness
    Fatigue (low energy, feeling tired all the time)
    Difficulty concentrating
    Irritability
    Muscle tension
    Sleep disturbance (difficulty falling asleep or waking up in the middle of the night)

    What Is The Most Important Information I Should Know About Duloxetine?
    Do not stop taking duloxetine, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of duloxetine may increase your risk for relapse in your symptoms.

    Stopping duloxetine abruptly may result in one or more of the following withdrawal symptoms: irritability, nausea, feeling dizzy, vomiting, nightmares, headache, and/or paresthesias (prickling, tingling sensation on the skin).

    Depression is also a part of bipolar illness. People with bipolar disorder who take antidepressants may be at risk for "switching" from depression into mania. Symptoms of mania include "high" or irritable mood, very high self-esteem, decreased need for sleep, pressure to keep talking, racing thoughts, being easily distracted, frequently involved in activities with a large risk for bad consequences (for example, excessive buying sprees).

    Medical attention should be sought if serotonin syndrome is suspected. Please refer to serious side effects for signs/symptoms.

    Are There Specific Concerns About Duloxetine And Pregnancy?
    If you are planning on becoming pregnant, notify your health care provider to best manage your medications. People living with MDD who wish to become pregnant face important decisions. Untreated MDD has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers. For women who take antidepressant medications during weeks 13 through the end of their pregnancy (second and third trimesters), there is a risk that the baby can be born before it is fully developed (before 37 weeks).

    Caution is advised with breastfeeding since duloxetine does pass into breast milk.

    What Should I Discuss With My Health Care Provider Before Taking Duloxetine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes to the medication.
    Any other psychiatric or medical problems you have, including a history of bipolar disorder, kidney or liver disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breastfeeding
    If you drink alcohol or use drugs

    How Should I Take Duloxetine?
    Duloxetine is usually taken 1 or 2 times per day with or without food.

    Typically, patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 20 mg to 120 mg. Only your health care provider can determine the correct dose for you.

    The capsule should be swallowed whole. It should not be chewed, crushed, or broken.

    The duloxetine delayed release capsule (Cymbalta® or generic duloxetine) should be swallowed whole. It should not be chewed, crushed, or broken. Drizalma Sprinkle™ delayed release capsules may be opened and sprinkled on applesauce, if needed.

    Consider using a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Duloxetine?
    If you miss a dose of duloxetine take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your health care provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Duloxetine?
    Avoid drinking alcohol or using illegal drugs while you are taking antidepressant medications. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication. Alcohol increases the risk of liver problems with duloxetine.

    What Happens If I Overdose With Duloxetine?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of duloxetine does not exist.

    What Are Possible Side Effects Of Duloxetine?
    Common side effects

    Headache, nausea, diarrhea, dry mouth, decreased appetite, increased sweating, feeling nervous, restless, fatigued, sleepy or having trouble sleeping (insomnia). These will often improve over the first week or two as you continue to take the medication.

    Sexual side effects, such as problems with orgasm or ejaculatory delay, and blood pressure increases often do not improve over time.

    Rare/serious side effects

    There have been rare reports of liver failure (sometimes fatal) with duloxetine. This risk is increased in those with substantial alcohol use or chronic liver disease.

    Orthostatic hypotension, or a drop in blood pressure when standing or getting up from sleeping, has been reported in patients taking duloxetine. The risk may be greater in patients also taking medications for high blood pressure.

    Increased heart rate, irregular menstrual cycle, increased frequency of urination or difficulty urinating, increased liver enzymes, teeth grinding, low sodium (symptoms of low sodium levels may include headache, weakness, difficulty concentrating and remembering), angle closure glaucoma (symptoms of angle closure glaucoma may include eye pain, changes in vision, swelling or redness in or around eye), serotonin syndrome (symptoms may include shivering, diarrhea, confusion, severe muscle tightness, fever, seizures, and death), hypertensive crisis (severely elevated blood pressure), myocardial infarction (heart attack), Stevens-Johnson Syndrome (rash), pancreatitis

    SNRI antidepressants, including duloxetine, may increase the risk of bleeding events. Combined use of aspirin, nonsteroidal anti-inflammatory drugs (e.g., ibuprofen, naproxen), warfarin, and other anti-coagulants may increase this risk. This may include gums that bleed more easily, nose bleed, or gastrointestinal bleeding. Some cases have been life threatening.
     

    Are There Any Risks For Taking Duloxetine For Long Periods Of Time?
    To date, there are no known problems associated with long term use of duloxetine. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Duloxetine?
    Duloxetine should not be taken with or within 2 weeks of taking monoamine oxidase inhibitors (MAOIs). These include phenelzine (Nardil®), tranylcypromine (Parnate®), isocarboxazid (Marplan®), rasagiline (Azalect®) and selegiline (Emsam®).

    Although rare, there is an increased risk of serotonin syndrome when duloxetine is used with other medications that increase serotonin, such as other antidepressants, migraine medications called “triptans” (e.g., Imitrex®), some pain medications (e.g., tramadol (Ultram®), the antibiotic linezolid (Zyvox®), and amphetamines.

    The following medications may increase the levels and effects of duloxetine: cimetidine (Tagamet®), ciprofloxacin (Cipro®), fluoxetine (Prozac®), fluvoxamine (Luvox®), paroxetine (Paxil®)

    Duloxetine may increase the effects of other medications that can cause bleeding (e.g., ibuprofen (Advil®, Motrin®), warfarin (Coumadin®) and aspirin).

    How Long Does It Take For Duloxetine To Work?
    Sleep, energy, or appetite may show some improvement within the first 1-2 weeks. Improvement in these physical symptoms can be an important early signal that the medication is working. Depressed mood and lack of interest in activities may need up to 6-8 weeks to fully improve.

    Summary Of FDA Black Box Warnings
    Suicidal thoughts or actions in children and adults

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide. Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking antidepressant medications. This risk may persist until significant remission occurs.

    In short-term studies, antidepressants increased the risk of suicidality in children, adolescents, and young adults when compared to placebo. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24. Adults age 65 and older taking antidepressants have a decreased risk of suicidality. Patients, their families, and caregivers should be alert to the emergence of anxiety, restlessness, irritability, aggressiveness and insomnia. If these symptoms emerge, they should be reported to the patient’s prescriber or health care professional. All patients being treated with antidepressants for any indication should watch for and notify their health care provider for worsening symptoms, suicidality and unusual changes in behavior, especially during the first few months of treatment.

  • Lexapro (Escitalopram)

    Brand names:

    Lexapro®Tablets: 5 mg, 10 mg, 20 mg
    Liquid: 1 mg/mL
    EscitalopramTablets: 5 mg, 10 mg, 20 mg
    Liquid: 1 mg/ml

    Generic name: escitalopram (es sye TAL oh pram)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Escitalopram And What Does It Treat?
    Escitalopram is an antidepressant medication that works in the brain. It is approved for the treatment of major depressive disorder (MDD) and generalized anxiety disorder (GAD).

    Symptoms of depression include:

    Depressed mood - feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, and helpless
    Loss of interest or pleasure in your usual activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving and thinking in slow motion)
    Suicidal thoughts or behaviors

    Generalized anxiety disorder (GAD) occurs when a person experiences excessive anxiety or worry for at least six months. Other symptoms include:

    Restlessness
    Fatigue (low energy, feeling tired all the time)
    Difficulty concentrating
    Irritability
    Muscle tension
    Sleep disturbance (difficulty falling asleep or waking up in the middle of the night)

    Escitalopram may also be helpful when prescribed “off-label” for obsessive compulsive disorder (OCD), eating disorders such as binge eating disorder or bulimia nervosa, panic disorder, posttraumatic stress disorder (PTSD), and premenstrual dysphoric disorder (PMDD). “Off-label” means that it hasn’t been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an “off-label” treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Escitalopram?
    Do not stop taking escitalopram, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of escitalopram may increase your risk for relapse in your symptoms.

    Stopping escitalopram abruptly may result in one or more of the following withdrawal symptoms: irritability, nausea, feeling dizzy, vomiting, nightmares, headache, and/or paresthesias (prickling, tingling sensation on the skin).

    Depression is also a part of bipolar illness. People with bipolar disorder who take antidepressants may be at risk for "switching" from depression into mania. Symptoms of mania include "high" or irritable mood, very high self-esteem, decreased need for sleep, pressure to keep talking, racing thoughts, being easily distracted, frequently involved in activities with a large risk for bad consequences (for example, excessive buying sprees).

    Medical attention should be sought if serotonin syndrome is suspected. Please refer to serious side effects for signs/symptoms.

    Are There Specific Concerns About Escitalopram And Pregnancy?
    If you are planning on becoming pregnant, notify your health care provider to best manage your medications. People living with MDD who wish to become pregnant face important decisions. Untreated MDD has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers. For women who take antidepressant medications during weeks 13 through the end of their pregnancy (second and third trimesters), there is a risk that the baby can be born before it is fully developed (before 37 weeks).

    For mothers who have taken SSRIs during their pregnancy, there appears to be less than a 1% chance of infants developing persistent pulmonary hypertension. This is a potentially fatal condition that is associated with use of the antidepressant in the second half of pregnancy. However, women who discontinued antidepressant therapy were five times more likely to have a depression relapse than those who continued their antidepressant. If you are pregnant, please discuss the risks and benefits of antidepressant use with your health care provider.

    Caution is advised with breastfeeding since escitalopram does pass into breast milk.

    What Should I Discuss With My Health Care Provider Before Taking Escitalopram?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, including a history of bipolar disorder
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breastfeeding
    If you drink alcohol or use drugs

    How Should I Take Escitalopram?
    Escitalopram is usually taken one time per day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 10 mg to 20 mg. Only your health care provider can determine the correct dose for you.

    The liquid should be measured with a dosing spoon or oral syringe which you can get from your pharmacy.

    Consider using a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Escitalopram?
    If you miss a dose of escitalopram, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your health care provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Escitalopram?
    Avoid drinking alcohol or using illegal drugs while you are taking antidepressant medications. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Escitalopram?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of escitalopram does not exist.

    What Are The Possible Side Effects Of Escitalopram?
    Common side effects

    Headache, nausea, diarrhea, dry mouth, increased sweating, feeling nervous, restless, fatigue, or having trouble sleeping (insomnia). These will often improve over the first week or two as you continue to take the medication.

    Sexual side effects, such as problems with orgasm or ejaculatory delay often do not diminish over time.

    Rare/serious side effects

    Low sodium blood levels (symptoms of low sodium levels may include headache, weakness, difficulty concentrating and remembering), teeth grinding, angle closure glaucoma (symptoms of angle closure glaucoma may include eye pain, changes in vision, swelling or redness in or around eye), serotonin syndrome (symptoms may include shivering, diarrhea, confusion, severe muscle tightness, fever, seizures, and death), seizure

    SSRI antidepressants including escitalopram may increase the risk of bleeding events. Combined use of aspirin, nonsteroidal anti-inflammatory drugs (e.g., ibuprofen, naproxen), warfarin, and other anti-coagulants may increase this risk. This may include symptoms such as gums that bleed more easily, nose bleed, or gastrointestinal bleeding. Some cases have been life threatening.

    Are There Any Risks For Taking Escitalopram For Long Periods Of Time?
    To date, there are no known problems associated with long term use of escitalopram. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Escitalopram?
    Escitalopram should not be taken with or within 2 weeks of taking monoamine oxidase inhibitors (MAOIs). These include phenelzine (Nardil®), tranylcypromine (Parnate®), isocarboxazid (Marplan®), rasagiline (Azilect®), and selegiline (Emsam®).

    Although rare, there is an increased risk of serotonin syndrome when escitalopram is used with other medications that increase serotonin, such as other antidepressants, migraine medications called “triptans” (e.g., Imitrex®), some pain medications (e.g., tramadol (Ultram®), the antibiotic linezolid (Zyvox®), and amphetamines.

    Escitalopram may increase the effects of other medications that can cause bleeding (e.g., ibuprofen (Advil®, Motrin®), warfarin (Coumadin®) and aspirin).

    How Long Does It Take For Escitalopram To Work?
    Sleep, energy, or appetite may show some improvement within the first 1-2 weeks. Improvement in these physical symptoms can be an important early signal that the medication is working. Depressed mood and lack of interest in activities may need up to 6-8 weeks to fully improve.

    Summary Of FDA Black Box Warnings
    Suicidal thoughts or actions in children and adults

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide. Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking antidepressant medications. This risk may persist until significant remission occurs.

    In short-term studies, antidepressants increased the risk of suicidality in children, adolescents, and young adults when compared to placebo. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24. Adults age 65 and older taking antidepressants have a decreased risk of suicidality. Patients, their families, and caregivers should be alert to the emergence of anxiety, restlessness, irritability, aggressiveness and insomnia. If these symptoms emerge, they should be reported to the patient’s prescriber or health care professional. All patients being treated with antidepressants for any indication should watch for and notify their health care provider for worsening symptoms, suicidality and unusual changes in behavior, especially during the first few months of treatment.

  • Prozac (Fluoxetine)

    Brand names:

    Prozac®Capsules: 10 mg, 20 mg, 40 mg
    Prozac Weekly®Capsules (delayed-release): 90 mg
    Sarafem®Tablets: 10 mg, 20 mg
    FluoxetineCapsules: 10 mg, 20 mg, 40 mg
    Capsules (delayed release): 90 mg
    Liquid: 20 mg/5ml
    Tablets: 10 mg, 20 mg, 60 mg

    Generic name: Fluoxetine (floo OKS e teen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Fluoxetine And What Does It Treat?
    Fluoxetine is an antidepressant medication that works in the brain. It is approved for the treatment of major depressive disorder (MDD), obsessive compulsive disorder (OCD), panic disorder, bulimia nervosa, and premenstrual dysphoric disorder (PMDD).

    Symptoms of depression include:

    Depressed mood - feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, and helpless
    Loss of interest or pleasure in your usual activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving and thinking in slow motion)
    Suicidal thoughts or behaviors

    Obsessive compulsive disorder (OCD) occurs when a person experiences the following symptoms at the same time:

    Obsessions (unwanted, recurrent, and disturbing thoughts)
    Compulsions (repetitive, ritualized behaviors that the person feels driven to perform in order to lessen the anxiety produced by the obsessions)

    Panic disorder occurs when a person experiences unexpected and repeated episodes of intense fear. These episodes have physical symptoms including chest pain, shortness of breath, heart palpitations, sweating, dizziness, and nausea. Fear of future episodes is also part of panic disorder.

    Bulimia is a condition where a person binges on food, then uses various methods to purge (e.g., use of laxatives, vomiting) in order to prevent weight gain.

    Premenstrual dysphoric disorder (PMDD) is a condition where a woman experiences depression, tension, and irritability for a few days prior to menstruation that end when menstruation begins. These symptoms are more severe than those of premenstrual syndrome (PMS).

    Fluoxetine may also be helpful when prescribed “off-label” for body dysmorphic disorder, binge eating disorder, generalized anxiety disorder (GAD), social phobia (also known as social anxiety disorder), dysthymia, or posttraumatic stress disorder (PTSD). “Off-label” means that it hasn’t been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an “off-label” treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Fluoxetine?
    Do not stop taking fluoxetine, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of fluoxetine may increase your risk for relapse in your symptoms.

    Stopping fluoxetine abruptly may result in one or more of the following withdrawal symptoms: irritability, nausea, dizziness, vomiting, nightmares, headache, and/or paresthesias (prickling, tingling sensation on the skin).

    Depression is also a part of bipolar illness. People with bipolar disorder who take antidepressants may be at risk for "switching" from depression into mania. Symptoms of mania include "high" or irritable mood, very high self-esteem, decreased need for sleep, pressure to keep talking, racing thoughts, being easily distracted, frequently involved in activities with a large risk for bad consequences (for example, excessive buying sprees).

    Medical attention should be sought if serotonin syndrome is suspected. Please refer to serious side effects for signs/symptoms.

    Are There Specific Concerns About Fluoxetine And Pregnancy?
    If you are planning on becoming pregnant, notify your health care provider to best manage your medications. People living with MDD who wish to become pregnant face important decisions. Untreated MDD has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers. For women who take antidepressant medications during weeks 13 through the end of their pregnancy (second and third trimesters), there is a risk that the baby can be born before it is fully developed (before 37 weeks).

    For mothers who have taken SSRIs during their pregnancy, there appears to be less than a 1% chance of infants developing persistent pulmonary hypertension. This is a potentially fatal condition that is associated with use of the antidepressant in the second half of pregnancy. However, women who discontinued antidepressant therapy were five times more likely to have a depression relapse than those who continued their antidepressant. If you are pregnant, please discuss the risks and benefits of antidepressant use with your health care provider.

    Caution is advised with breastfeeding since fluoxetine does pass into breast milk.

    What Should I Discuss With My Health Care Provider Before Taking Fluoxetine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, including a history of bipolar disorder
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breastfeeding
    If you drink alcohol or use drugs

    How Should I Take Fluoxetine?
    Fluoxetine is usually taken one time per day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 20 mg to 80 mg when taken once daily or 90 mg taken once weekly. Only your health care provider can determine the correct dose for you.

    If you are taking fluoxetine for PMDD, it can be taken once daily (everyday) or intermittently (usually starting 14 days prior to menstruation through the first full day of menses of each cycle). Discuss this with your prescriber.

    The liquid should be measured with a dosing spoon or oral syringe which you can get from your pharmacy.

    The delayed release form should be swallowed whole. It should not be chewed, crushed, or broken.

    Consider using a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Fluoxetine?
    If you miss a dose of fluoxetine that you take daily, take it as soon as you remember, unless it is closer to the time of your next dose. If you take fluoxetine once weekly, take it as soon as possible, then go back to your regular schedule the next week. Discuss this with your health care provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Fluoxetine?
    Avoid drinking alcohol or using illegal drugs while you are taking antidepressant medications. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Fluoxetine?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of fluoxetine does not exist.

    What Are The Possible Side Effects Of Fluoxetine?
    Common side effects

    Headache, nausea, diarrhea, dry mouth, increased sweating, feeling nervous, restless, fatigue, or having trouble sleeping (insomnia). These will often improve over the first week or two as you continue to take the medication.

    Sexual side effects, such as problems with orgasm or ejaculatory delay often do not diminish over time.

    Rare/serious side effects

    Low sodium blood levels (symptoms of low sodium levels may include headache, weakness, difficulty concentrating and remembering), teeth grinding, angle closure glaucoma (symptoms of angle closure glaucoma may include eye pain, changes in vision, swelling or redness in or around eye), serotonin syndrome (symptoms may include shivering, diarrhea, confusion, severe muscle tightness, fever, seizures, and death), seizure, QT prolongation and ventricular arrhythmia including Torsades de Pointes (changes in the electrical activity of your heart; symptoms may include fast, slow or irregular heartbeat, shortness of breath, and dizziness or fainting)

    SSRI antidepressants including fluoxetine may increase the risk of bleeding events. Combined use of aspirin, nonsteroidal anti-inflammatory drugs (e.g., ibuprofen, naproxen), warfarin, and other anti-coagulants may increase this risk. This may include symptoms such as gums that bleed more easily, nose bleed, or gastrointestinal bleeding. Some cases have been life threatening.

    Are There Any Risks For Taking Fluoxetine For Long Periods Of Time?
    To date, there are no known problems associated with long term use of fluoxetine. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Fluoxetine?
    Fluoxetine should not be taken with or within 6 weeks of taking monoamine oxidase inhibitors (MAOIs). These include phenelzine (Nardil®), tranylcypromine (Parnate®), isocarboxazid (Marplan®), rasagiline (Azilect®), and selegiline (Emsam®).

    Although rare, there is an increased risk of serotonin syndrome when fluoxetine is used with other medications that increase serotonin, such as other antidepressants, migraine medications called “triptans” (e.g., Imitrex®), some pain medications (e.g., tramadol (Ultram®), amphetamines, and the antibiotic linezolid (Zyvox®).

    Fluoxetine may increase the levels and effects of:

    Certain anticonvulsants, such as phenytoin (Dilantin®), carbamazepine (Tegretol®, Equetro®)
    Certain antipsychotics, such as haloperidol (Haldol®), aripiprazole (Abilify®)
    Benzodiazepines, such as alprazolam (Xanax®), diazepam (Valium®)
    Atomoxetine (Straterra®)
    Warfarin (Coumadin®)
    Metoclopramide (Reglan®)
    Tricyclic antidepressants, such as imipramine (Tofranil®), desipramine (Norpramin®)
    Beta blockers, such as metoprolol (Toprol XL®, Lopressor®) and propranolol (Inderal®)
    Fluoxetine may decrease the effects of tamoxifen (Nolvadex®) and codeine.

    Fluoxetine may increase the effects of other medications that can cause bleeding (e.g., ibuprofen (Advil®, Motrin®), warfarin (Coumadin®), and aspirin).

    How Long Does It Take For Fluoxetine To Work?
    Sleep, energy, or appetite may show some improvement within the first 1-2 weeks. Improvement in these physical symptoms can be an important early signal that the medication is working. Depressed mood and lack of interest in activities may need up to 6-8 weeks to fully improve.

    Summary Of FDA Black Box Warnings
    Suicidal thoughts or actions in children and adults

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide. Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking antidepressant medications. This risk may persist until significant remission occurs.

    In short-term studies, antidepressants increased the risk of suicidality in children, adolescents, and young adults when compared to placebo. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24. Adults age 65 and older taking antidepressants have a decreased risk of suicidality. Patients, their families, and caregivers should be alert to the emergence of anxiety, restlessness, irritability, aggressiveness and insomnia. If these symptoms emerge, they should be reported to the patient’s prescriber or health care professional. All patients being treated with antidepressants for any indication should watch for and notify their health care provider for worsening symptoms, suicidality and unusual changes in behavior, especially during the first few months of treatment.

  • Luvox (Fluvoxamine)

    Brand names:

    Luvox®Tablets (immediate release): 25 mg, 50 mg, 100 mg
    Luvox CR®Capsules (extended release): 100 mg, 150 mg

    Generic name: fluvoxamine (floo VOKS a meen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Fluvoxamine And What Does It Treat?
    Fluvoxamine is an antidepressant medication that works in the brain. It is approved for the treatment of obsessive compulsive disorder (OCD) in adults and children ages 8 and older.

    Obsessive Compulsive Disorder (OCD) occurs when a person experiences the following symptoms at the same time:

    Obsessions (unwanted, recurrent, and disturbing thoughts)
    Compulsions (repetitive, ritualized behaviors that the person feels driven to perform in order to lessen the anxiety produced by the obsessions)

    Fluvoxamine may also be helpful when prescribed “off-label” for major depressive disorder (MDD), social phobia (also known as social anxiety disorder), posttraumatic stress disorder (PTSD), panic disorder, and eating disorders including bulimia nervosa and binge-eating disorder. “Off-label” means that it hasn’t been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an “off-label” treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    Symptoms of depression include:

    Depressed mood - feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, and helpless
    Loss of interest or pleasure in your usual activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving and thinking in slow motion)
    Suicidal thoughts or behaviors

    Social phobia (also known as social anxiety disorder) is a fear of situations where one may feel as if they are being judged by others. Symptoms include:

    Blushing
    Difficulty talking
    Nausea
    Sweating
    Shaking

    What Is The Most Important Information I Should Know About Fluvoxamine?
    Do not stop taking fluvoxamine, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of fluvoxamine may increase your risk for relapse in your symptoms.

    Stopping fluvoxamine abruptly may result in one or more of the following withdrawal symptoms: irritability, nausea, dizziness, vomiting, nightmares, headache, and/or paresthesias (prickling, tingling sensation on the skin).

    Depression is also a part of bipolar illness. People with bipolar disorder who take antidepressants may be at risk for "switching" from depression into mania. Symptoms of mania include "high" or irritable mood, very high self-esteem, decreased need for sleep, pressure to keep talking, racing thoughts, being easily distracted, frequently involved in activities with a large risk for bad consequences (for example, excessive buying sprees).

    Medical attention should be sought if serotonin syndrome is suspected. Please refer to serious side effects for signs/symptoms.

    Are There Specific Concerns About Fluvoxamine And Pregnancy?
    If you are planning on becoming pregnant, notify your health care provider to best manage your medications. People living with MDD who wish to become pregnant face important decisions. Untreated MDD has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers. For women who take antidepressant medications during weeks 13 through the end of their pregnancy (second and third trimesters), there is a risk that the baby can be born before it is fully developed (before 37 weeks).

    For mothers who have taken SSRIs during their pregnancy, there appears to be less than a 1% chance of infants developing persistent pulmonary hypertension. This is a potentially fatal condition that is associated with use of the antidepressant in the second half of pregnancy. However, women who discontinued antidepressant therapy were five times more likely to have a depression relapse than those who continued their antidepressant. If you are pregnant, please discuss the risks and benefits of antidepressant use with your health care provider.

    Caution is advised with breastfeeding since fluvoxamine does pass into breast milk.

    What Should I Discuss With My Health Care Provider Before Taking Fluvoxamine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, including a history of bipolar disorder
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breastfeeding
    If you drink alcohol or use drugs

    How Should I Take Fluvoxamine?
    Fluvoxamine is usually taken two times per day with or without food. The extended release formulation may be taken one time per day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 50 mg to 300 mg. Only your health care provider can determine the correct dose for you.

    Consider using a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or friend to remind you or check in with you to be sure you are taking your medication.

    The extended-release forms should be swallowed whole. They should not be chewed, crushed, or broken.

    What Happens If I Miss A Dose Of Fluvoxamine?
    If you miss a dose of fluvoxamine, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your health care provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Fluvoxamine?
    Avoid drinking alcohol or using illegal drugs while you are taking antidepressant medications. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Fluvoxamine?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of fluvoxamine does not exist.

    What Are The Possible Side Effects Of Fluvoxamine?
    Common side effects

    Headache, nausea, diarrhea, dry mouth, dizziness, increased sweating, feeling nervous, restless, fatigued, or having trouble sleeping (insomnia). These will often improve over the first week or two as you continue to take the medication.

    Sexual side effects, such as problems with orgasm or ejaculatory delay, often do not diminish over time.

    Rare/serious side effects

    Low sodium blood levels (symptoms of low sodium levels may include headache, weakness, difficulty concentrating and remembering), teeth grinding, angle closure glaucoma (symptoms of angle closure glaucoma may include eye pain, changes in vision, swelling or redness in or around eye), serotonin syndrome (symptoms may include shivering, diarrhea, confusion, severe muscle tightness, fever, seizures, and death), seizure

    SSRI antidepressants including fluvoxamine may increase the risk of bleeding events. Combined use of aspirin, nonsteroidal anti-inflammatory drugs (e.g., ibuprofen, naproxen), warfarin, and other anti-coagulants may increase this risk. This may include symptoms such as gums that bleed more easily, nose bleed, or gastrointestinal bleeding. Some cases have been life threatening.

    Are There Any Risks For Taking Fluvoxamine For Long Periods Of Time?
    To date, there are no known problems associated with long term use of fluvoxamine. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Fluvoxamine?
    Fluvoxamine should not be taken with or within 6 weeks of taking monoamine oxidase inhibitors (MAOIs). These include phenelzine (Nardil®), tranylcypromine (Parnate®), isocarboxazid (Marplan®), rasagiline (Azilect®), and selegiline (Emsam®).

    Although rare, there is an increased risk of serotonin syndrome when fluvoxamine is used with other medications that increase serotonin, such as other antidepressants, migraine medications called “triptans” (e.g., Imitrex®), some pain medications (e.g., tramadol (Ultram®), amphetamines, and the antibiotic linezolid (Zyvox®).

    Fluvoxamine may increase the levels and effects of:

    Warfarin (Coumadin®)
    Theophylline (Theo-Dur®)
    Certain anticonvulsants: carbamazepine (Tegretol®, Equetro®), phenytoin (Dilantin®)
    Beta blockers, such as propranolol (Inderal®), metoprolol (Lopressor®, Toprol XL®)
    Benzodizapines, such as alprazolam (Xanax®), diazepam (Valium®)
    Certain antipsychotics, such as olanzapine (Zyprexa®), clozapine (Clozaril®), aripiprazole (Abilify®), quetiapine (Seroquel®)
    Mexiletine (Mexitil®)
    Omeprazole (Prilosec®)
    Methadone (Dolophine®)
    Tricyclic antidepressants, such as amitriptyline (Elavil®)
    Warfarin (Coumadin®)
    Theophylline (Theo-Dur®)
    Certain anticonvulsants: carbamazepine (Tegretol®, Equetro®), phenytoin (Dilantin®)
    Beta blockers, such as propranolol (Inderal®), metoprolol (Lopressor®, Toprol XL®)
    Benzodizapines, such as alprazolam (Xanax®), diazepam (Valium®)
    Certain antipsychotics, such as olanzapine (Zyprexa®), clozapine (Clozaril®), aripiprazole (Abilify®), quetiapine (Seroquel®)
    Mexiletine (Mexitil®)
    Omeprazole (Prilosec®)
    Methadone (Dolophine®)
    Tricyclic antidepressants, such as amitriptyline (Elavil®)

    Fluvoxamine may decrease the effects of clopidogrel (Plavix®).

    Fluvoxamine may increase the effects of other medications that can cause bleeding (e.g., ibuprofen (Advil®, Motrin®), warfarin (Coumadin®), and aspirin).

    Combining fluvoxamine with ramelteon (RozeremTM), tizanidine (Zanaflex®), thioridazine (Mellaril®), pimozide, or alosetron (Lotronex®) is not recommended.

    How Long Does It Take For Fluvoxamine To Work?
    Sleep, energy, or appetite may show some improvement within the first 1-2 weeks. Improvement in these physical symptoms can be an important early signal that the medication is working. Depressed mood and lack of interest in activities may need up to 6-8 weeks to fully improve.

    Summary Of FDA Black Box Warnings
    Suicidal thoughts or actions in children and adults

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide. Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking antidepressant medications. This risk may persist until significant remission occurs.

    In short-term studies, antidepressants increased the risk of suicidality in children, adolescents, and young adults when compared to placebo. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24. Adults age 65 and older taking antidepressants have a decreased risk of suicidality. Patients, their families, and caregivers should be alert to the emergence of anxiety, restlessness, irritability, aggressiveness and insomnia. If these symptoms emerge, they should be reported to the patient’s prescriber or health care professional. All patients being treated with antidepressants for any indication should watch for and notify their health care provider for worsening symptoms, suicidality and unusual changes in behavior, especially during the first few months of treatment.

  • Intuniv (Guanfacine)

    Brand names:

    Intuniv®Tablet (extended release): 1 mg, 2 mg, 3 mg, 4 mg
    Tenex®Tablet (immediate release): 1 mg, 2 mg
    Generic name: guanfacine (GWAHN fa seen)

    All FDA black box warnings are at the end of this fact sheet. Please consult them before taking this medication.

    What Is Guanfacine And What Does It Treat?
    Guanfacine is a prescription medication that is used to treat attention-deficit hyperactivity disorder (ADHD) in individuals between 6 and 17 years of age. Guanfacine is also used to treat blood pressure in both children and adults.

    Symptoms of ADHD interfere with an individual’s ability to function at school or work or in social settings and include:

    Inattention (e.g., making careless mistakes, losing things necessary for tasks)
    Hyperactivity (e.g., inability to sit still)
    Impulsivity (e.g., interrupting or intruding on others)
    A person may have severe inattention without hyperactivity or impulsivity.

    Guanfacine is used in addition to non-medication treatments to manage ADHD symptoms.

    What Is The Most Important Information I Should Know About Guanfacine?
    Although some symptoms may improve within days of starting guanfacine, it may take several weeks before you notice the full benefits of the medication.

    Are There Specific Concerns About Guanfacine And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider so that he/she can best manage your medications. People living with ADHD who wish to become pregnant face important decisions. There are no well-controlled studies of guanfacine use in pregnant women. Animal studies did not demonstrate evidence of fetal harm. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Regarding breastfeeding, caution is advised since guanfacine does pass into breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Guanfacine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    If you experience side effects from your medications, discuss them with your provider. Some side effects pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, including heart disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you drink alcohol or use drugs
    How Should I Take Guanfacine?
    Guanfacine is usually taken one to two times per day. Guanfacine can be taken with or without food. However, taking it with a high fat meal can increase absorption and may increase exposure.

    The dose usually ranges from 1 mg to 4 mg per day. Only your health care provider can determine the correct dose for you.

    Extended release tablets (Intuniv) should not be crushed, chewed or divided. Swallow the tablet whole.

    What Happens If I Miss A Dose Of Guanfacine?
    If you miss a dose of guanfacine take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Guanfacine?
    Guanfacine may cause dizziness or drowsiness, especially when first starting the medication. Make sure you know how you react to the medication before you drive, operate machinery, or participate in other activities that may be dangerous if you are not alert.

    Avoid drinking alcohol or using illegal drugs while you are taking this medication. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Guanfacine?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    Overdosing with guanfacine may cause sleepiness, dizziness, low blood pressure and slow heart rate.

    A specific treatment to reverse the effects of guanfacine does not exist.

    What Are Possible Side Effects Of Guanfacine?
    Common side effects

    Sleepiness, drowsiness, dizziness, headache, irritability
    Low blood pressure
    Nausea, stomach pain, dry mouth, constipation and decreased appetite
    Rare/serious side effects

    Very low blood pressure or heart rate
    Fainting
    Are There Any Risks For Taking Guanfacine For Long Periods Of Time?
    There are no known problems associated with long term use of guanfacine.

    What Other Medications May Interact With Guanfacine?
    The following medications may increase the levels and effects of guanfacine:

    Increased levels: ketoconazole (Nizoral®)
    Increased effects:Medications that lower blood pressure or cause sedation (sleepiness)
    Other products containing guanfacine or clonidine (Catapres® or Kapvay®)
    The following medications may decrease the levels and effects of guanfacine: rifampin (Rifadin®), carbamazepine (Tegretol®), and phenytoin (Dilantin®)

    Guanfacine may increase the levels and effects of: valproic acid (Depakene®, Depakote®, Depakote-ER®, Stavzor®)

    How Long Does It Take For Guanfacine To Work?
    It may take four to eight weeks to get the maximum benefit once the right dose is determined. However, improvements in some symptoms may occur sooner.

    Summary Of FDA Black Box Warnings
    There are no FDA black box warnings for guanfacine.

  • Haldol (Haloperidol)

    Brand name: Haldol®

    Tablet: 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg, 20 mg
    Oral solution: 2 mg/mL
    Short-acting injection: 5 mg/mL
    Long-acting injection (Haldol decanoate): 50 mg/mL, 100 mg/mL
    Generic name: haloperidol (HAL oh PER i dol)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Haloperidol And What Does It Treat?
    Haloperidol is a medication that works in the brain to treat schizophrenia. It is also known as a first generation antipsychotic (FGA) or typical antipsychotic. Haloperidol rebalances dopamine to improve thinking, mood, and behavior.

    Symptoms of schizophrenia include:

    Hallucinations — imagined voices or images that seem real
    Delusions — beliefs that are not true (e.g., other people are reading your thoughts)
    Disorganized thinking or trouble organizing your thoughts and making sense
    Little desire to be around other people
    Trouble speaking clearly
    Lack of motivation
    Haloperidol may help some or all of these symptoms.

    Haloperidol is also FDA approved for Tourette syndrome as well as hyperactive behavior or severe behavioral problems in children that do not respond to therapy or other medications.

    What Is The Most Important Information I Should Know About Haloperidol?
    Schizophrenia requires long-term treatment. Do not stop taking haloperidol, even when you feel better.

    With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of haloperidol may increase your risk for a relapse in your symptoms.

    Do not stop taking haloperidol or change your dose without talking to with your healthcare provider first.

    For haloperidol to work properly, it should be taken every day as ordered by your healthcare provider.

    Are There Specific Concerns About Haloperidol And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with schizophrenia who wish to become pregnant face important decisions. This is a complex decision since untreated schizophrenia has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Antipsychotic use during the third trimester of pregnancy has a risk for abnormal muscle movements (extrapyramidal symptoms [EPS]) and/or withdrawal symptoms in newborns following delivery. Symptoms in the newborn may include agitation, feeding disorder, hypertonia, hypotonia, respiratory distress, somnolence, and tremor; these effects may be self-limiting or require hospitalization.

    Caution is advised with breastfeeding since haloperidol does pass into breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Haloperidol?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you ever had muscle stiffness, shaking, tardive dyskinesia, neuroleptic malignant syndrome, or weight gain caused by a medication
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any psychiatric or medical problems you have, such as heart rhythm problems, long QT syndrome, heart attacks, diabetes, high cholesterol, or seizures
    If you have a family history of diabetes or heart disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you smoke, drink alcohol, or use illegal drugs
    How Should I Take Haloperidol?
    Haloperidol tablets and solution are usually taken 1 or 2 times per day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose of the oral medication usually ranges from 5 mg to 20 mg. The dose of the long-acting injection is 25 mg to 200 mg. Only your healthcare provider can determine the correct dose for you.

    Haloperidol oral solution should be measured with a dosing spoon or oral syringe, which you can get from your pharmacy if one is not provided with the product.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    The long-acting injection form of haloperidol is administered every 3 to 4 weeks. Your healthcare provider will administer these injections.

    What Happens If I Miss A Dose Of Haloperidol?
    If you miss a dose of haloperidol, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Haloperidol?
    Avoid drinking alcohol or using illegal drugs while you are taking haloperidol. They may decrease the benefits (e.g. worsen your confusion) and increase adverse effects (e.g. sedation) of the medication.

    What Happens If I Overdose With Haloperidol?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of haloperidol does not exist.

    What Are Possible Side Effects Of Haloperidol?
    Common side effects

    Rapid heartbeat, constipation, blurry vision, dry mouth, drop in blood pressure upon standing

    Feeling drowsy, dizzy, or restless

    Patients receiving haloperidol decanoate long-acting injection may notice some pain at the site of the injection. This pain should resolve after a few days.

    Rare/serious side effects

    Haloperidol may increase the blood levels of a hormone called prolactin. Side effects of increased prolactin levels include females losing their period, production of breast milk and males losing their sex drive or possibly experiencing erectile problems. Long term (months or years) of elevated prolactin can lead to osteoporosis or increased risk of bone fractures.

    Some people may develop muscle related side effects while taking haloperidol. The technical terms for these are “extrapyramidal symptoms” (EPS) and “tardive dyskinesia” (TD). Symptoms of EPS include restlessness, tremor, and stiffness. TD symptoms include slow or jerky movements that one cannot control, often starting in the mouth with tongue rolling or chewing movements.

    Temperature regulation: Impaired core body temperature regulation may occur; caution with strenuous exercise, heat exposure, and dehydration.

    All antipsychotics have been associated with the risk of sudden cardiac death due to an arrhythmia (irregular heart beat). To minimize this risk, antipsychotic medications should be used in the smallest effective dose when the benefits outweigh the risks. Your doctor may order an EKG to monitor for irregular heartbeat.

    Neuroleptic malignant syndrome is a rare, life threatening adverse effect of antipsychotics which occurs in

    All antipsychotics can cause sedation, dizziness, or orthostatic hypotension (a drop in blood pressure when standing up from sitting or lying down). These side effects may lead to falls which could cause bone fractures or other injuries. This risk is higher for people with conditions or other medications that could worsen these effects. If falls or any of these symptoms occur, contact your healthcare provider.

    Are There Any Risks For Taking Haloperidol For Long Periods Of Time?
    Tardive dyskinesia (TD) is a side effect that develops with prolonged use of antipsychotics. If you develop symptoms of TD, such as grimacing, sucking, and smacking of lips, or other movements that you cannot control, contact your healthcare provider immediately. All patients taking either first or second generation antipsychotics should have an Abnormal Involuntary Movement Scale (AIMS) completed regularly by their healthcare provider to monitor for TD.

    What Other Medications May Interact With Haloperidol?
    Haloperidol may block the effects of agents used to treat Parkinson’s disease such as levodopa/carbidopa (Sinemet®), bromocriptine, pramipexole (Mirapex®), ropinirole (Requip®), and others.

    Haloperidol may lower your blood pressure. Medications used to lower blood pressure may increase this effect and increase your risk of falling. Propranolol (Inderal®) is an example of this type of medication.

    The following medications may increase the risk of heart problems when used with haloperidol:

    Antipsychotics including chlorpromazine (Thorazine®), thioridizine (Mellaril®), iloperidone (Fanapt®), paliperidone (Invega®), pimozide (Orap®), quetiapine (Seroquel®), and ziprasidone (Geodon®).
    Antiarrhythmics (heart rhythm medications) including procainamide, quinidine, amiodarone (Cordarone®), dronedarone (Multaq®), and sotalol (Betapace®).
    Metoclopramide (Reglan®) may increase the risk of EPS or TD when used in combination with haloperidol.

    The following medications may increase the levels and effects of haloperidol: bupropion (Wellbutrin®), fluoxetine (Prozac®), fluvoxamine (Luvox®), ketoconazole (Nizoral®),venlafaxine (Effexor®), and paroxetine (Paxil®).

    The following medications may decrease the levels and effects of haloperidol: carbamazepine (Tegretol®, Equatro®), phenytoin (Dilantin®), phenobarbital, and rifampin (Rifadin®)

    How Long Does It Take For Haloperidol To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking haloperidol. It will probably take several weeks to see big enough changes in your symptoms to decide if haloperidol is the right medication for you.

    Antipsychotic treatment is generally needed lifelong for persons with schizophrenia. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Hallucinations, disorganized thinking, and delusions may improve in the first 1-2 weeks
    Sometimes these symptoms do not completely go away
    Motivation and desire to be around other people can take at least 1-2 weeks to improve
    Symptoms continue to get better the longer you take haloperidol
    It may take 2-3 months before you get the full benefit of haloperidol


    Summary Of FDA Black Box Warnings
    Increased mortality in elderly patients with dementia-related psychosis

    Both first generation (typical) and second generation (atypical) antipsychotics are associated with an increased risk of mortality in elderly patients when used for dementia related psychosis.
    Although there were multiple causes of death in studies, most deaths appeared to be due to cardiovascular causes (e.g. sudden cardiac death) or infection (e.g. pneumonia).
    Antipsychotics are not indicated for the treatment of dementia-related psychosis.

  • Vistaril, Atarax (Hydroxyzine)

    Brand names:

    Vistaril®Capsule: 25 mg, 50 mg
    Liquid: 25 mg/5 ml suspension
    Atarax®Tablet: 10 mg, 25 mg, 50 mg
    Liquid: 10 mg/5 ml
    Injection: 25 mg/ml, 50 mg/ml
    Generic name: hydroxyzine (hye DROKS i zeen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Hydroxyzine And What Does It Treat?
    Hydroxyzine is an antihistamine. It is approved for the treatment of anxiety. However, hydroxyzine is also used to treat difficulty sleeping, nausea, itching, and allergies.

    Symptoms of anxiety include:

    Feeling nervous
    Feeling fearful
    Excessive worrying
    Difficulty sleeping
    Difficulty concentrating
    Irritability
    What Is The Most Important Information I Should Know About Hydroxyzine?
    Do not drive a car or operate machinery until you know how this medication affects you because you may notice that you feel tired or dizzy.

    Hydroxyzine is not a controlled substance. It does not have the risk of addiction like some other medications used to treat anxiety (e.g., Ativan® (lorazepam)).

    Are There Specific Concerns About Hydroxyzine And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with anxiety disorders who wish to become pregnant face important decisions. It is important to discuss this with your doctor and caregivers.

    Hydroxyzine should not be used in the first trimester of pregnancy. Studies that were done with mice and rats found an increased risk of birth defects. The risk to humans in the first trimester is unclear. Hydroxyzine may be used in the second and third trimesters of pregnancy, but it should not be used during or just prior to labor. Use of hydroxyzine during labor may increase seizure risk in infants, decrease fetal heart rate, and increase side effects when combined with narcotics.

    Regarding breast-feeding, use is not recommended since hydroxyzine does pass into breast milk. Infants who have received other antihistamines have experienced drowsiness, irritability, or unusual excitement. In addition, it may lower milk production in the mother.

    What Should I Discuss With My Healthcare Provider Before Taking Hydroxyzine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your healthcare provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, including obstructive sleep apnea
    All other medications you are currently taking (including over the counter products and herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication
    If you are elderly or are prone to falls
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you drink alcohol or use drugs
    How Should I Take Hydroxyzine?
    Hydroxyzine may be taken with or without food. Take with food if you experience an upset stomach.

    Hydroxyzine may be taken every day at regular times or on an as needed (“PRN”) basis. Typically, your healthcare provider will limit the number of doses you should take in one day.

    Your healthcare provider will determine the dose and method of taking the medication that is right for you based upon your response.

    If you take the medication every day (instead of ‘as needed’), use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take it. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Hydroxyzine?
    If you miss a dose of hydroxyzine, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Hydroxyzine?
    Avoid drinking alcohol and using illegal drugs while you are taking hydroxyzine. They may decrease the benefits (e.g., worsen your condition) and increase the adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Hydroxyzine?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    Symptoms of overdose include severe drowsiness, dry mouth, difficulty urinating, headache, rapid heartbeat, confusion, impaired coordination, slow reflexes, seizures, or coma.

    A specific treatment to reverse the effects of hydroxyzine does not exist.

    What Are Possible Side Effects Of Hydroxyzine?
    Common side effects

    Dizziness, drowsiness, fatigue, dry mouth
    Urinary retention, blurred vision, confusion, irritability
    Headache

    Rare/serious side effects

    Allergic reaction (difficulty breathing; hives; swelling of your lips, tongue or face)
    Increased heart rate, unsafe heart beat (long QT on ECG), confusion, hallucinations
    Priapism (an erection in males that does not go away after 4 hours)
    Are There Any Risks For Taking Hydroxyzine For Long Periods Of Time?
    To date, there are no known problems associated with the long-term use of hydroxyzine. It is a safe and effective medication when used as directed.

    Physician should reassess periodically the usefulness of the drug for the individual patient.

    What Other Medications May Interact With Hydroxyzine?
    The following medications may increase the levels and effects of hydroxyzine:

    Other antihistamines, such as diphenhydramine (Benadryl®) and cetirizine (Zyrtec®)
    Other medications with anticholinergic effects, such as benztropine (Cogentin®)
    Other medications that can cause drowsiness, such as zolpidem (Ambien®)
    How Long Does It Take For Hydroxyzine To Work?
    Symptoms of anxiety or insomnia may improve within hours of the first dose of medication.

    Summary Of FDA Black Box Warnings
    There are no FDA black box warnings for hydroxyzine.

  • Fanapt (Iloperidone)

    Brand name: Fanapt®

    Tablet: 1 mg, 2 mg, 4 mg, 6 mg, 8 mg, 10 mg, 12 mg
    Generic name: iloperidone (EYE loe PER i done)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Iloperidone And What Does It Treat?
    Iloperidone is a medication that works in the brain to treat schizophrenia. It is also known as a second generation antipsychotic (SGA) or atypical antipsychotic. Iloperidone rebalances dopamine and serotonin to improve thinking, mood, and behavior.

    Symptoms of schizophrenia include:

    Hallucinations — imagined voices or images that seem real
    Delusions — beliefs that are not true (e.g., other people are reading your thoughts)
    Disorganized thinking or trouble organizing your thoughts and making sense
    Little desire to be around other people
    Trouble speaking clearly
    Lack of motivation
    Iloperidone may help some or all of these symptoms.

    Iloperidone may also be helpful when prescribed "off-label" for other mental health conditions. "Off-label" means that it has not been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an "off-label" treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Iloperidone?
    Schizophrenia requires long-term treatment. Do not stop taking iloperidone, even when you feel better.

    With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of iloperidone may increase your risk for a relapse in your symptoms.

    Do not stop taking iloperidone or change your dose without talking with your healthcare provider first.

    For iloperidone to work properly, it should be taken every day as ordered by your healthcare provider.

    Are There Specific Concerns About Iloperidone And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with schizophrenia who wish to become pregnant face important decisions. This is a complex decision since untreated schizophrenia has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Antipsychotic use during the third trimester of pregnancy has a risk for abnormal muscle movements (extrapyramidal symptoms [EPS]) and/or withdrawal symptoms in newborns following delivery. Symptoms in the newborn may include agitation, feeding disorder, hypertonia, hypotonia, respiratory distress, somnolence, and tremor; these effects may be self-limiting or require hospitalization.

    Caution is advised with breastfeeding since there is currently no information available on whether iloperidone passes into human breast milk. In animal studies iloperidone was excreted in the milk of rats during lactation.

    What Should I Discuss With My Healthcare Provider Before Taking Iloperidone?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you ever had muscle stiffness, shaking, tardive dyskinesia, neuroleptic malignant syndrome, or weight gain caused by a medication
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any psychiatric or medical problems you have, such as heart rhythm problems, long QT syndrome, heart attacks, diabetes, high cholesterol, or seizures
    If you have a family history of diabetes or heart disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you smoke, drink alcohol, or use illegal drugs

    How Should I Take Iloperidone?
    Iloperidone is usually taken 2 times per day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 6 mg to 12 mg. Only your healthcare provider can determine the correct dose for you.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Iloperidone?
    If you miss a dose of iloperidone, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed. If you miss more than 3 days of medication, contact your prescriber because he/she may need to adjust your dose.

    What Should I Avoid While Taking Iloperidone?
    Avoid drinking alcohol or using illegal drugs while you are taking iloperidone. They may decrease the benefits (e.g. worsen your confusion) and increase adverse effects (e.g. sedation) of the medication.

    What Happens If I Overdose With Iloperidone?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of iloperidone does not exist.

    What Are Possible Side Effects Of Iloperidone?
    Common side effects

    Increased heart rate, dizziness, drowsiness, increased prolactin levels, weight gain

    Rare/serious side effects

    Iloperidone may increase the blood levels of a hormone called prolactin. Side effects of increased prolactin levels include females losing their period, production of breast milk and males losing their sex drive or possibly experiencing erectile problems. Long term (months or years) of elevated prolactin can lead to osteoporosis, or increased risk of bone fractures.

    Some people may develop muscle related side effects while taking iloperidone. The technical terms for these are “extrapyramidal symptoms” (EPS) and “tardive dyskinesia” (TD). Symptoms of EPS include restlessness, tremor, and stiffness. TD symptoms include slow or jerky movements that one cannot control, often starting in the mouth with tongue rolling or chewing movements.

    Temperature regulation: Impaired core body temperature regulation may occur; caution with strenuous exercise, heat exposure, and dehydration.

    Second generation antipsychotics (SGAs) increase the risk of weight gain, high blood sugar, and high cholesterol. This is also known as metabolic syndrome. Your healthcare provider may ask you for a blood sample to check your cholesterol, blood sugar, and hemoglobin A1c (a measure of blood sugar over time) while you take this medication.

    Information on healthy eating and adding exercise to decrease your chances of developing metabolic syndrome may be found at the following sites:

     

    http://www.helpguide.org/articles/healthy-eating/healthy-eating.htm
    http://www.helpguide.org/home-pages/exercise-fitness.htm
    SGAs have been linked with higher risk of death, strokes, and transient ischemic attacks (TIAs) in elderly people with behavior problems due to dementia.

    All antipsychotics have been associated with the risk of sudden cardiac death due to an arrhythmia (irregular heartbeat). To minimize this risk, antipsychotic medications should be used in the smallest effective dose when the benefits outweigh the risks. Your doctor may order an EKG to monitor for irregular heartbeat.

    Neuroleptic malignant syndrome is a rare, life threatening adverse effect of antipsychotics which occurs in

    All antipsychotics can cause sedation, dizziness, or orthostatic hypotension (a drop in blood pressure when standing up from sitting or lying down). These side effects may elad to falls which could cause bone fractures or other injuries. This risk is higher for people with conditions or other medications that could worsen these effects. If falls or any of these symptoms occur, contact your healthcare provider.

    Are There Any Risks For Taking Iloperidone For Long Periods Of Time?
    Tardive dyskinesia (TD) is a side effect that develops with prolonged use of antipsychotics. Medications such as iloperidone have been shown to have a lower risk of TD compared to older antipsychotics, such as Haldol (haloperidol). If you develop symptoms of TD, such as grimacing, sucking, and smacking of lips, or other movements that you cannot control, contact your healthcare provider immediately. All patients taking either first or second generation antipsychotics should have an Abnormal Involuntary Movement Scale (AIMS) completed regularly by their healthcare provider to monitor for TD.

    Second generation antipsychotics (SGAs) increase the risk of diabetes, weight gain, high cholesterol, and high triglycerides. (See “Serious Side Effects” section for monitoring recommendations.)

    What Other Medications May Interact With Iloperidone?
    Iloperidone may block the effects of agents used to treat Parkinson’s disease such as levodopa/carbidopa (Sinemet®), bromocriptine, pramipexole (Mirapex®), ropinirole (Requip®), and others.

    Iloperidone may lower your blood pressure. Medications used to lower blood pressure may increase this effect. Propranolol (Inderal®) is an example of this type of medication.

    The following medications may increase the risk of heart problems when used with iloperidone.

    Antipsychotics, including chlorpromazine (Thorazine®), thioridizine (Mellaril®), asenapine (Saphris®), paliperidone (Invega®), quetiapine (Seroquel®), and ziprasidone (Geodon®).
    Antiarrhythmics (heart rhythm medications), including procainamide, quinidine, amiodarone (Cordarone®), dronedarone (Multaq®), and sotalol (Betapace®)
    The following medications may increase the levels and effects of iloperidone: clarithromycin (Biaxin®), fluoxetine (Prozac®), ketoconazole (Nizoral®), and paroxetine (Paxil®).

    Carbamazepine (Tegretol®) may decrease the levels and effects of iloperidone.

    How Long Does It Take For Iloperidone To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking iloperidone. It will probably take several weeks to see big enough changes in your symptoms to decide if iloperidone is the right medication for you.

    Antipsychotic treatment is generally needed lifelong for persons with schizophrenia. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Hallucinations, disorganized thinking, and delusions may improve in the first 1-2 weeks
    Sometimes these symptoms do not completely go away
    Motivation and desire to be around other people can take at least 1-2 weeks to improve
    Symptoms continue to get better the longer you take iloperidone
    It may take 2-3 months before you get the full benefit of iloperidone


    Summary Of FDA Black Box Warnings
    Increased mortality in elderly patients with dementia-related psychosis

    Both first generation (typical) and second generation (atypical) antipsychotics are associated with an increased risk of mortality in elderly patients when used for dementia related psychosis.
    Although there were multiple causes of death in studies, most deaths appeared to be due to cardiovascular causes (e.g. sudden cardiac death) or infection (e.g. pneumonia).
    Antipsychotics are not indicated for the treatment of dementia-related psychosis.

  • Lamictal (Lamotrigine)

    Brand name:

    Lamictal®Tablet: 25 mg, 100 mg, 150 mg, 200 mg
    Chewable tablet: 2 mg, 5 mg, 25 mg
    Oral Disintegrating tablet: 25 mg, 50 mg, 100 mg, 200 mg
    Two different dosing "starter" kits are also available. One is for patients who are already taking valproate (Depakote®); the other is for patients who are already taking carbamazepine (Tegretol®).
    Lamictal® XRTablet (extended release): 25mg, 50 mg, 100 mg, 200 mg
    Generic name: lamotrigine (la MOE tri jeen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Lamotrigine And What Does It Treat?
    Lamotrigine is a mood stabilizer medication that works in the brain. It is approved for the treatment of bipolar disorder (also known as manic depression) and certain types of seizure disorders. Bipolar disorder involves episodes of depression and/or mania.

    Symptoms of depression include:

    Depressed mood – feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, or helpless
    Loss of interest or pleasure in normal activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving in slow motion)
    Symptoms of mania include:Feeling irritable or “high”
    Having increased self esteem
    Feeling like you don’t need to sleep
    Feeling the need to continue to talk
    Feeling like your thoughts are too quick (racing thoughts)
    Feeling distracted
    Getting involved in activities that are risky or could have bad consequences (e.g., excessive spending)
    Lamotrigine may also be helpful when prescribed “off-label” for bipolar depression. “Off-label” means that it hasn’t been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an “off-label” treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Lamotrigine?
    Bipolar disorder requires long-term treatment. Do not stop taking lamotrigine, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine. Missing doses of lamotrigine may increase your risk for a relapse in your mood symptoms.

    Do not stop taking lamotrigine or change your dose without talking to your health care provider first.

    In order for lamotrigine to work properly, it should be taken every day as ordered by your health care provider.

    Are There Specific Concerns About Lamotrigine And Pregnancy?
    If you are planning on becoming pregnant, notify your health care provider so that he/she can best manage your medications. People living with bipolar disorder who wish to become pregnant face important decisions. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Lamotrigine has been associated with an increased risk of oral cleft birth defects. There may be precautions to decrease the risk of this effect. Do not stop taking lamotrigine without first speaking to your health care provider. Discontinuing similar medications during pregnancy has been associated with a significant increase in symptom relapse.

    Regarding breastfeeding, caution is advised since lamotrigine does pass into breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Lamotrigine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you drink alcohol or use illegal drugs
    How Should I Take Lamotrigine?
    Lamotrigine is usually taken 1 or 2 times daily with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 25 mg to 400 mg. Only your health care provider can determine the correct dose for you.

    Extended release tablets: Swallow whole. Do not crush, chew or split tablets.

    Lamotrigine orally disintegrating tablets must remain in their original packaging. Open the package with clean dry hands before each dose. Do not try to put tablets in a pillbox if you take the orally disintegrating tablets. Lamotrigine orally disintegrating tablets will dissolve in your mouth within seconds and can be swallowed with or without liquid.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Lamotrigine?
    If you miss a dose of lamotrigine, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your health care provider. Do not double your dose or take more than what is prescribed. If you miss more than 3 days of medication, contact your prescriber because he/she may need to adjust your dose.

    What Should I Avoid While Taking Lamotrigine?
    Avoid drinking alcohol or using illegal drugs while you are taking lamotrigine. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Lamotrigine?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of lamotrigine does not exist.

    What Are Possible Side Effects Of Lamotrigine?
    Common side effects

    Nausea
    Insomnia
    Runny nose
    Non-serious rash
    Headache
    Diarrhea
    Abnormal dreams
    Dizziness or drowsiness
    Fatigue


    Rare/serious side effects

    A serious, life-threatening skin rash (also known as Stevens–Johnson Syndrome) may occur with the use of lamotrigine. Contact your health care provider immediately if you have any of the following: a skin rash, blistering or peeling of your skin, hives, shortness of breath, or painful sores in your mouth or around your eyes. Extra caution is needed in children and teenagers ages 2-17 receiving lamotrigine. These patients may be at an increased risk of developing this life-threatening rash.

    Studies have found that individuals who take antiepileptic medications including lamotrigine have suicidal thoughts or behaviors up to twice as often than individuals who take placebo (inactive medication). These thoughts or behaviors occurred in approximately 1 in 500 patients taking the antiepileptic class of medications. If you experience any thoughts or impulses to hurt yourself, you should contact your doctor immediately.

    Aseptic meningitis, a serious inflammation of the protective membrane that covers the brain and spinal cord has been identified as a very rare but serious side effect of lamotrigine. Contact your health care provider immediately if you experience headache, fever, nausea, vomiting, stiff neck, rash, unusual sensitivity to light, muscle pains, chills, confusion, or drowsiness while taking lamotrigine.

    A rare but life-threatening immune system reaction which can cause serious blood or liver problems has been reported with lamotrigine use. Contact your health care provider immediately if you experience fever, frequent infections, severe muscle pain, swelling of the face, eyes, lips, or tongue, swollen lymph glands, unusual bruising or bleeding, weakness, fatigue, or yellowing of the skin or white part of your eyes. Onset usually occurs within the first several weeks after starting therapy. Patients with hemophagocytic lymphohistiocytosis (HLH) symptoms should be evaluated promptly; discontinuation and conversion to alternate therapy may be required.

    Seizures may occur if a patient taking lamotrigine suddenly stops taking it.

    A rare but serious multiorgan hypersensitivity reactions, also known as drug reaction with eosinophilia and systemic symptoms (DRESS), which may damage organs, including the liver, kidney, or heart have been reported with the use of lamotrigine. Contact your health care provider immediately if you experience fever, rash, swollen or enlarged lymph nodes. Discontinuation and conversion to alternate therapy may be required.

    Are There Any Risks For Taking Lamotrigine For Long Periods Of Time?
    To date, there are no known problems associated with long term use of lamotrigine. It is a safe and effective medication when used as directed.

    It is important to note that some of the side effects listed above (particularly rash and suicidal thoughts) may continue to occur or worsen if you continue taking the medication. It is important to follow up with your doctor routinely and to contact your doctor immediately if you notice any skin rash or changes in mood or behavior.

    What Other Medications May Interact With Lamotrigine?
    The following medications may increase the level and effects of lamotrigine:

    Valproate/divalproex (Depakote®)
    The following medications may decrease the level and effect of lamotrigine:

    Anticonvulsants such as phenytoin (Dilantin®), carbamazepine (Tegretol®/Carbatrol®/Equetro®), phenobarbital, and primidone (Mysoline®)
    Oral contraceptives (birth control pills)
    Rifampin (Rifadin®), ritonavir (Norvir®)
    Lamotrigine may increase the level and effects of: Clozapine (Clozaril®, FazaClo®)


    How Long Does It Take For Lamotrigine To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking lamotrigine. It will probably take several weeks to see big enough changes in your symptoms to decide if lamotrigine is the right medication for you.

    Mood stabilizer treatment is generally needed lifelong for persons with bipolar disorder. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Summary Of FDA Black Box Warnings
    Serious skin reactions

    Serious and sometimes fatal skin reactions have been reported with lamotrigine use. Since it is not always possible to predict which rashes will prove to be serious or life threatening, it is important to talk to your doctor at the first sign of a rash while taking lamotrigine.

  • Fetzima (Levomilnacipran)

    Brand name: Fetzima®

    Capsules (extended release): 20 mg, 40 mg, 80 mg, 120 mg

    Generic name: levomilnacipran (lee voe mil NA si pran)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Levomilnacipran And What Does It Treat?
    Levomilnacipran is an antidepressant medication that works in the brain. It is approved for the treatment of major depressive disorder (MDD).

    Symptoms of depression include:

    Depressed mood - feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, and helpless
    Loss of interest or pleasure in your usual activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving and thinking in slow motion)
    Suicidal thoughts or behaviors

    What Is The Most Important Information I Should Know About Levomilnacipran?
    Do not stop taking levomilnacipran, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of levomilnacipran may increase your risk for relapse in your symptoms.

    Stopping levomilnacipran abruptly may result in one or more of the following withdrawal symptoms: irritability, nausea, dizziness, vomiting, nightmares, headache, and/or paresthesias (prickling, tingling sensation on the skin).

    Depression is also a part of bipolar illness. People with bipolar disorder who take antidepressants may be at risk for "switching" from depression into mania. Symptoms of mania include "high" or irritable mood, very high self-esteem, decreased need for sleep, pressure to keep talking, racing thoughts, being easily distracted, frequently involved in activities with a large risk for bad consequences (for example, excessive buying sprees).

    Medical attention should be sought if serotonin syndrome is suspected. Please refer to serious side effects for signs/symptoms.

    Are There Specific Concerns About Levomilnacipran And Pregnancy?
    If you are planning on becoming pregnant, notify your health care provider to best manage your medications. People living with MDD who wish to become pregnant face important decisions. Untreated MDD has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers. For women who take antidepressant medications during weeks 13 through the end of their pregnancy (second and third trimesters), there is a risk that the baby can be born before it is fully developed (before 37 weeks).

    Regarding breastfeeding, caution is advised since it is not known if levomilnacipran passes into breast milk, so it is important to discuss this with your doctor and caregivers.

    What Should I Discuss With My Health Care Provider Before Taking Levomilnacipran?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, including a history of bipolar disorder
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breastfeeding
    If you drink alcohol or use drugs

    How Should I Take Levomilnacipran?
    Levomilnacipran is usually taken one time per day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased after a few days.

    The dose usually ranges from 20 mg to 120 mg. Only your health care provider can determine the correct dose for you.

    Take the capsules whole; do not open, crush, or chew.

    Consider using a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Levomilnacipran?
    If you miss a dose of levomilnacipran, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your health care provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Levomilnacipran?
    Avoid drinking alcohol or using illegal drugs while you are taking antidepressant medications. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Levomilnacipran?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of levomilnacipran does not exist.

    What Are The Possible Side Effects Of Levomilnacipran?
    Common side effects

    Nausea, vomiting, orthostatic hypotension, constipation, increased sweating, increased heart rate, palpitations, difficulty urinating, decreased appetite. These will often improve over the first week or two as you continue to take the medication.

    Sexual side effects, such as problems with orgasm or ejaculatory delay, often do not diminish over time.

    Rare/serious side effects

    Serotonin syndrome (symptoms may include shivering, diarrhea, confusion, severe muscle tightness, fever, seizures, and death), increased blood pressure, low sodium (symptoms of low sodium levels may include headache, weakness, difficulty concentrating and remembering), angle closure glaucoma (symptoms of angle closure glaucoma may include eye pain, changes in vision, swelling or redness in or around eye)

    Levomilnacipran may increase the risk of bleeding events. Combined use of aspirin, nonsteroidal anti-inflammatory drugs (e.g., ibuprofen, naproxen), warfarin, and other anti-coagulants may increase this risk. This may include gums that bleed more easily, nose bleed, or gastrointestinal bleeding. Some cases have been life threatening.

    Are There Any Risks For Taking Levomilnacipran For Long Periods Of Time?
    To date, there are no known problems associated with long term use of levomilnacipran. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Levomilnacipran?
    Levomilnacipran should not be taken with or within 2 weeks of taking monoamine oxidase inhibitors (MAOIs). These include phenelzine (Nardil®), tranylcypromine (Parnate®), isocarboxazid (Marplan®), and selegiline (Emsam®).

    Although rare, there is an increased risk of serotonin syndrome when levomilnacipran is used with other medications that increase serotonin, such as other antidepressants, migraine medications called “triptans” (e.g., Imitrex®), some pain medications (e.g., tramadol (Ultram®)), and the antibiotic linezolid (Zyvox®).

    Levomilnacipran may increase the effects of other medications that can cause bleeding (e.g., ibuprofen (Advil®, Motrin®), warfarin (Coumadin®), and aspirin).

    The following medications may increase the levels and effects of levomilnacipran:

    The following medications may increase the levels and effects of levomilnacipran:
    Antibiotics, such as clarithromycin (Biaxin®) and azithromycin (Zithromax®)
    Antidepressants, such as fluoxetine (Prozac®), paroxetine (Paxil®), and nefazodone
    Antifungals, such as fluconazole (Diflucan®), ketoconazole (Nizoral®), and itraconazole (Sporanox®)
    The antiarrhymia agent quinidine
    HIV medications, such as the protease inhibitors indinavir (Crixivan®), ritonavir (Norvir®), saquinavir (Fortovase®, Invirase®), and lopinavir/ritonavir (Kaletra®)

    How Long Does It Take For Levomilnacipran To Work?
    Sleep, energy, or appetite may show some improvement within the first 1-2 weeks. Improvement in these physical symptoms can be an important early signal that the medication is working. Depressed mood and lack of interest in activities may need up to 6-8 weeks to fully improve.

    Summary Of FDA Black Box Warnings
    Suicidal thoughts or actions in children and adults

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide. Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking antidepressant medications. This risk may persist until significant remission occurs.

    In short-term studies, antidepressants increased the risk of suicidality in children, adolescents, and young adults when compared to placebo. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24. Adults age 65 and older taking antidepressants have a decreased risk of suicidality. Patients, their families, and caregivers should be alert to the emergence of anxiety, restlessness, irritability, aggressiveness and insomnia. If these symptoms emerge, they should be reported to the patient’s prescriber or health care professional. All patients being treated with antidepressants for any indication should watch for and notify their health care provider for worsening symptoms, suicidality and unusual changes in behavior, especially during the first few months of treatment.

     

  • Lithium

    Brand names:

    Eskalith®Immediate release tablets: 300mg
    Immediate release capsules: 150 mg, 300 mg, 600 mg
    Oral solution (liquid): 8 mEq/5 mL
    Eskalith CR®, Lithobid®Tablets (extended release): 300 mg, 450 mg
    Generic name: lithium (LITH ee um)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Lithium And What Does It Treat?
    Lithium is a mood stabilizer medication that works in the brain. It is approved for the treatment of bipolar disorder (also known as manic depression). Bipolar disorder involves episodes of depression and/or mania.

    Symptoms of depression include:

    Depressed mood — feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, or helpless
    Loss of interest or pleasure in normal activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving in slow motion)
    Symptoms of mania include:

    Feeling irritable or “high”
    Having increased self esteem
    Feeling like you don’t need to sleep
    Feeling the need to continue to talk
    Feeling like your thoughts are too quick (racing thoughts)
    Feeling distracted
    Getting involved in activities that are risky or could have bad consequences (e.g., excessive spending)
    Lithium may also be helpful when prescribed “off-label” for depression, especially when combined with antidepressant medications. “Off-label” means that it hasn’t been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an “off-label” treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Lithium?
    Bipolar disorder requires long-term treatment. Do not stop taking lithium, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine. Missing doses of lithium may increase your risk for a relapse in your mood symptoms.

    Do not stop taking lithium or change your dose without talking to with your healthcare provider first.

    In order for lithium to work properly, it should be taken every day as ordered by your healthcare provider.

    Periodically, your healthcare provider may ask you to provide a blood sample to make sure the appropriate level of medication is in your body and to assess for side effects, such as changes in blood cell counts or kidney function.

    Are There Specific Concerns About Lithium And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider so that he/she can best manage your medications. People living with bipolar disorder who wish to become pregnant face important decisions. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Lithium has been associated with an increased risk of Ebstein’s anomaly, a heart valve defect. Even though data suggest that the risk of Ebstein’s anomaly from first trimester use of lithium is very low, an ultrasound of the heart is recommended at 16 to 20 weeks of gestation. Lithium levels should be monitored monthly in early pregnancy and weekly near delivery. Do not stop taking lithium without first speaking to your healthcare provider. Discontinuing mood stabilizer medications during pregnancy has been associated with a significant increase in symptom relapse.

    Regarding breast-feeding, caution is advised since lithium does pass into breast milk. In general, breastfeeding is not recommended while taking lithium.

    What Should I Discuss With My Healthcare Provider Before Taking Lithium?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you drink alcohol or use illegal drugs
    How Should I Take Lithium?
    Lithium is usually taken 1-3 times per day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 600 mg to 1200 mg daily, but some people may require higher doses depending on weight or symptoms. Only your healthcare provider can determine the correct dose for you.

    Extended release tablets: Swallow the tablet whole. Do not crush or chew extended release tablets.

    Liquid: Measure with a dosing spoon or oral syringe, which you can get from your pharmacy.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Lithium?
    If you miss a dose of lithium, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your dose or take more than what is prescribed.

    What Should I Avoid While Taking Lithium?
    Avoid drinking alcohol or using illegal drugs while you are taking lithium. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    Avoid low sodium diets and dehydration because this can increase the risk of lithium toxicity.

    Avoid over the counter and prescription pain medications that contain nonsteroidal anti-inflammatory medications (NSAIDS) such as ibuprofen (Motrin®, Advil®) or naproxen (Aleve®, Naprosyn®) because these medications can increase the risk of toxicity from lithium.

    Avoid excessive intake of caffeinated beverages, such as coffee, tea, cola or energy drinks, since these may decrease levels of lithium and decrease effectiveness of the medication. Discontinuing caffeine use may increase lithium levels. Consult your healthcare provider before reducing or stopping caffeine use.

    What Happens If I Overdose With Lithium?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of lithium does not exist, but there are treatments to decrease the effects of the medication. Only a doctor can determine if you require treatment.

    What Are Possible Side Effects Of Lithium?
    Common side effects

    Headache
    Nausea or vomiting
    Diarrhea
    Dizziness or drowsiness
    Changes in appetite
    Hand tremors
    Dry mouth
    Increased thirst
    Increased urination
    Thinning of hair or hair loss
    Acne-like rash


    Rare/serious side effects

    Signs of lithium toxicity include severe nausea and vomiting, severe hand tremors, confusion, vision changes, and unsteadiness while standing or walking. These symptoms need to be addressed immediately with a medical doctor to ensure your lithium level is not dangerously high.

    In rare cases, lithium may lead to a reversible condition known as diabetes insipidus. If this occurs you would notice a significant increase in thirst and how much fluid you drink and how much you urinate. Talk to your doctor if you notice you are urinating more frequently than usual.

    Are There Any Risks For Taking Lithium For Long Periods Of Time?
    Hypothyroidism (low levels of thyroid hormone) may occur with long-term lithium use.

    Rare kidney problems have been associated with long-term use of lithium. The risk increases with high levels of lithium. Your doctor will monitor your kidney function at routine check-ups to ensure this does not occur.

    What Other Medications May Interact With Lithium?
    The following medications can increase the levels and effects of lithium:

    Diuretics, such as: hydrochlorothiazide (Microzide®), furosemide (Lasix®), bumetanide (Bumex®), torsemide (Demadex®), acetazolamide (Diamox®), chlorthiazide (Diuril®), and chlorthalidone (Thalitone®)
    Non-steroidal anti-inflammatory medications (NSAIDs) including: Ibuprofen (Advil®, Motrin®), naproxen (Naprosyn®), celecoxib (Celebrex®), diclofenac (Voltaren®), and nabumetone (Relafen®)
    Certain blood pressure medications, called angiotensin receptor blockers or angiotensin converting enzyme inhibitors.Angiotensin receptor blockers (ARBs): valsartan (Diovan®), olmesartan (Benicar®), candesartan (Atacand®), losartan (Cozaar®)
    Angiotensin converting enzyme (ACE) inhibitors: enalapril (Vasotec®), captopril (Capoten®), benazepril (Lotensin®), fosinopril (Monopril®)
    Certain antidepressants, known as monoamine oxidase inhibitors (MAOIs). Examples include phenelzine (Nardil®), tranylcypromine (Parnate®), selegiline (Eldepryl®, Emsam®), and isocarboxazid (Marplan®)
    The following medications may decrease the levels and effect of lithium:

    Caffeine
    Sodium chloride (table salt)
    A medication used to treat breathing problems called theophylline (Theo–Dur®, Slo–Bid®)

    How Long Does It Take For Lithium To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking lithium. It will probably take several weeks to see big enough changes in your symptoms to decide if lithium is the right medication for you.

    Mood stabilizer treatment is generally needed lifelong for persons with bipolar disorder. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Summary Of Black Box Warnings
    Lithium toxicity

    Lithium toxicity is closely related to lithium blood levels and can occur at doses close to therapeutic levels; lithium levels should be monitored closely when starting the medication or if individuals experience side effects of the medication.

  • Lucemyra (Lofexidine)

    Brand name: Lucemyra®

    Tablet: 0.18 mg
    Generic name: lofexidine (loe FEX i deen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Lofexidine And What Does It Treat?
    Lofexidine is a non-opioid prescription medicine used in adults to help with the symptoms of opioid withdrawal that may happen when you stop taking an opioid suddenly. Lofexidine will not completely prevent the symptoms of opioid withdrawal.

    Symptoms of opioid withdrawal include:

    Aches and pains
    Stomache cramps
    Feeling sick
    Muscle spasms/twitching
    Insomnia/problems sleeping
    Feeling of coldness/chills
    Muscular tension
    Heart pounding
    Runny eyes
    Yawning

    What Is The Most Important Information I Should Know About Lofexidine?
    Lofexidine is not a treatment for opioid use disorder. If you have been diagnosed with opioid use disorder, your healthcare provider may prescribe lofexidine as part of a complete treatment program for your opioid use disorder.

    Lofexidine may cause low blood pressure, slow heart rate, and fainting. Notify your healthcare provider right away if you experience these symptoms. If you take lofexidine and have any of these symptoms, do not take your next dose until you have talked to your healthcare provider. You should stay well-hydrated and avoid becoming overheated during treatment with lofexidine because that can increase your risk of low blood pressure and fainting. You should also be careful to stand up slowly from lying down or sitting.

    After the period of time of not using opioid medications, you will respond to lower doses of opioids for pain. Do not begin using opioids at the doses you tolerated prior to starting lofexidine. This may increase your risk of overdose and death.

    Lofexidine can potentiate the central nervous system depressant effects of benzodiazepines, alcohol, barbiturates, and other sedating drugs.

    Lofexidine should be used in conjunction with a comprehensive treatment program. Lofexidine treatment should be discontinued by slowly decreasing the dose.

    Are There Specific Concerns About Lofexidine And Pregnancy?
    There is limited data on lofexidine use in pregnant women to inform about drug-associated risk. The safety of lofexidine in pregnant women has not been established.

    There is no information regarding the presence of lofexidine or its metabolites in human milk, the effects on the breastfed infant, or the effects on milk production. Caution should be exercised when lofexidine is administered to a nursing woman.

    Your healthcare provider and you should consider your clinical need for lofexidine and any other potential adverse effects on breastfed children from lofexidine or from the underlying maternal condition.

    What Should I Discuss With My Health Care Provider Before Taking Lofexidine?
    If you have low blood pressure
    If you have a slow heart rate
    If you have any heart problems, including history of heart attack or a condition called long QT syndrome
    If you have liver or kidney problems
    If you drink alcohol
    If you are pregnant or plan to become pregnant. It is not known if lofexidine can harm your unborn baby.
    If you are breastfeeding or plan to breastfeed. It is not known if lofexidine passes into your breast milk. Talk to your healthcare provider about the best way to feed your baby during treatment with lofexidine.
    Tell your healthcare provider about all of the medicines you take, including prescription and over-the-counter medicines, vitamins, herbal supplements, and any medications you may take for the individual symptoms of opioid withdrawal (such as pain relievers or medications for upset stomach).
    Tell your healthcare provider if you take benzodiazepines, barbiturates, tranquilizers, or sleeping pills. Taking lofexidine with these medicines can cause serious side effects. Ask your healthcare provider or pharmacist if you are not sure if you are taking any of these medicines.

    How Should I Take Lofexidine?
    Lofexidine should be taken exactly as your healthcare provider tells you to take it. Do not change your dose or stop taking lofexidine without talking to your healthcare provider.

    Take lofexidine with or without food. You should wait at least 5 to 6 hours between each dose. You should drink plenty of non-caffeine liquids, unless told otherwise by your doctor. You should never take more than 16 tablets in 1 day and no single dose should exceed 4 tablets.

    Consider using a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Lofexidine?
    If you miss a dose of lofexidine, take it as soon as you remember unless it is closer to the time of your next dose. Do not double your next dose or take more than what is prescribed. You should wait at least 5 to 6 hours between each dose.

    What Should I Avoid While Taking Lofexidine?
    Do not drive, operate heavy machinery, or perform any other dangerous activities until you know how lofexidine affects you. Avoid drinking alcohol, using opioid pain medications (such as codeine, hydrocodone, oxycodone, or morphine), or using illegal drugs while you are taking lofexidine. They may increase adverse effects (e.g., sedation) of the medication.

    Keep in mind that some cough syrups may contain opioid pain medication. Discuss all medications with your doctor and pharmacist prior to taking lofexidine.

    What Happens If I Overdose With Lofexidine?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    Signs and symptoms of an overdose include:

    Low blood pressure
    Slow heart rate
    Sedation

    What Are The Possible Side Effects Of Lofexidine?
    Common side effects

    Low blood pressure or symptoms of low blood pressure (e.g., lightheadedness)
    Slow heart rate
    Dizziness
    Sleepiness
    Dry mouth

    Rare/serious side effects

    Irregular heart rhythms: Notify your healthcare provider if you have a history of congestive heart failure, slow heart rate, liver or kidney problems.
    Opioid overdose: If you complete opioid discontinuation, you are likely to have a reduced tolerance to opioids and are at an increased risk of a fatal overdose if resume opioid use.
    Discontinuation syndrome: Marked rise in blood pressure and symptoms of diarrhea, insomnia, anxiety, chills, sweating and extremity pain. Lofexidine must be discontinued gradually.

    Are There Any Risks For Taking Lofexidine For Long Periods Of Time?
    Lofexidine is not indicated for long-term use. Lofexidine treatment usually last for 5 to 7 days following last opioid use. It may only be continued up to 14 days with dosing guided by symptoms. Lofexidine must be discontinued gradually over a 2 to 4-day period.

    What Other Medications May Interact With Lofexidine?
    Lofexidine may increase the depressant effects of benzodiazepines, barbiturates and other sedating drugs.

    Paroxetine (Paxil®) may increase the absorption of lofexidine, which can increase the side effects of lofexidine (e.g., low blood pressure, slow heart rate). Lofexidine may reduce the effectiveness of oral naltrexone (Revia®) when given within 2 hours of each other. Taking lofexidine and methadone together may cause irregular heart rhythms. Concurrent use requires cardiac monitoring.

    Your pharmacist or doctor will help you to determine if other medications you take can interfere with the effects of lofexidine.

    How Long Does It Take For Lofexidine To Work?
    Lofexidine will begin working shortly after taking one dose.

    Summary Of FDA Black Box Warnings
    There are no FDA black box warnings for lofexidine.

  • Loxitane (Loxapine)

    Brand names: Loxitane®, Adasuve®

    Loxitane® Capsule: 5mg, 10mg, 25mg, 50mg
    Adasuve® Aerosol powder: 10mg
    Generic name: loxapine (LOKS a peen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Loxapine And What Does It Treat?
    Loxapine is a medication that works in the brain to treat schizophrenia. It is also known as a first generation antipsychotic (FGA) or typical antipsychotic. Loxapine rebalances dopamine to improve thinking, mood, and behavior.

    Symptoms of schizophrenia include:

    Hallucinations — imagined voices or images that seem real
    Delusions — beliefs that are not true (e.g., other people are reading your thoughts)
    Disorganized thinking or trouble organizing your thoughts and making sense
    Little desire to be around other people
    Trouble speaking clearly
    Lack of motivation
    Loxapine may help some or all of these symptoms.

    Loxapine powder for inhalation (Adasuve®) is FDA approved for the treatment of acute agitation associated with schizophrenia or bipolar disorder in adults.

    Loxapine may also be helpful when prescribed "off-label" for other mental health conditions. "Off-label" means that it has not been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an "off-label" treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Loxapine?
    Schizophrenia requires long-term treatment. Do not stop taking loxapine, even when you feel better.

    With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of loxapine may increase your risk for a relapse in your symptoms.

    Do not stop taking loxapine or change your dose without talking to with your healthcare provider first.

    For loxapine to work properly, it should be taken every day as ordered by your healthcare provider.

    Are There Specific Concerns About Loxapine And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with schizophrenia who wish to become pregnant face important decisions. This is a complex decision since untreated schizophrenia has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Antipsychotic use during the third trimester of pregnancy has a risk for abnormal muscle movements (extrapyramidal symptoms [EPS]) and/or withdrawal symptoms in newborns following delivery. Symptoms in the newborn may include agitation, feeding disorder, hypertonia, hypotonia, respiratory distress, somnolence, and tremor; these effects may be self-limiting or require hospitalization.

    Caution is advised with breast-feeding since it is not known whether loxapine is excreted in breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Loxapine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you ever had muscle stiffness, shaking, tardive dyskinesia, neuroleptic malignant syndrome, or weight gain caused by a medication
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any psychiatric or medical problems you have, such as heart rhythm problems, long QT syndrome, heart attacks, diabetes, high cholesterol, or seizures
    If you have a family history of diabetes or heart disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you smoke, drink alcohol, or use illegal drugs
    How Should I Take Loxapine?
    Loxapine is usually taken twice a day.

    Typically, patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 10mg to 250mg daily. Only your healthcare provider can determine the correct dose for you.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication.  You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    The inhalation form is used once daily.

    What Happens If I Miss A Dose Of Loxapine?
    If you miss a dose of loxapine, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Loxapine?
    Avoid drinking alcohol or using illegal drugs while you are taking loxapine. They may decrease the benefits (e.g. worsen your confusion) and increase adverse effects (e.g. sedation) of the medication.

    What Happens If I Overdose With Loxapine?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of loxapine does not exist.

    What Are Possible Side Effects Of Loxapine?
    Common side effects

    Oral: Low blood pressure, fainting, sleepiness

    Powder for inhalation: Distortion in sense of taste, respiratory distress

    Rare side effects

    Loxapine may increase the blood levels of a hormone called prolactin. Side effects of increased prolactin levels include females losing their period, production of breast milk and males losing their sex drive or possibly experiencing erectile problems. Long term (months or years) of elevated prolactin can lead to osteoporosis or increased risk of bone fractures.

    Serious side effects

    Some people may develop muscle related side effects while taking loxapine. The technical terms for these are “extrapyramidal symptoms” (EPS) and “tardive dyskinesia” (TD). Symptoms of EPS include restlessness, tremor, and stiffness. TD symptoms include slow or jerky movements that one cannot control, often starting in the mouth with tongue rolling or chewing movements.

    All antipsychotics have been associated with the risk of sudden cardiac death due to an arrhythmia (irregular heartbeat). To minimize this risk, antipsychotic medications should be used in the smallest effective dose when the benefits outweigh the risks. Your doctor may order an EKG to monitor for irregular heartbeat.

    Neuroleptic malignant syndrome is a rare, life threatening adverse effect of antipsychotics which occurs in

    All antipsychotics can cause sedation, dizziness, or orthostatic hypotension (a drop in blood pressure when standing up from sitting or lying down). These side effects may lead to falls which could cause bone fractures or other injuries. This risk is higher for people with conditions or other medications that could worsen these effects. If falls or any of these symptoms occur, contact your healthcare provider.

    Are There Any Risks For Taking Loxapine For Long Periods Of Time?
    Tardive dyskinesia (TD) is a side effect that develops with prolonged use of antipsychotics. If you develop symptoms of TD, such as grimacing, sucking, and smacking of lips, or other movements that you cannot control, contact your healthcare provider immediately. All patients taking either first or second generation antipsychotics should have an Abnormal Involuntary Movement Scale (AIMS) completed regularly by their healthcare provider to monitor for TD.

    What Other Medications May Interact With Loxapine?
    Other medications taken into the lungs may interfere with the effectiveness of the Adasuve aerosol formulation of loxapine. You should check with your doctor if you also use any type of inhaler for asthma or COPD.

    How Long Does It Take For Loxapine To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking loxapine. It will probably take several weeks to see big enough changes in your symptoms to decide if loxapine is the right medication for you.

    Antipsychotic treatment is generally needed lifelong for persons with schizophrenia. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Hallucinations, disorganized thinking, and delusions may improve in the first 1-2 weeks
    Sometimes these symptoms do not completely go away
    Motivation and desire to be around other people can take at least 1-2 weeks to improve
    Symptoms continue to get better the longer you take loxapine.
    It may take 2-3 months before you get the full benefit of loxapine.


    Summary Of FDA Black Box Warnings
    Increased mortality in elderly patients with dementia-related psychosis

    Both first generation (typical) and second generation (atypical) antipsychotics are associated with an increased risk of mortality in elderly patients when used for dementia related psychosis.
    Although there were multiple causes of death in studies, most deaths appeared to be due to cardiovascular causes (e.g. sudden cardiac death) or infection (e.g. pneumonia).
    Antipsychotics are not indicated for the treatment of dementia-related psychosis.
    Bronchospasm (Powder for inhalation)

    Inhaled loxapine can cause bronchospasm which is a spasm or contraction of the airway. This can lead to severe difficulty breathing or inability to continue breathing.
    Inhaled loxapine should only be administered in a registered enrolled healthcare facility with immediate access to on-site equipment and personnel trained to manage acute bronchospasm including advanced airway management (intubation and mechanical ventilation).
    Before using loxapine inhalation, prescribers should screen patients for a history of asthma, COPD, other lung diseases that may cause bronchospasm, or acute respiratory symptoms. Patients should also be screened for current use of medications used to treat airway disease.
    Loxapine can cause sedation, which may mask the signs of bronchospasm.

  • Latuda (Lurasidone)

    Brand name: Latuda®​

    Tablet: 20 mg, 40 mg, 60 mg, 80 mg, 120 mg
    Generic name: Lurasidone (loo RAS I done)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Lurasidone And What Does It Treat?
    Lurasidone is a medication that works in the brain to treat schizophrenia. It is also known as a second generation antipsychotic (SGA) or atypical antipsychotic. Lurasidone rebalances dopamine and serotonin to improve thinking, mood, and behavior.

    Symptoms of schizophrenia include:

    Hallucinations — imagined voices or images that seem real
    Delusions — beliefs that are not true (e.g., other people are reading your thoughts)
    Disorganized thinking or trouble organizing your thoughts and making sense
    Little desire to be around other people
    Trouble speaking clearly
    Lack of motivation
    Lurasidone may help some or all of these symptoms.

    Lurasidone is also FDA approved for the treatment of depressive phases of bipolar disorder.

    This medication sheet will focus primarily on schizophrenia. You can find more information about bipolar disorder here.

    Lurasidone may also be helpful when prescribed “off-label” for major depressive disorder psychosis or agitation associated with dementia. “Off-label” means that it has not been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an “off-label” treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Lurasidone?
    Schizophrenia requires long-term treatment. Do not stop taking lurasidone, even when you feel better.

    With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of lurasidone may increase your risk for a relapse in your symptoms.

    Do not stop taking lurasidone or change your dose without talking with your healthcare provider first.

    For lurasidone to work properly, it should be taken every day as ordered by your healthcare provider.

    Are There Specific Concerns About Lurasidone And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with schizophrenia who wish to become pregnant face important decisions. This is a complex decision since untreated schizophrenia has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Antipsychotic use during the third trimester of pregnancy has a risk for abnormal muscle movements (extrapyramidal symptoms [EPS]) and/or withdrawal symptoms in newborns following delivery. Symptoms in the newborn may include agitation, feeding disorder, hypertonia, hypotonia, respiratory distress, somnolence, and tremor; these effects may be self-limiting or require hospitalization.

    Caution is advised with breastfeeding since it is not known if lurasidone passes into breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Lurasidone?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you ever had muscle stiffness, shaking, tardive dyskinesia, neuroleptic malignant syndrome, or weight gain caused by a medication
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any psychiatric or medical problems you have, such as heart rhythm problems, long QT syndrome, heart attacks, diabetes, high cholesterol, or seizures
    If you have a family history of diabetes or heart disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you smoke, drink alcohol, or use illegal drugs
    How Should I Take Lurasidone?
    Lurasidone is usually taken 1 time per day with food (at least 350 calories).

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    For schizophrenia, the dose usually ranges from 40 mg to 160 mg. Only your healthcare provider can determine the correct dose for you.

    For acute treatment of depressive episodes of bipolar disorder (when used alone or with lithium or valproate), the dose usually ranges from 20 mg to 120 mg. Only your healthcare provider can determine the correct dose for you.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Lurasidone?
    If you miss a dose of lurasidone, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Lurasidone?
    Avoid drinking alcohol or using illegal drugs while you are taking lurasidone. They may decrease the benefits (e.g. worsen your confusion) and increase adverse effects (e.g. sedation) of the medication.

    What Happens If I Overdose With Lurasidone?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of lurasidone does not exist.

    What Are Possible Side Effects Of Lurasidone?
    Common side effects

    Extrapyramidal symptoms, drowsiness, restlessness, insomnia, increased glucose, cholesterol abnormalities, nausea, viral infection

    Rare/serious side effects

    Lurasidone may increase the blood levels of a hormone called prolactin. Side effects of increased prolactin levels include females losing their period, production of breast milk and males losing their sex drive or possibly experiencing erectile problems. Long term (months or years) of elevated prolactin can lead to osteoporosis, or increased risk of bone fractures.

    Some people may develop muscle related side effects while taking lurasidone. The technical terms for these are “extrapyramidal symptoms” (EPS) and “tardive dyskinesia” (TD). Symptoms of EPS include restlessness, tremor, and stiffness. TD symptoms include slow or jerky movements that one cannot control, often starting in the mouth with tongue rolling or chewing movements.

    Temperature regulation: Impaired core body temperature regulation may occur; caution with strenuous exercise, heat exposure, and dehydration.

    Second generation antipsychotics (SGAs) increase the risk of weight gain, high blood sugar, and high cholesterol. This is also known as metabolic syndrome. Your healthcare provider may ask you for a blood sample to check your cholesterol, blood sugar, and hemoglobin A1c (a measure of blood sugar over time) while you take this medication.

    Information on healthy eating and adding exercise to decrease your chances of developing metabolic syndrome may be found at the following sites:

    http://www.helpguide.org/articles/healthy-eating/healthy-eating.htm
    https://www.helpguide.org/home-pages/exercise-fitness.htm
    SGAs have been linked with higher risk of death, strokes, and transient ischemic attacks (TIAs) in elderly people with behavior problems due to dementia.

    All antipsychotics have been associated with the risk of sudden cardiac death due to an arrhythmia (irregular heartbeat). To minimize this risk, antipsychotic medications should be used in the smallest effective dose when the benefits outweigh the risks. Your doctor may order an EKG to monitor for irregular heartbeat.

    Neuroleptic malignant syndrome is a rare, life threatening adverse effect of antipsychotics which occurs in

    All antipsychotics can cause sedation, dizziness, or orthostatic hypotension (a drop in blood pressure when standing up from sitting or lying down). These side effects may lead to falls which could cause bone fractures or other injuries. This risk is higher for people with conditions or other medications that could worsen these effects. If falls or any of these symptoms occur, contact your healthcare provider.

    Are There Any Risks For Taking Lurasidone For Long Periods Of Time?
    Tardive dyskinesia (TD) is a side effect that develops with prolonged use of antipsychotics. Medications such as lurasidone have been shown to have a lower risk of TD compared to older antipsychotics, such as Haldol (haloperidol). If you develop symptoms of TD, such as grimacing, sucking, and smacking of lips, or other movements that you cannot control, contact your healthcare provider immediately. All patients taking either first or second generation antipsychotics should have an Abnormal Involuntary Movement Scale (AIMS) completed regularly by their healthcare provider to monitor for TD.

    Second generation antipsychotics (SGAs) increase the risk of diabetes, weight gain, high cholesterol, and high triglycerides. (See “Serious Side Effects” section for monitoring recommendations).

    What Other Medications May Interact With Lurasidone?
    The following medications may increase the levels and effects of lurasidone: diltiazem (Cardizem®), erythromycin (Ery-Tab®), and fluconazole (Diflucan®). Grapefruit juice may also increase levels of lurasidone.

    The following medications may decrease the levels and effects of lurasidone: carbamazepine (Tegretol®) and phenobarbital.

    How Long Does It Take For Lurasidone To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking lurasidone. It will probably take several weeks to see big enough changes in your symptoms to decide if lurasidone is the right medication for you.

    Antipsychotic treatment is generally needed lifelong for persons with schizophrenia. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Hallucinations, disorganized thinking, and delusions may improve in the first 1-2 weeks
    Sometimes these symptoms do not completely go away
    Motivation and desire to be around other people can take at least 1-2 weeks to improve
    Symptoms continue to get better the longer you take lurasidone
    It may take 2-3 months before you get the full benefit of lurasidone


    Summary Of FDA Black Box Warnings
    Increased mortality in elderly patients with dementia-related psychosis

    Both first generation (typical) and second generation (atypical) antipsychotics are associated with an increased risk of mortality in elderly patients when used for dementia related psychosis.
    Although there were multiple causes of death in studies, most deaths appeared to be due to cardiovascular causes (e.g. sudden cardiac death) or infection (e.g. pneumonia).
    Antipsychotics are not indicated for the treatment of dementia-related psychosis.
    Suicidal thoughts or actions in children and adults

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide.
    Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking medications. This risk may persist until significant remission occurs.
    Patients, their families, and caregivers should be alert to the emergence of anxiety, restlessness, irritability, aggressiveness and insomnia. If these symptoms emerge, they should be reported to the patient’s prescriber or healthcare professional.
    All patients being treated with this medication for depression should watch for and notify their healthcare provider for worsening symptoms, suicidality and unusual changes in behavior, especially during the first few months of treatment.

  • Concerta, Ritalin and others (Methylphenidate or Dexmethylphenidate)

    Brand names:

    Ritalin®, Methylin® (methylphenidate, immediate release)Tablet: 5 mg, 10 mg, 20 mg
    Chewable tablet: 2.5 mg, 5 mg, 10 mg
    Liquid: 5 mg/5 mL and 10 mg/5 mL
    Ritalin LA® (methylphenidate, extended release)Capsule: 10 mg, 20 mg, 30 mg, 40 mg, 60 mg
    Metadate ER®, Ritalin SR® (methylphenidate, extended release, wax matrix)Tablet: 10 mg, 20 mg
    Metadate CD® (methylphenidate, controlled delivery)Capsule: 10 mg, 20 mg, 30 mg, 40 mg, 50 mg, 60 mg
    Methylin ER® (methylphenidate, extended release, methylcellulose base)Tablet: 10 mg, 20 mg
    Aptensio XR® (methylphenidate, extended release)Capsule: 10 mg, 15 mg, 20 mg, 30 mg, 40 mg, 50 mg, 60 mg
    Concerta® (methylphenidate, extended release)Caplet: 18 mg, 27 mg, 36 mg, 54 mg 
    Daytrana® (methylphenidate patch)Patch: 10 mg, 15 mg, 20 mg, 30 mg
    Quillivant XR® (methylphenidate, extended-release oral suspension)Liquid: 25 mg/5 mL
    Quillichew ER® (methylphenidate HCL, extended release, chewable)Chewable tablet: 20 mg, 30 mg, 40 mg
    Focalin® (Dexmethylphenidate, immediate release)Tablets: 2.5 mg, 5 mg, 10 mg
    Focalin XR® (dexmethylphenidate, extended release)Capsule: 5 mg , 10 mg, 15 mg, 20 mg, 25 mg, 30 mg, 35 mg
    Jornay PM® (methylphenidate HCL, extended release)Capsule: 20 mg, 40 mg, 60 mg, 80 mg, 100 mg
    Cotempla XR-ODT® (methylphenidate, extended release)Oral disintegrating tablet: 8.6 mg, 17.3 mg, 25.9 mg
    Generic names: methylphenidate (METH il FEN i date) or dexmethylphenidate (DEX meth il FEN i date)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Are Methylphenidate Or Dexmethylphenidate And What Do They Treat?
    Methylphenidate or dexmethylphenidate are prescription medications that are used to treat children over 6 years old, adolescents, and adults with attention-deficit hyperactivity disorder (ADHD).

    Symptoms of ADHD interfere with an individual’s ability to function at school or work or in social settings and include:

    Inattention (e.g., making careless mistakes, losing things necessary for tasks)
    Hyperactivity (e.g., inability to sit still)
    Impulsivity (e.g., interrupting or intruding on others)
    Hyperactivity is less common in adults. A person may have severe inattention without hyperactivity or impulsivity.

    Methylphenidate or dexmethylphenidate are used in addition to non-medication treatments to manage ADHD symptoms.

    What Is The Most Important Information I Should Know About Methylphenidate Or Dexmethylphenidate?
    Although some symptoms may improve within days of starting methylphenidate or dexmethylphenidate, it may take several weeks before you notice the full benefits of the medication.

    Are There Specific Concerns About Methylphenidate Or Dexmethylphenidate And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider so that he/she can best manage your medications. People living with ADHD who wish to become pregnant face important decisions, each with risks and benefits as they relate to how the illness, medications, and risks to the fetus may interact. This is a complex decision as untreated ADHD has risks to the fetus as well as the mother. Therefore, it is important to discuss this with your doctor and caregivers.

    Regarding breast-feeding, caution is advised since methylphenidate does pass into breast milk and there is limited information available about the safety of dexmethylphenidate while breastfeeding.

    What Should I Discuss With My Healthcare Provider Before Taking Methylphenidate Or Dexmethylphenidate?
    The most bothersome symptoms of your condition
    If you have thoughts of suicide or harming yourself
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require an adjustment in the medication
    Any other psychiatric or medical problems you have, including heart disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you drink alcohol or use drugs
    How Should I Take Methylphenidate Or Dexmethylphenidate?
    Methylphenidate or dexmethylphenidate is usually taken one to three times per day with or without food.

    While the dose usually varies, your healthcare provider will determine the dose that is right for you based upon your response.

    Immediate release formulations should be given two or three times a day to provide symptom coverage throughout the day.
    Extended release and long-acting medications that last for 8 to 12 hours should be taken once a day in the morning. The capsules with beads may be opened if a person has trouble swallowing, however, the beads should be swallowed whole without chewing. If the beads are chewed, too much medicine is absorbed at once and the effects will not last as long.
    The tablet shell from the Concerta® tablet is not changed in the intestines and may appear in the stool intact. It should not be given to individuals with narrowing of the intestines or in those who have undergone stomach bypass surgery.
    The methylphenidate patch should be applied to a clean, hair-free area in the morning before school and removed approximately 9 hours later for an approximate 12-hour duration of action.
    When taking Quillivant XR® (methylphenidate extended release oral suspension), shake the bottle vigorously for at least 10 seconds to make sure the medication is mixed properly. Be sure to use the oral dose dispenser provided and to clean the dispenser after each use.
    When taking Jornay PM®, doses should be administered in the evening.
    When taking Cotempla XR-ODT® ensure hands are dry when removing from the blister packs by peeling back (not pushing through the foil) and administer immediately. Do not chew or crush tablet and allow it to dissolve on the tongue.
    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Methylphenidate Or Dexmethylphenidate?
    If you miss a dose of methylphenidate or dexmethylphenidate, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed.

    Do not take a missed dose after 5:00 PM, as this may interfere with sleep.

    What Should I Avoid While Taking Methylphenidate Or Dexmethylphenidate?
    Avoid drinking alcohol or using illegal drugs while you are taking methylphenidate or dexmethylphenidate. The beneficial effects of the medication may be decreased and adverse effects may be increased.

    What Happens If I Overdose With Methylphenidate Or Dexmethylphenidate?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    Overdosing with methylphenidate or dexmethylphenidate may lead to nausea and vomiting, rapid heart beat, abnormal heart rhythms, paranoia, hallucinations and seizures.

    What Are Possible Side Effects Of Methylphenidate Or Dexmethylphenidate?
    Common side effects

    Upset stomach, loss of appetite, insomnia, and mild anxiety
    Rare side effects

    Contact your healthcare provider if any of the following occur while taking methylphenidate:

    Significant increases in blood pressure or heart rate, shortness of breath, fatigue
    Severe anxiety, panic attacks, mania, hallucinations, paranoia or delusions
    Severe muscle pain, weakness, signs of dehydration, or dark urine
    Prolonged or painful erection
    Changes of feeling or color in your fingers or toes
    Serious side effects

    Medications like methylphenidate or dexmethylphenidate should be avoided in individuals who have a heart defect (structural abnormalities), uncontrolled high blood pressure, or a disorder of the heart or blood vessels.

    Both methylphenidate and dexmethylphenidate are rarely associated with clinically significant increases in blood pressure or heart rate. Blood pressure and heart rate should be monitored before starting medication, and then weekly while adjusting the dose and then every 1 to 3 months or when side effects like “racing heart,” shortness of breath or exercise fatigue becomes problematic.

    Are There Any Risks For Taking Methylphenidate Or Dexmethylphenidate For Long Periods Of Time?
    Methylphenidate or dexmethylphenidate is a Schedule II controlled substance, similar to other stimulant medications, such as amphetamine, mixed amphetamine salts, dextroamphetamine and lisdexamfetamine. There is a risk of physical and/or emotional dependence (addiction) when it is taken for long periods of time.

    Although treatment with these medications can slow growth, many studies have shown that these changes are small, and children may catch-up with growth over time, therefore this should not be a concern for most children. Height, weight, and eating habits should be discussed before treatment starts and regularly during treatment. If you are concerned about a child's growth, discuss other possible treatments with your child's doctor.

    What Other Medications May Interact With Methylphenidate Or Dexmethylphenidate?
    Medications used to treat depression such as tricyclic antidepressants (TCA) and monoamine oxidase inhibitors can interact with these medications resulting in serious reactions, including high body temperature, high blood pressure, and seizures (convulsions). Tell your healthcare provider if you are beginning or have recently discontinued any of these medications.

    Methylphenidate and dexmethylphenidate should not be taken with or within 2 weeks of monoamine oxidase inhibitor antidepressants (MAOIs), including phenelzine (Nardil®), Tranylcypromine (Parnate®), selegiline (Emsam®), and isocarboxazid (Marplan®) or the antibiotic linezolid (Zyvox®). Taking stimulants with or within 2 weeks of MAOIs can result in seizures, fever or dangerously high blood pressure that can lead to death.

    The following medications may increase the levels and/or effects of methylphenidate or dexmethylphenidate:

    Atomoxetine (Strattera®), caffeine, alcohol, phenylephrine, fluoxetine (Prozac®), bupropion (Wellbutrin®), venlafaxine (Effexor®), duloxetine (Cymbalta®), Modafinil (Provigil®), and armodafinil (Nuvigil®)
    Methylphenidate or dexmethylphenidate may increase the levels and effects of: some seizure medications such as phenobarbital or phenytoin, warfarin, and tricyclic antidepressants such as desipramine or clomipramine.

    Methylphenidate or dexmethylphenidate may decrease the levels and effects of: some blood pressure medications such as clonidine, guanfacine, guanethidine and guanadrel.

    How Long Does It Take For Methylphenidate Or Dexmethylphenidate To Work?
    Although you may experience beneficial effects from methylphenidate or dexmethylphenidate within a few days of starting the medication, it often takes several weeks to get the full effect of the medication. Your healthcare provider may also need to adjust gradually the dose to find the dose that works best for you.

    Summary Of FDA Black Box Warnings
    Dependence

    Medications like methylphenidate or dexmethylphenidate should be given cautiously to patients with a history of drug dependence or alcoholism. Chronic abusive use can lead to marked tolerance and psychological dependence. Psychotic episodes can occur, especially when injected. Careful supervision is required during withdrawal from abusive use, since severe depression may occur. Withdrawal following chronic therapeutic use may unmask symptoms of the underlying disorder that may require follow-up.

  • Remeron (Mirtazapine)

    Brand names:

    Remeron®Tablets: 7.5 mg, 15 mg, 30 mg, 45 mg
    Remeron SolTab®Orally disintegrating tablet:  15 mg, 30 mg, 45 mg

    Generic name: mirtazapine (mir TAZ a peen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Mirtazapine And What Does It Treat?
    Mirtazapine is an antidepressant medication that works in the brain. It is approved for the treatment of major depressive disorder (MDD).

    Symptoms of depression include:

    Depressed mood - feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, and helpless
    Loss of interest or pleasure in your usual activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving and thinking in slow motion)
    Suicidal thoughts or behaviors

    What Is The Most Important Information I Should Know About Mirtazapine?
    Do not stop taking mirtazapine, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of mirtazapine may increase your risk for relapse in your symptoms.

    Stopping mirtazapine abruptly may result in one or more of the following withdrawal symptoms: irritability, nausea, dizziness, vomiting, nightmares, headache, and/or paresthesias (prickling, tingling sensation on the skin).

    Depression is also a part of bipolar illness. People with bipolar disorder who take antidepressants may be at risk for "switching" from depression into mania. Symptoms of mania include "high" or irritable mood, very high self-esteem, decreased need for sleep, pressure to keep talking, racing thoughts, being easily distracted, frequently involved in activities with a large risk for bad consequences (for example, excessive buying sprees).

    Medical attention should be sought if serotonin syndrome is suspected. Please refer to serious side effects for signs/symptoms.

    Are There Specific Concerns About Mirtazapine And Pregnancy?
    If you are planning on becoming pregnant, notify your health care provider to best manage your medications. People living with MDD who wish to become pregnant face important decisions. Untreated MDD has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Caution is advised with breastfeeding since mirtazapine does pass into breast milk.

    What Should I Discuss With My Health Care Provider Before Taking Mirtazapine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication
    Any other psychiatric or medical problems you have, including a history of bipolar disorder
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication
    If you are pregnant, plan to become pregnant, or are breastfeeding
    If you drink alcohol or use drugs

    How Should I Take Mirtazapine?
    Mirtazapine is usually taken one time per day at bedtime with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 15 mg to 45 mg. Only your health care provider can determine the correct dose for you.

    Mirtazapine orally disintegrating tablets will dissolve in your mouth within seconds and can be swallowed with or without liquid.

    Mirtazapine orally disintegrating tablets must remain in their original packaging. Open the package with clean dry hands before each dose. Do not try to put tablets in a pillbox if you take the orally disintegrating tablets.

    Consider using a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Mirtazapine?
    If you miss a dose of mirtazapine, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your health care provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Mirtazapine?
    Avoid drinking alcohol or using illegal drugs while you are taking antidepressant medications. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Mirtazapine?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of mirtazapine does not exist.

    What Are The Possible Side Effects Of Mirtazapine?
    Common side effects

    Sedation
    Increased appetite
    Weight gain
    Feeling dizzy
    Increased cholesterol/triglyceride levels

    Rare/serious side effects

    Angle closure glaucoma (symptoms of angle closure glaucoma may include eye pain, changes in vision, swelling or redness in or around eye)

    Agranulocytosis (low white blood cell count) can increase the risk of infection. If you develop symptoms of infection, such as fever, chills, sore throat, swelling of the lining the mouth or other possible signs of infection, contact your prescriber.

    Serotonin syndrome (symptoms may include shivering, diarrhea, confusion, severe muscle tightness, fever, seizures, and death), seizures.

    Are There Any Risks For Taking Mirtazapine For Long Periods Of Time?
    To date, there are no known problems associated with long term use of mirtazapine. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Mirtazapine?
    Mirtazapine should not be taken with or within 2 weeks of taking monoamine oxidase inhibitors (MAOIs). These include phenelzine (Nardil®), tranylcypromine (Parnate®), isocarboxazid (Marplan®), rasagiline (Azilect®), and selegiline (Emsam®).

    Although rare, there is an increased risk of serotonin syndrome when mirtazapine is used with other medications that increase serotonin, such as other antidepressants, migraine medications called “triptans” (e.g., Imitrex®), some pain medications (e.g., tramadol (Ultram®), and the antibiotic linezolid (Zyvox®).

    How Long Does It Take For Mirtazapine To Work?
    Sleep, energy, or appetite may show some improvement within the first 1-2 weeks. Improvement in these physical symptoms can be an important early signal that the medication is working. Depressed mood and lack of interest in activities may need up to 6-8 weeks to fully improve.

    Summary Of FDA Black Box Warnings
    Suicidal thoughts or actions in children and adults

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide. Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking antidepressant medications. This risk may persist until significant remission occurs.

    In short-term studies, antidepressants increased the risk of suicidality in children, adolescents, and young adults when compared to placebo. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24. Adults age 65 and older taking antidepressants have a decreased risk of suicidality. Patients, their families, and caregivers should be alert to the emergence of anxiety, restlessness, irritability, aggressiveness and insomnia. If these symptoms emerge, they should be reported to the patient’s prescriber or health care professional. All patients being treated with antidepressants for any indication should watch for and notify their health care provider for worsening symptoms, suicidality and unusual changes in behavior, especially during the first few months of treatment.

  •  Narcan, Evzio (Naloxone)

    Brand names:Narcan®Nasal spray: 2 mg/0.1 mL, 4 mg/0.1 mL
    Injection: 0.4 mg/1 mL, 1 mg/1 mL
    Evzio®Injection: 2 mg/0.4 mL
    Generic name: Naloxone (na LOKS one)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Naloxone And What Does It Treat?
    Naloxone is a medication designed to rapidly reverse opioid overdose. Naloxone is an opioid antagonist, meaning it binds to the opioid receptors and reverses/block the effects of other opioids such as heroin or certain pain medications (e.g., oxycodone, morphine, hydrocodone). After administering naloxone, you should still immediately seek emergency medical care.

    Naloxone has no effect in people who have not taken opioids.

    Narcan® is a nasal spray form of naloxone. A generic formulation is available. Naloxone is also available as an auto-injectable device with electronic voice instruction system named Evzio®.

    Who Should Have Naloxone On Hand?
    Anyone can carry naloxone on hand in case of emergencies.

    Some populations that may particularly benefit include:

    Anyone who is taking opioids or is at risk of an overdose
    Family, friends, or acquaintances of someone who may be at risk of an opioid overdose
    Healthcare professionals
    First responders, including police, firefighters, and EMTs

    All 50 states and the District of Columbia permit pharmacy-based naloxone dispensing with a prescription from a physician. Most states allow for behind-the-counter (without a prescription) naloxone purchase. Please check with your local pharmacy for pertinent legal information.

    What Is The Most Important Information I Should Know About Naloxone?
    Naloxone is a drug used in an emergency to reverse an opioid overdose. Naloxone is not a replacement for emergency medical care for an overdose. Even if the patient wakes up or improves, you should still seek emergency medical assistance.

    If the patient is opioid-dependent, use of naloxone may cause opioid withdrawal. Signs of opioid withdrawal include body aches, diarrhea, fast heart rate, high blood pressure, fever, and irritability.

    Are There Specific Concerns About Naloxone And Pregnancy?
    There is limited data on naloxone use in pregnant women to inform about drug-associated risk. It is important to discuss the risks and benefits of continued treatment with your doctor and caregivers.

    Naloxone crosses the placenta and may precipitate withdrawal in the fetus, in addition to the opioid-dependent mother. The fetus should be evaluated for signs of distress after naloxone is used.

    Naloxone did not appear to cause birth defects during animal studies.

    There is no information regarding the presence of naloxone in human milk or its effects on breastfed infants or on milk production. Naloxone does not affect prolactin or oxytocin hormone levels.

    What Should I Discuss With My Health Care Provider Before Taking Naloxone?
    If you have allergies to any medications
    Any other psychiatric or medical problems you have, including a history of heart problems
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements)
    Other non-medication treatments you are receiving, such as talk therapy or counseling. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breastfeeding
    If you use illegal drugs or narcotics

    How Do I Identify An Opioid Overdose?
    Signs and symptoms of an opioid overdose may include:

    Loss of consciousness, unusual sleepiness, and/or inability to respond to loud voices or touch
    Breathing problems such as slow, shallow, or cessation of breathing
    The black circle in the center of the eye (pupil) becomes very small (pinpoint pupils)

    Certain people are at an increased risk for an opioid overdose:

    People with opioid use disorder
    People who may have a reduced opioid tolerance (following detoxification, release from incarceration, cessation of treatment)
    People who use prescription opioids, in particular those taking higher doses
    People who use opioids in combination with other sedating substances (such as alcohol or benzodiazepines)
    Household members of people in possession of opioids (including prescription opioids)

    How Should I Administer Naloxone?
    Depending on the state you live in, friends, family members, and others in the community may give naloxone to someone who has overdosed.

    Evzio® is a prefilled auto-injection device. Each device contains a single dose of naloxone and cannot be reused. Once activated, the device provides verbal instruction to the user. The device should be injected into the muscle or skin of the outer thigh and if necessary, Evzio® may be injected through clothing (i.e., pants or jeans). If symptoms return, additional doses may be administered every 2 to 3 minutes until emergency services arrive or the patient responds positively.

    Narcan® is a prefilled nasal spray. It is also available in generic formulation. Each device contains a single dose of naloxone that cannot be reused. When administering the spray, the patient should be placed flat on their back, with their head tilted back, supporting the neck. The first dose is given as one spray into one nostril. If there is no recovery in 2-3 minutes, the dose is repeated in the other nostril. The spray may be repeated every 2 to 3 minutes in alternating nostrils until emergency services arrive or the patient responds positively.

    Naloxone does not take the place of emergency medical care. Emergency medical services should be contacted and CPR may be performed on the patient.

    What Should I Avoid While Taking Naloxone?
    Since naloxone is an opioid blocker designed to rapidly reverse opioid overdose, it can cause withdrawal symptoms if used in patients who are dependent on opioids. It should be used in an emergency situation if a patient is unresponsive and opioid overdose is suspected. Naloxone has no effect in people who have not taken opioids.

    What Are The Possible Side Effects Of Naloxone?
    In patients who has been using opioids regularly, opioid withdrawal symptoms can occur after receiving naloxone. Opioid withdrawal symptoms include: body aches, fever, sweating, running nose, sneezing, goose bumps, yawning, weakness, shivering or trembling, nervousness, restlessness or irritability, diarrhea, nausea, vomiting, stomach cramping, increased blood pressure, and increased heart rate.

    Common side effects of Evzio® include dizziness and injection site redness.

    What Other Medications May Interact With Naloxone?
    Naloxone may interact with certain cough/cold medications and anti-diarrheal medications. Your pharmacist or doctor will help you to determine if other medications you take can interfere with the effects of naloxone.

    How Long Does It Take For Naloxone To Work?
    Depending on the opioids overdosed, naloxone should show a response in 2 to 3 minutes. Otherwise, the medication can be readministered until medical services arrive or the patient responds positively.

    How Should Naloxone Be Stored?
    Naloxone nasal spray and the auto-injectable device should be stored in room temperature. Replace the auto-injectable device if the solution is discolored or contains a precipitate. Do not freeze products.

    Summary Of Black Box Warnings
    There are no FDA black box warnings for naloxone.

  • ReVia (Naltrexone)

    Brand names:

    ReVia®Tablet: 50 mg
    Vivitrol®Intramuscular injection: 380mg
    Generic name: naltrexone (nal TREKS one)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    Medication Assisted Treatment (MAT)
    Medication assisted treatment (MAT) is the use of medications in combination with counseling and behavioral therapies for the treatment of substance use disorders. A combination of medication and behavioral therapies is effective in the treatment of substance use disorders and can help some people to sustain recovery.

    What Is Naltrexone And What Does It Treat?
    Naltrexone is a medication that works in the brain to treat dependence on alcohol or opioids. Naltrexone works by blocking the effect of opioid receptors and decreasing cravings and urges to use alcohol or opioids. This allows people who take the medication to control urges to use and help maintain abstinence from these substances. It is important to combine naltrexone treatment with counseling and other support.

    Symptoms of alcohol and/or opioid dependence include:

    Being unable to quit using alcohol or opioids despite problems with health and relationships.
    Requiring more alcohol or opioids to achieve the same effect
    Presence of withdrawal symptoms (sweating, shaking, nausea, vomiting, diarrhea, confusion, anxiety) when unable to use alcohol or opioids
    Spending the majority of time using or finding a way to use alcohol or opioids
    Having a desire but an inability to decrease the amount of alcohol or opioids used
    Giving up enjoyable activities in order to use alcohol or opioids

    What Is The Most Important Information I Should Know About Naltrexone?
    Do not stop taking naltrexone, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of naltrexone may increase your risk for relapse.

    You must be free of all opioid-containing substances (such as codeine, hydrocodone, oxycodone, morphine, or heroin) for at least 7 to 10 days before beginning naltrexone or you may experience withdrawal symptoms, such as sweating, shaking, nausea or vomiting.

    After stopping naltrexone, you will respond to lower doses of opioids for pain. Do not begin using opioids at the doses you tolerated prior to starting naltrexone. Doing so puts you at risk for respiratory depression.

    Liver injury may occur with naltrexone. This can be monitored through blood tests. Alert your doctor immediately if you experience any yellowing of your skin and/or eyes, severe stomach pain, or severe nausea or vomiting.

    Patients with substance use disorders are at high risk for depression and suicidal thoughts. If you experience any thoughts of self-harm, call 911 or go to your closest emergency room.

    Alert all of your physicians and pharmacists that you are taking naltrexone. Consider keeping a card in your wallet stating you are taking naltrexone to alert caregivers in case of emergency.

    While on naltrexone, opioid pain medicines will not work. Other types of pain medications (such as ibuprofen, naproxen, or acetaminophen) are not affected.

    Are There Specific Concerns About Naltrexone And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with substance use disorders that wish to become pregnant face important decisions and challenges. Active substance use disorders during pregnancy put the fetus at great risk. It is important to discuss the risks and benefits of continued treatment with your doctor and caregivers.

    The effects of naltrexone on the fetus when used in pregnant women are unknown. It is likely that naltrexone crosses the placenta and can be transferred to the fetus. Naltrexone did not appear to cause structural abnormalities during animal studies; however, there appeared to be some behavioral alterations as well as early fetal loss. These results cannot be applied to humans; therefore, naltrexone should only be used in pregnancy if the benefits outweigh the risk to the fetus.

    Breastfeeding while taking naltrexone is not recommended, as it is likely that naltrexone crosses into the breast milk. The effects of naltrexone on the baby are unknown.

    What Should I Discuss With My Health Care Provider Before Taking Naltrexone?
    Symptoms of your condition that bother you the most
    If you have allergies to any medications
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, including a history of liver disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatments you are receiving, such as talk therapy. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breastfeeding
    If you use illegal drugs or narcotics

    How Should I Take Naltrexone?
    Naltrexone is available as an oral tablet and an intramuscular injection. Only your healthcare provider can determine the route of administration and correct dose for you.

    Naltrexone oral tablets are usually taken once daily with or without food. Taking naltrexone tablets with food may decrease stomach upset. Typically, people are given a test dose of 25 mg daily to ensure they can tolerate the medication. If the low dose is tolerated, the dose is increased to 50 mg daily.

    The injection dose is 380 mg given intramuscularly every four weeks. These injections are given by your doctor, nurse, or pharmacist.

    Consider using a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Naltrexone?
    If you miss a dose of oral naltrexone, take it as soon as you remember unless it is closer to the time of your next dose. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Naltrexone?
    Avoid drinking alcohol, using opioid pain medications (such as codeine, hydrocodone, oxycodone, or morphine), or using illegal drugs while you are taking naltrexone. They may increase adverse effects (e.g., sedation) of the medication.

    Keep in mind that some cough syrups may contain opioid pain medication. Discuss all medications with your doctor and pharmacist prior to taking naltrexone.

    What Happens If I Overdose With Naltrexone?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    Evzio® (naloxone) nasal spray can be used to reverse overdose from opioids including methadone. You should always call 911 after giving someone naloxone to treat an overdose. Ask your provider if prescription naloxone is right for you or your family member to have available.

    What Are The Possible Side Effects Of Naltrexone?
    Common side effects

    Nausea, vomiting, headache, dizziness, muscle cramps, changes in appetite, anxiety, restlessness, or trouble sleeping (insomnia) may occur
    Bruising, itching, tenderness, or swelling at the site of injection may occur with the injectable form of naltrexone

    Rare/serious side effects

    Increased blood pressure or heart rate, confusion, depression, nightmares, blurry vision, nasal congestion
    Changes in liver function or liver failure
    Suicidal thoughts have been reported. People experiencing suicidal thoughts while taking naltrexone should contact their provider immediately
    Severe allergic pneumonia has been reported. Patients should contact their provider if they have symptoms of coughing, wheezing, or difficulty breathing

    Are There Any Risks For Taking Naltrexone For Long Periods Of Time?
    To date, there are no known problems associated with long term use of naltrexone. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Naltrexone?
    Naltrexone may decrease the effects of opioid medications, cough/cold medications, and certain anti-diarrheal medications. Do not take larger than recommended doses to achieve effects as this could lead to coma or death.

    Avoid medications that may harm your liver, such as high doses of Tylenol® (acetaminophen). Talk to your healthcare providers about all of the medications you are taking.

    How Long Does It Take For Naltrexone To Work?
    Naltrexone will begin working shortly after taking one dose.

    Summary Of FDA Black Box Warnings
    There are no FDA black box warnings for naltrexone.

  • Trileptal (Oxcarbazepine)

    Brand names: Trileptal®, Oxtellar XR®

    Tablet: 150 mg, 300 mg, 600 mg
    Liquid: 300 mg/5 mL
    Extended-release tablet: 150 mg, 300 mg, 600 mg
    Generic name: oxcarbazepine (ox car BAZ e peen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Oxcarbazepine And What Does It Treat?
    Oxcarbazepine is an antiepileptic medication that works in the brain to prevent and control seizures. It is approved for the treatment of partial seizures.

    Oxcarbazepine may also be helpful when prescribed “off-label” for nerve pain or as a mood stabilizer for bipolar disorder. “Off-label” means that it hasn’t been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an “off-label” treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    Bipolar disorder involves episodes of depression and/or mania.

    Symptoms of depression include:

    Depressed mood — feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, or helpless
    Loss of interest or pleasure in normal activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving in slow motion)
    Symptoms of mania include:

    Feeling irritable or “high”
    Having increased self esteem
    Feeling like you don’t need to sleep
    Feeling the need to continue to talk
    Feeling like your thoughts are too quick (racing thoughts)
    Feeling distracted
    Getting involved in activities that are risky or could have bad consequences (e.g., excessive spending)


    What Is The Most Important Information I Should Know About Oxcarbazepine?
    Bipolar disorder requires long-term treatment. Do not stop taking oxcarbazepine, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine. Missing doses of oxcarbazepine may increase your risk for a relapse in your mood symptoms.

    Do not stop taking oxcarbazepine or change your dose without talking to with your healthcare provider first.

    In order for oxcarbazepine to work properly, it should be taken every day as ordered by your healthcare provider.

    Periodically, your healthcare provider may ask you to provide a blood sample to make sure the appropriate level of medication is in your body and to assess for side effects, such as changes in blood cell counts and sodium levels.

    Are There Specific Concerns About Oxcarbazepine And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider so that he/she can best manage your medications. People living with bipolar disorder who wish to become pregnant face important decisions. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Oxcarbazepine has been associated with an increased risk of craniofacial defects and heart malformations. There may be precautions to decrease the risk of this effect. Do not stop taking oxcarbazepine without first speaking to your healthcare provider. Discontinuing mood stabilizer medications during pregnancy has been associated with a significant increase in symptom relapse.

    Regarding breast-feeding, caution is advised since oxcarbazepine does pass into breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Oxcarbazepine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you drink alcohol or use illegal drugs


    How Should I Take Oxcarbazepine?
    Oxcarbazepine is usually taken once or twice a day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 900-1200 mg per day. People taking this medication for seizure control may take up to 2400 mg daily. Only your healthcare provider can determine the correct dose for you.

    Oxcarbazepine suspension: Measure your dose with a dosing spoon or oral syringe, which you can get from your pharmacy. Before using, shake the bottle well to ensure the medicine is mixed thoroughly. Your dose can be mixed in a small glass of water just prior to taking or may be swallowed directly from the dosing spoon.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Oxcarbazepine?
    If you miss a dose of oxcarbazepine, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your dose or take more than what is prescribed.

    What Should I Avoid While Taking Oxcarbazepine?
    Avoid drinking alcohol or using illegal drugs while you are taking oxcarbazepine. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation, dizziness) of the medication.

    What Happens If I Overdose With Oxcarbazepine?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of oxcarbazepine does not exist.

    What Are Possible Side Effects Of Oxcarbazepine?
    Common side effects

    Dizziness
    Drowsiness
    Vision changes
    Nausea/vomiting
    Headache
    Fatigue
    Uncoordinated movements
    Tremor
    Rare/serious side effects

    Oxcarbazepine can cause a decrease in the body’s sodium level. Some signs of low sodium include nausea, tiredness, lack of energy, headache, confusion, or more frequent or more severe seizures.

    Oxcarbazepine may also cause allergic reactions or serious problems which may affect organs and other parts of your body like the liver or blood cells. You may or may not have a rash with these types of reactions.

    In rare cases (

    Studies have found that individuals who take antiepileptic medications including oxcarbazepine may be twice as likely to have suicidal thoughts or behaviors as individuals who take placebo (inactive medication). These thoughts or behaviors are rare and occurred in approximately 1 in 500 patients taking the antiepileptic class of medications. If you experience any thoughts or impulses to hurt yourself, you should contact your doctor immediately.

    Are There Any Risks For Taking Oxcarbazepine For Long Periods Of Time?
    To date, there are no known problems associated with long term use of oxcarbazepine. It is a safe and effective medication when used as directed.

    It is important to note that some of the side effects listed above (particularly changes in blood sodium, rash, and suicidal thoughts) may continue to occur or worsen if you continue taking the medication. It is important to follow up with your doctor for blood work and to contact your doctor immediately if you notice any skin rash or changes in mood or behavior.

    What Other Medications May Interact With Oxcarbazepine?
    The seizure medications phenobarbital and phenytoin may decrease the effects of oxcarbazepine.

    Oxcarbazepine may increase the effects of phenobarbital and phenytoin.

    Oxcarbazepine may decrease the level and effects of:

    Oral contraceptives (birth control pills)
    Anti-rejection medications used in organ transplants, like tacrolimus (Prograf®) and cyclosporine (Neoral®, Sandimmune®)
    Certain blood pressure medications, such as amlodipine (Norvasc®) or felodipine (Plendil®)


    How Long Does It Take For Oxcarbazepine To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking oxcarbazepine and whether or not you are experiencing any side effects from the medication. It will probably take several weeks to see big enough changes in your symptoms to decide if oxcarbazepine is the right medication for you.

    Mood stabilizer treatment is generally needed lifelong for persons with bipolar disorder. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Summary Of FDA Black Box Warnings
    There are no FDA black box warnings for oxcarbazepine.

  • Invega (Paliperidone)

    Brand names:

    Invega®Extended-release tablet: 1.5 mg, 3 mg, 6 mg, 9 mg
    Invega Sustenna®Extended-release injectable suspension: 39 mg, 78 mg, 117 mg, 156 mg, 234 mg
    Invega Trinza®Extended-release injectable suspension: 273mg, 410mg, 546mg, 819mg
    Generic name: paliperidone (pal ee PER i done)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Paliperidone And What Does It Treat?
    Paliperidone is a medication that works in the brain to treat schizophrenia and schizoaffective disorder. It is also known as a second-generation antipsychotic (SGA) or atypical antipsychotic. Paliperidone rebalances dopamine and serotonin to improve thinking, mood, and behavior.

    Symptoms of schizophrenia/psychosis include:

    Hallucinations — imagined voices or images that seem real
    Delusions — beliefs that are not true (e.g., other people are reading your thoughts)
    Disorganized thinking or trouble organizing your thoughts and making sense
    Little desire to be around other people
    Trouble speaking clearly
    Lack of motivation
    Schizoaffective disorder is an illness that includes abnormal moods (elevated and/or depressed) and psychosis.

    Mood symptoms include:

    Depressed mood — feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, or helpless
    Loss of interest or pleasure in normal activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving in slow motion)
    Feeling irritable or ‘high”
    Having increased self esteem
    Feeling like you don’t need to sleep
    Feeling the need to continue to talk
    Feeling like your thoughts are too quick (racing thoughts)
    Feeling distracted
    Getting involved in activities that are risky or could have bad consequences (e.g. excessive spending)
    Paliperidone may help some or all of these symptoms.

    This medication sheet will focus primarily on schizophrenia. You can find more information about schizoaffective disorder here.

    What Is The Most Important Information I Should Know About Paliperidone?
    Schizophrenia requires long-term treatment. Do not stop taking paliperidone, even when you feel better.

    With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of paliperidone may increase your risk for a relapse in your symptoms.

    Do not stop taking paliperidone or change your dose without talking with your healthcare provider first.

    For paliperidone to work properly, it should be taken every day as ordered by your healthcare provider.

    Are There Specific Concerns About Paliperidone And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with schizophrenia who wish to become pregnant face important decisions. This is a complex decision since untreated schizophrenia has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Antipsychotic use during the third trimester of pregnancy has a risk for abnormal muscle movements (extrapyramidal symptoms [EPS]) and/or withdrawal symptoms in newborns following delivery. Symptoms in the newborn may include agitation, feeding disorder, hypertonia, hypotonia, respiratory distress, somnolence,and tremor; these effects may be self-limiting or require hospitalization.

    Caution is advised with breastfeeding since paliperidone does pass into breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Paliperidone?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you ever had muscle stiffness, shaking, tardive dyskinesia, neuroleptic malignant syndrome, or weight gain caused by a medication
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any psychiatric or medical problems you have, such as heart rhythm problems, long QT syndrome, heart attacks, diabetes, high cholesterol, or seizures
    If you have a family history of diabetes or heart disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you smoke, drink alcohol, or use illegal drugs 


    How Should I Take Paliperidone?
    Paliperidone tablets are usually taken 1 time per day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose of the tablets usually ranges from 3 mg to 12 mg. The dose of the Sustenna brand of long-acting paliperidone injection formulation usually ranges from 78 mg to 234 mg every month. The dose of the Trinza brand long-acting paliperidone injection formulation ranges from 273mg to 819mg every 3 months. Only your healthcare provider can determine the correct dose for you.

    The tablets should be swallowed whole. They should not be chewed, crushed, or broken.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    The Sustenna brand of long-acting injection paliperidone is administered twice in the first 8 days of treatment, then every 4 weeks. Your healthcare provider will administer these injections.

    What Happens If I Miss A Dose Of Paliperidone?
    If you miss a dose of paliperidone, take it as soon as you remember, unless it is closer to the time of your next dose. Do not double your next dose or take more than what is prescribed. If you miss an injection, call your doctor or pharmacist right away. Discuss this with your healthcare provider.

    What Should I Avoid While Taking Paliperidone?
    Avoid drinking alcohol or using illegal drugs while you are taking paliperidone. They may decrease the benefits (e.g. worsen your confusion) and increase adverse effects (e.g. sedation) of the medication.

    What Happens If I Overdose With Paliperidone?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of paliperidone does not exist.

    What Are Possible Side Effects Of Paliperidone?
    Common side effects

    Tachycardia, drowsiness, extrapyramidal symptoms, restlessness, headache, increased prolactin, cholesterol abnormalities, increased glucose, vomiting, tremor

    Rare/serious side effects

    Paliperidone may increase the blood levels of a hormone called prolactin. Side effects of increased prolactin levels include females losing their period, production of breast milk and males losing their sex drive or possibly experiencing erectile problems. Long term (months or years) of elevated prolactin can lead to osteoporosis, or increased risk of bone fractures.

    Some people may develop muscle related side effects while taking paliperidone. The technical terms for these are “extrapyramidal symptoms” (EPS) and “tardive dyskinesia” (TD). Symptoms of EPS include restlessness, tremor, and stiffness. TD symptoms include slow or jerky movements that one cannot control, often starting in the mouth with tongue rolling or chewing movements.

    Temperature regulation: Impaired core body temperature regulation may occur; caution with strenuous exercise, heat exposure, and dehydration.

    Second generation antipsychotics (SGAs) increase the risk of weight gain, high blood sugar, and high cholesterol. This is also known as metabolic syndrome. Your healthcare provider may ask you for a blood sample to check your cholesterol, blood sugar, and hemoglobin A1c (a measure of blood sugar over time) while you take this medication.

    Information on healthy eating and adding exercise to decrease your chances of developing metabolic syndrome may be found at the following sites:

    http://www.helpguide.org/articles/healthy-eating/healthy-eating.htm
    http://www.helpguide.org/home-pages/exercise-fitness.htm
    SGAs have been linked with higher risk of death, strokes, and transient ischemic attacks (TIAs) in elderly people with behavior problems due to dementia.

    All antipsychotics have been associated with the risk of sudden cardiac death due to an arrhythmia (irregular heartbeat). To minimize this risk, antipsychotic medications should be used in the smallest effective dose when the benefits outweigh the risks. Your doctor may order an EKG to monitor for irregular heartbeat.

    Neuroleptic malignant syndrome is a rare, life threatening adverse effect of antipsychotics which occurs in

    All antipsychotics can cause sedation, dizziness, or orthostatic hypotension (a drop in blood pressure when standing up from sitting or lying down). These side effects may lead to falls which could cause bone fractures or other injuries. This risk is higher for people with conditions or other medications that could worsen these effects. If falls or any of these symptoms occur, contact your healthcare provider.

    Are There Any Risks For Taking Paliperidone For Long Periods Of Time?
    Tardive dyskinesia (TD) is a side effect that develops with prolonged use of antipsychotics. Medications such as paliperidone have been shown to have a lower risk of TD compared to older antipsychotics, such as Haldol® (haloperidol). If you develop symptoms of TD, such as grimacing, sucking, and smacking of lips, or other movements that you cannot control, contact your healthcare provider immediately. All patients taking either first or second generation antipsychotics should have an Abnormal Involuntary Movement Scale (AIMS) completed regularly by their healthcare provider to monitor for TD.

    Second generation antipsychotics (SGAs) increase the risk of diabetes, weight gain, high cholesterol, and high triglycerides. (See “Serious Side Effects” section for monitoring recommendations).

    What Other Medications May Interact With Paliperidone?
    Paliperidone may block the effects of agents used to treat Parkinson’s disease such as levodopa (Sinemet®), bromocriptine, pramipexole (Mirapex®), ropinirole (Requip®), and others.

    Paliperidone may lower your blood pressure. Medications used to lower blood pressure may increase this effect and increase your risk of falling.  Propranolol (Inderal®) is an example of this type of medication.

    The following medications may increase the risk of heart problems when used with paliperidone.

    Antipsychotics including chlorpromazine (Thorazine®), thioridizine (Mellaril®), iloperidone (Fanapt®), asenapine (Saphris®), quetiapine (Seroquel®), and ziprasidone (Geodon®).
    Antiarrhythmics (heart rhythm medications), including procainamide, quinidine, amiodarone (Cordarone®), dronedarone (Multaq®), and sotalol (Betapace®).
    The following medications may increase the levels and effects of paliperidone: divalproex sodium (Depakote®).

    The following medications may decrease the levels and effects of paliperidone: carbamazepine (Tegretol®, Equatro®), rifampin, St. John's Wort.

    How Long Does It Take For Paliperidone To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking paliperidone. It will probably take several weeks to see big enough changes in your symptoms to decide if paliperidone is the right medication for you.

    Antipsychotic treatment is generally needed lifelong for persons with schizophrenia. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Hallucinations, disorganized thinking, and delusions may improve in the first 1-2 weeks
    Sometimes these symptoms do not completely go away
    Motivation and desire to be around other people can take at least 1-2 weeks to improve
    Symptoms continue to get better the longer you take paliperidone
    It may take 2-3 months before you get the full benefit of paliperidone


    Summary Of FDA Black Box Warnings
    Increased mortality in elderly patients with dementia-related psychosis

    Both first generation (typical) and second generation (atypical) antipsychotics are associated with an increased risk of mortality in elderly patients when used for dementia related psychosis.
    Although there were multiple causes of death in studies, most deaths appeared to be due to cardiovascular causes (e.g. sudden cardiac death) or infection (e.g. pneumonia).
    Antipsychotics are not indicated for the treatment of dementia-related psychosis.

  • Paxil (Paroxetine)

    Brand names:

    Paxil®Tablets (immediate release): 10 mg, 20 mg, 30 mg, 40 mg
    Liquid suspension: 10 mg/5 mL
    Paxil CR®Tablets (controlled release): 12.5 mg, 25 mg, 37.5 mg
    Pexeva®Tablets (immediate release): 10 mg, 20 mg, 30 mg, 40 mg
    Brisdelle®Capsule: 7.5 mg

    Generic name: paroxetine (pa ROKS e teen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Paroxetine And What Does It Treat?
    Paroxetine is an antidepressant medication that works in the brain. It is approved for the treatment of major depressive disorder (MDD), generalized anxiety disorder (GAD), social anxiety disorder (social phobia), panic disorder, obsessive compulsive disorder (OCD), posttraumatic stress disorder (PTSD), and premenstrual dysphoric disorder (PMDD), and for vasomotor symptoms (hot flashes, night sweats, flushes, etc.) associated with menopause (Brisdelle®).

    Symptoms of depression include:

    Depressed mood - feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, and helpless
    Loss of interest or pleasure in your usual activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving and thinking in slow motion)
    Suicidal thoughts or behaviors

    Generalized Anxiety Disorder (GAD) occurs when a person experiences excessive anxiety or worry for at least six months. Other symptoms include:

    Restlessness
    Fatigue (low energy, feeling tired all the time)
    Difficulty concentrating
    Irritability
    Muscle tension
    Sleep disturbance (difficulty falling asleep or waking up in the middle of the night)

    Obsessive Compulsive Disorder (OCD) occurs when a person experiences the following symptoms at the same time:

    Obsessions (unwanted, recurrent, and disturbing thoughts)
    Compulsions (repetitive, ritualized behaviors that the person feels driven to perform in order to lessen the anxiety produced by the obsession)

    Panic Disorder occurs when a person experiences unexpected and repeated episodes of intense fear. These episodes have physical symptoms including chest pain, shortness of breath, heart palpitations, sweating, dizziness, and nausea. Fear of future episodes is also part of panic disorder.

    PTSD occurs when a person experiences a traumatic event (e.g., assault, combat experience) and then later feels on edge; avoids situations that remind them of the event; and experiences flashbacks or nightmares.

    Premenstrual dysphoric disorder (PMDD) is a condition where a woman experiences depression, tension, and irritability for a few days prior to menstruation that end when menstruation begins. These symptoms are more severe than those of premenstrual syndrome (PMS).

    Social phobia/social anxiety disorder is a fear of situations where one may feel as if they are being judged by others. Symptoms include:

    Blushing
    Difficulty talking
    Nausea
    Sweating
    Shaking

    Paroxetine may also be helpful when prescribed “off-label” for irritable bowel syndrome and obsessive-compulsive disorder in children. “Off-label” means that it hasn't been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending any “off-label” treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Paroxetine?
    Do not stop taking paroxetine, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of paroxetine may increase your risk for relapse in your symptoms.

    Stopping paroxetine abruptly may result in one or more of the following withdrawal symptoms: irritability, nausea, feeling dizzy, vomiting, nightmares, headache, and/or paresthesias (prickling, tingling sensation on the skin).

    Depression is also a part of bipolar illness. People with bipolar disorder who take antidepressants may be at risk for "switching" from depression into mania. Symptoms of mania include "high" or irritable mood, very high self-esteem, decreased need for sleep, pressure to keep talking, racing thoughts, being easily distracted, frequently involved in activities with a large risk for bad consequences (for example, excessive buying sprees).

    Medical attention should be sought if serotonin syndrome is suspected. Please refer to serious side effects for signs/symptoms.

    Are There Specific Concerns About Paroxetine And Pregnancy?
    If you are planning on becoming pregnant, notify your health care provider to best manage your medications. People living with MDD who wish to become pregnant face important decisions. Untreated MDD has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers. Exposure of paroxetine to the fetus during the first trimester of pregnancy can increase the risk of cardiovascular malformations. For women who take antidepressant medications during weeks 13 through the end of their pregnancy (second and third trimesters), there is a risk that the baby can be born before it is fully developed (before 37 weeks).

    For mothers who have taken SSRIs during their pregnancy, there appears to be less than a 1% chance of infants developing persistent pulmonary hypertension. This is a potentially fatal condition that is associated with use of the antidepressant in the second half of pregnancy. However, women who discontinued antidepressant therapy were five times more likely to have a depression relapse than those who continued their antidepressant. If you are pregnant, please discuss the risks and benefits of antidepressant use with your health care provider.

    Caution is advised with breastfeeding since paroxetine does pass into breast milk.

    What Should I Discuss With My Health Care Provider Before Taking Paroxetine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, including a history of bipolar disorder, bone problems, liver or kidney problems, bleeding or heart problems, glaucoma, low sodium in your blood or seizure disorder.
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breastfeeding
    If you drink alcohol or use drugs

    How Should I Take Paroxetine?
    Paroxetine is usually taken one time per day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 10 mg to 40 mg (75 mg for controlled release). Only your health care provider can determine the correct dose for you.

    If you are taking paroxetine for PMDD, it can be taken once daily (everyday) or intermittently (usually starting 14 days prior to menstruation through the first full day of menses of each cycle). Discuss this with your prescriber.

    The liquid should be measured with a dosing spoon or oral syringe which you can get from your pharmacy.

    The controlled release form as well as Pexeva® should be swallowed whole. They should not be chewed, crushed, or broken.

    Consider using a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Paroxetine?
    If you miss a dose of paroxetine, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your health care provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Paroxetine?
    Avoid drinking alcohol or using illegal drugs while you are taking antidepressant medications. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Paroxetine?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of paroxetine does not exist.

    What Are The Possible Side Effects Of Paroxetine?
    Common side effects

    Headache, nausea, constipation, diarrhea, dry mouth, increased sweating, and dizziness
    Feeling nervous, restless, fatigued, sleepy or having trouble sleeping (insomnia)
    These will often improve over the first week or two as you continue to take the medication.

    Sexual side effects, such as problems with orgasm or ejaculatory delay often do not diminish over time.

    Rare/serious side effects

    Low sodium blood levels (symptoms of low sodium levels may include headache, weakness, difficulty concentrating and remembering), teeth grinding, angle closure glaucoma (symptoms of angle closure glaucoma may include eye pain, changes in vision, swelling or redness in or around eye)

    Serotonin syndrome (symptoms may include shivering, diarrhea, confusion, severe muscle tightness, fever, seizures, and death), seizure

    Discontinuation syndrome (abrupt discontinuation may include nausea, sweating, dysphoric mood, irritability, agitation, dizziness, sensory disturbances as electric shock sensations, tremor, anxiety, confusion, headache, lethargy, emotional lability, insomnia, hypomania, ringing in the ears, and seizures.

    SSRI antidepressants including paroxetine may increase the risk of bleeding events. Combined use of aspirin, nonsteroidal anti-inflammatory drugs (e.g., ibuprofen, naproxen), warfarin, and other anti-coagulants may increase this risk. This may include gums that bleed more easily, nosebleed, or gastrointestinal bleeding. Some cases have been life threatening.

    Hypersensitivity to paroxetine. Call your health care provider if you get rash, hives, swelling, or difficulty breathing. Avoid with known hypersensitivity to paroxetine or any ingredients mixed with it.

    Are There Any Risks For Taking Paroxetine For Long Periods Of Time?
    To date, there are no known problems associated with long term use of paroxetine. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Paroxetine?
    Paroxetine should not be taken with or within two weeks of taking monoamine oxidase inhibitors (MAOIs). These include phenelzine (Nardil®), tranycypromine (Parnate®), isocarboxazid (Marplan®), rasagiline (Azilect®), and selegiline (Emsam®).

    Although rare, there is an increased risk of serotonin syndrome when paroxetine is used with other medications that increase serotonin, such as other antidepressants, buspirone (Buspar), lithium (Lithobid) migraine medications called “triptans” (e.g., Imitrex®), some pain medications (e.g., tramadol (Ultram®)), the antibiotic linezolid (Zyvox®), or intravenous methylene blue.

    Paroxetine may increase the levels of:

    Atomoxetine (Stratterra®)
    Antipsychotics, such as aripiprazole (Abilify®), risperidone (Risperdal®)
    Warfarin (Coumadin®)
    Cardiac medications such as propafenone (Rythmol®), metoprolol (Toprol XL®, Lopressor®) and propranolol (Inderal®)
    Tricyclic antidepressants, such as, desipramine (Norpramin®), imipramine (Tofranil®)

    Combining paroxetine with thioridazine (Mellaril®), tamoxifen (Soltamox), pimozide (Orap) is not recommended.

    Paroxetine may increase the effects of other medications that can cause bleeding (e.g., ibuprofen (Advil®, Motrin®), warfarin (Coumadin®) and aspirin).

    How Long Does It Take For Paroxetine To Work?
    Sleep, energy, or appetite may show some improvement within the first 1-2 weeks. Improvement in these physical symptoms can be an important early signal that the medication is working. Depressed mood and lack of interest in activities may need up to 6-8 weeks to fully improve.

    Summary Of FDA Black Box Warnings
    Suicidal thoughts or actions in children and adults

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide. Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether they are taking antidepressant medications. This risk may persist until significant remission occurs.

    In short-term studies, antidepressants increased the risk of suicidality in children, adolescents, and young adults when compared to placebo. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24. Adults age 65 and older taking antidepressants have a decreased risk of suicidality. Patients, their families, and caregivers should be alert to the emergence of anxiety, restlessness, irritability, aggressiveness and insomnia. If these symptoms emerge, they should be reported to the patient’s prescriber or health care professional. All patients being treated with antidepressants for any indication should watch for and notify their health care provider for worsening symptoms, suicidality and unusual changes in behavior, especially during the first few months of treatment.

    Paroxetine extended release is not approved for use in pediatric patients.

  • Seroquel (Quetiapine)

    Brand names:

    Seroquel®Tablet (immediate release): 25 mg, 50 mg, 100 mg, 200 mg, 300 mg, 400 mg
    Seroquel XR®Tablet (extended release): 50 mg, 150 mg, 200 mg, 300 mg, 400 mg
    Generic name: quetiapine (kwe TYE a peen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Quetiapine And What Does It Treat?
    Quetiapine is a medication that works in the brain to treat schizophrenia. It is also known as a second generation antipsychotic (SGA) or atypical antipsychotic. Quetiapine rebalances dopamine and serotonin to improve thinking, mood, and behavior.

    Symptoms of schizophrenia include:

    Hallucinations — imagined voices or images that seem real
    Delusions — beliefs that are not true (e.g., other people are reading your thoughts)
    Disorganized thinking or trouble organizing your thoughts and making sense
    Little desire to be around other people
    Trouble speaking clearly
    Lack of motivation
    Quetiapine may help some or all of these symptoms.

    Quetiapine is also FDA approved for the following indications:

    Acute treatment of manic episodes of bipolar disorder
    Acute treatment of depressive episodes of bipolar disorder
    Maintenance (long-term) treatment of bipolar disorder (when used alone or with lithium or valproate)
    Adjunctive treatment of major depressive disorder. This means quetiapine is used in addition to an antidepressant to help treat depression.
    This medication sheet will focus primarily on schizophrenia. You can find more information about bipolar disorder and depression here.

    Quetiapine may also be helpful when prescribed "off-label" for delusional parasitosis, post-traumatic stress disorder (PTSD), generalized anxiety disorder, delirium in the intensive care unit, and obsessive compulsive disorder. "Off-label" means that it has not been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an "off-label" treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Quetiapine?
    Schizophrenia requires long-term treatment. Do not stop taking quetiapine, even when you feel better.

    With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of quetiapine may increase your risk for a relapse in your symptoms.

    Do not stop taking quetiapine or change your dose without talking with your healthcare provider first.

    For quetiapine to work properly, it should be taken every day as ordered by your healthcare provider.

    Are There Specific Concerns About Quetiapine And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with schizophrenia who wish to become pregnant face important decisions. This is a complex decision since untreated schizophrenia has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Antipsychotic use during the third trimester of pregnancy has a risk for abnormal muscle movements (extrapyramidal symptoms [EPS]) and/or withdrawal symptoms in newborns following delivery. Symptoms in the newborn may include agitation, feeding disorder, hypertonia, hypotonia, respiratory distress, somnolence, and tremor; these may be self-limiting or require hospitalization.

    Caution is advised with breastfeeding since quetiapine does pass into breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Quetiapine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you ever had muscle stiffness, shaking, tardive dyskinesia, neuroleptic malignant syndrome, or weight gain caused by a medication
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any psychiatric or medical problems you have, such as heart rhythm problems, long QT syndrome, heart attacks, diabetes, high cholesterol, or seizures
    If you have a family history of diabetes or heart disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you smoke, drink alcohol, or use illegal drugs


    How Should I Take Quetiapine?
    Quetiapine is usually taken 1, 2, or 3 times per day with or without food. The extended release should be taken without food or with a light meal (≤300 calories).

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 100 mg to 800 mg. Only your healthcare provider can determine the correct dose for you.

    The extended release tablets should be swallowed whole. They should not be chewed, crushed, or broken.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Quetiapine?
    If you miss a dose of quetiapine, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Quetiapine?
    Avoid drinking alcohol or using illegal drugs while you are taking quetiapine. They may decrease the benefits (e.g. worsen your confusion) and increase adverse effects (e.g. sedation) of the medication.

    What Happens If I Overdose With Quetiapine?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of quetiapine does not exist.

    What Are Possible Side Effects Of Quetiapine?
    Common side effects

    Increased blood pressure, increased heart rate, drowsiness, headache, agitation, dizziness, fatigue, extrapyramidal symptoms, weight gain, cholesterol abnormalities, increased glucose, dry mouth, increased appetite, constipation

    Rare/serious side effects

    Quetiapine may increase the blood levels of a hormone called prolactin. Side effects of increased prolactin levels include females losing their period, production of breast milk and males losing their sex drive or possibly experiencing erectile problems. Long term (months or years) of elevated prolactin can lead to osteoporosis, or increased risk of bone fractures.

    Some people may develop muscle related side effects while taking quetiapine. The technical terms for these are “extrapyramidal symptoms” (EPS) and “tardive dyskinesia” (TD). Symptoms of EPS include restlessness, tremor, and stiffness. TD symptoms include slow or jerky movements that one cannot control, often starting in the mouth with tongue rolling or chewing movements.

    Temperature regulation: Impaired core body temperature regulation may occur; caution with strenuous exercise, heat exposure, and dehydration.

    Second generation antipsychotics (SGAs) increase the risk of weight gain, high blood sugar, and high cholesterol. This is also known as metabolic syndrome. Your healthcare provider may ask you for a blood sample to check your cholesterol, blood sugar, and hemoglobin A1c (a measure of blood sugar over time) while you take this medication.

    Information on healthy eating and adding exercise to decrease your chances of developing metabolic syndrome may be found at the following sites:

    http://www.helpguide.org/articles/healthy-eating/healthy-eating.htm
    http://www.helpguide.org/home-pages/exercise-fitness.htm
    SGAs have been linked with higher risk of death, strokes, and transient ischemic attacks (TIAs) in elderly people with behavior problems due to dementia.

    All antipsychotics have been associated with the risk of sudden cardiac death due to an arrhythmia (irregular heartbeat). To minimize this risk, antipsychotic medications should be used in the smallest effective dose when the benefits outweigh the risks. Your doctor may order an EKG to monitor for irregular heartbeat.

    Neuroleptic malignant syndrome is a rare, life threatening adverse effect of antipsychotics which occurs in

    All antipsychotics can cause sedation, dizziness, or orthostatic hypotension (a drop in blood pressure when standing up from sitting or lying down). These side effects may lead to falls which could cause bone fractures or other injuries. This risk is higher for people with conditions or other medications that could worsen these effects. If falls or any of these symptoms occur, contact your healthcare provider.

    Are There Any Risks For Taking Quetiapine For Long Periods Of Time?
    Tardive dyskinesia (TD) is a side effect that develops with prolonged use of antipsychotics. Medications such as quetiapine have been shown to have a lower risk of TD compared to older antipsychotics, such as Haldol® (haloperidol). If you develop symptoms of TD, such as grimacing, sucking, and smacking of lips, or other movements that you cannot control, contact your healthcare provider immediately. All patients taking either first or second generation antipsychotics should have an Abnormal Involuntary Movement Scale (AIMS) completed regularly by their healthcare provider to monitor for TD.

    Second generation antipsychotics (SGAs) increase the risk of diabetes, weight gain, high cholesterol, and high triglycerides. (See “Serious Side Effects” section for monitoring recommendations).

    What Other Medications May Interact With Quetiapine?
    Quetiapine may block the effects of agents used to treat Parkinson’s disease such as levodopa/carbidopa (Sinemet®), bromocriptine, pramipexole (Mirapex®), ropinirole (Requip®), and others.

    The following medications may increase the risk of heart problems when used with quetiapine:

    Antipsychotics, including chlorpromazine (Thorazine®), thioridizine (Mellaril®), iloperidone (Fanapt®), asenapine (Saphris®), paliperidone (Invega®), ziprasidone (Geodon®)
    Antiarrhythmics (heart rhythm medications), including procainamide, quinidine, amiodarone (Cordarone®), dronedarone (Multaq®), sotalol (Betapace®)
    The following medications may increase the levels and effects of quetiapine:

    Erythromycin (Ery-Tab®), fluconazole (Diflucan®), fluvoxamine (Luvox®), and nefazodone.
    The following medications may decrease the levels and effects of quetiapine:

    Carbamazepine (Tegretol®), phenytoin (Dilantin®), phenobarbital, and rifampin (Rifadin®).
    How Long Does It Take For Quetiapine To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking quetiapine. It will probably take several weeks to see big enough changes in your symptoms to decide if quetiapine is the right medication for you.

    Antipsychotic treatment is generally needed lifelong for persons with schizophrenia. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Hallucinations, disorganized thinking, and delusions may improve in the first 1-2 weeks
    Sometimes these symptoms do not completely go away
    Motivation and desire to be around other people can take at least 1-2 weeks to improve
    Symptoms continue to get better the longer you take quetiapine
    It may take 2-3 months before you get the full benefit of quetiapine


    Summary Of FDA Black Box Warnings
    Increased mortality in elderly patients with dementia-related psychosis

    Both first generation (typical) and second generation (atypical) antipsychotics are associated with an increased risk of mortality in elderly patients when used for dementia related psychosis.
    Although there were multiple causes of death in studies, most deaths appeared to be due to cardiovascular causes (e.g. sudden cardiac death) or infection (e.g. pneumonia).
    Antipsychotics are not indicated for the treatment of dementia-related psychosis.
    Suicidal thoughts or actions in children and adults

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide.
    Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking medications. This risk may persist until significant remission occurs.
    Patients, their families, and caregivers should be alert to the emergence of anxiety, restlessness, irritability, aggressiveness and insomnia. If these symptoms emerge, they should be reported to the patient’s prescriber or healthcare professional.
    All patients being treated with this medication for depression should watch for and notify their healthcare provider for worsening symptoms, suicidality and unusual changes in behavior, especially during the first few months of treatment.

  • Risperdal (Risperidone)

    Brand names:

    Risperdal®Tablet: 0.25 mg, 0.5 mg, 1 mg, 2 mg, 3 mg, 4 mg
    Orally disintegrating tablet: 0.25 mg, 0.5 mg, 1 mg, 2 mg, 3 mg, 4 mg
    Solution: 1 mg/ml
    Risperdal Consta®Extended-release injectable suspension: 12.5 mg, 25 mg, 37.5 mg, 50 mg
    ​Perseris®Extended-release injectable suspension: 90mg, 120 mg
    Generic name: risperidone (ris PER i done)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Risperidone And What Does It Treat?
    Risperidone is a medication that works in the brain to treat schizophrenia. It is also known as a second generation antipsychotic (SGA) or atypical antipsychotic. Risperidone rebalances dopamine and serotonin to improve thinking, mood, and behavior.

    Symptoms of schizophrenia include:

    Hallucinations — imagined voices or images that seem real
    Delusions — beliefs that are not true (e.g., other people are reading your thoughts)
    Disorganized thinking or trouble organizing your thoughts and making sense
    Little desire to be around other people
    Trouble speaking clearly
    Lack of motivation
    Risperidone may help some or all of these symptoms.

    Risperidone is also FDA approved for the following indications:

    Acute treatment of manic or mixed episodes of bipolar disorder
    Maintenance (long-term) treatment of bipolar disorder
    Irritability associated with autistic disorders
    This medication sheet will focus primarily on schizophrenia. Find more information about bipolar disorder and autism spectrum disorders here.

    Risperidone may also be helpful when prescribed “off-label” for adjunctive treatment of major depression disorder (risperidone is used in addition to an antidepressant), delusional parasitosis, post-traumatic stress disorder (PTSD), Tourette syndrome, and other mental health conditions. “Off-label” means that it has not been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an “off-label” treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Risperidone?
    Schizophrenia requires long-term treatment. Do not stop taking risperidone, even when you feel better.

    With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of risperidone may increase your risk for a relapse in your symptoms.

    Do not stop taking risperidone or change your dose without talking to with your healthcare provider first.

    For risperidone to work properly, the tablet form should be taken every day as ordered by your healthcare provider. One of the long-acting injectable forms, known as Risperdal Consta®, should be received every 2 weeks as ordered by your healthcare provider. The other long-acting injectable form, known as Perseris®, should be received every month. Both of the long-acting injections are the same medication as in the tablet form.

    Are There Specific Concerns About Risperidone And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with schizophrenia who wish to become pregnant face important decisions. This is a complex decision since untreated schizophrenia has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Antipsychotic use during the third trimester of pregnancy has a risk for abnormal muscle movements (extrapyramidal symptoms [EPS]) and/or withdrawal symptoms in newborns following delivery. Symptoms in the newborn may include agitation, feeding disorder, hypertonia, hypotonia, respiratory distress, somnolence, and tremor; these effects may be self-limiting or require hospitalization.

    Caution is advised with breastfeeding since risperidone does pass into breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Risperidone?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you ever had muscle stiffness, shaking, tardive dyskinesia, neuroleptic malignant syndrome, or weight gain caused by a medication
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any psychiatric or medical problems you have, such as heart rhythm problems, long QT syndrome, heart attacks, diabetes, high cholesterol, or seizures
    If you have a family history of diabetes or heart disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you smoke, drink alcohol, or use illegal drugs


    How Should I Take Risperidone?
    Risperidone tablets and solution are usually taken 1 or 2 times per day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The oral dose usually ranges from 1mg to 6 mg. The dose of the injection usually ranges from 12.5 mg to 50 mg. Only your healthcare provider can determine the correct dose for you.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    Risperidone orally disintegrating tablets must remain in their original packaging. Open the package with clean dry hands before each dose. Do not try to put tablets in a pillbox if you take the orally disintegrating tablets.

    Risperidone orally disintegrating tablets will dissolve in your mouth within seconds and can be swallowed with or without liquid.

    Risperidone liquid should be measured with a dosing spoon or oral syringe, which you can get from your pharmacy.

    Risperdal Consta® (risperidone long-acting injection) should be received every 2 weeks. It should be administered by your health care professional through an injection into your upper arm or buttocks area. The medication effects last for approximately 2 weeks. If you are new to taking Risperdal Consta® (risperidone long-acting injection), your health care provider may want you to take the tablet form or risperidone daily for up to 3 weeks.

    Perseris® (risperidone long-acting injection) should be received every month. It should be administered by your health care professional through an injection under the skin of your abdominal area. After establishing tolerability with oral risperidone, you may be switched to Perseris® (risperidone long-acting injection). Supplemental oral risperidone is not recommended after receiving your first Perseris® (risperidone long-acting injection) dose. After receiving the injection, you may have a lump for several weeks that will decrease in size over time. It is important that you not rub or massage the injection site and to be aware of the placement of any belts or clothing waistbands.

    What Happens If I Miss A Dose Of Risperidone?
    If you miss a dose of risperidone, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed. If you miss a dose of Risperdal Consta® or Perseris® (risperidone long-acting injections), see your healthcare provider to receive your dose as soon as possible.

    What Should I Avoid While Taking Risperidone?
    Avoid drinking alcohol or using illegal drugs while you are taking risperidone. They may decrease the benefits (e.g., worsen your confusion) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Risperidone?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of risperidone does not exist.

    What Are Possible Side Effects Of Risperidone?
    Common side effects

    Sedation, drowsiness, extrapyramidal symptoms, insomnia, fatigue, headache, anxiety, dizziness, drooling, restlessness, increased prolactin, weight gain, increased appetite, vomiting, constipation, upper abdominal pain, nausea, urinary incontinence, tremor, cold symptoms, cough, runny nose, fever

    Risperdal Consta® (risperidone long-acting injection): injection site pain

    Perseris® (risperidone long-acting injection): injection site pain, redness, and a lump that may be present for several weeks

    Rare/serious side effects

    Risperidone may increase the blood levels of a hormone called prolactin. Side effects of increased prolactin levels include females losing their period, production of breast milk and males losing their sex drive or possibly experiencing erectile problems. Long term (months or years) of elevated prolactin can lead to osteoporosis, or increased risk of bone fractures.

    Some people may develop muscle related side effects while taking risperidone. The technical terms for these are “extrapyramidal symptoms” (EPS) and “tardive dyskinesia” (TD). Symptoms of EPS include restlessness, tremor, and stiffness. TD symptoms include slow or jerky movements that one cannot control, often starting in the mouth with tongue rolling or chewing movements.

    Temperature regulation: Impaired core body temperature regulation may occur; caution with strenuous exercise, heat exposure, and dehydration.

    Second generation antipsychotics (SGAs) increase the risk of weight gain, high blood sugar, and high cholesterol. This is also known as metabolic syndrome. Your healthcare provider may ask you for a blood sample to check your cholesterol, blood sugar, and hemoglobin A1c (a measure of blood sugar over time) while you take this medication.

    Information on healthy eating and adding exercise to decrease your chances of developing metabolic syndrome may be found at the following sites:

    http://www.helpguide.org/articles/healthy-eating/healthy-eating.htm
    http://www.helpguide.org/home-pages/exercise-fitness.htm
    SGAs have been linked with higher risk of death, strokes, and transient ischemic attacks (TIAs) in elderly people with behavior problems due to dementia.

    All antipsychotics have been associated with the risk of sudden cardiac death due to an arrhythmia (irregular heartbeat). To minimize this risk, antipsychotic medications should be used in the smallest effective dose when the benefits outweigh the risks. Your doctor may order an EKG to monitor for irregular heartbeat.

    Neuroleptic malignant syndrome is a rare, life threatening adverse effect of antipsychotics which occurs in

    All antipsychotics can cause sedation, dizziness, or orthostatic hypotension (a drop in blood pressure when standing up from sitting or lying down). These side effects may lead to falls which could cause bone fractures or other injuries. This risk is higher for people with conditions or other medications that could worsen these effects. If falls or any of these symptoms occur, contact your healthcare provider.

    Are There Any Risks For Taking Risperidone For Long Periods Of Time?
    Tardive dyskinesia (TD) is a side effect that develops with prolonged use of antipsychotics. Medications such as risperidone have been shown to have a lower risk of TD compared to older antipsychotics, such as Haldol® (haloperidol). If you develop symptoms of TD, such as grimacing, sucking, and smacking of lips, or other movements that you cannot control, contact your healthcare provider immediately. All patients taking either first or second generation antipsychotics should have an Abnormal Involuntary Movement Scale (AIMS) completed regularly by their healthcare provider to monitor for TD.

    Second generation antipsychotics (SGAs) increase the risk of diabetes, weight gain, high cholesterol, and high triglycerides. (See “Serious Side Effects” section for monitoring recommendations).

    What Other Medications May Interact With Risperidone?
    Risperidone may block the effects of agents used to treat Parkinson’s disease such as levodopa/carbidopa (Sinemet®), bromocriptine, pramipexole (Mirapex®), ropinirole (Requip®), and others.

    Risperidone may lower your blood pressure. Medications used to lower blood pressure may increase this effect and increase your risk of falling. Propranolol (Inderal®) is an example of this type of medication.

    The following medications may increase the levels and effects of risperidone: divalproex sodium (Depakote®), fluoxetine (Prozac®), paroxetine (Paxil®), and verapamil (Calan®).

    The following medications may decrease the levels and effects of risperidone: carbamazepine (Tegretol®, Equetro®), phenytoin (Dilantin®), phenobarbital, or rifampin (Rifadin®).

    How Long Does It Take For Risperidone To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking risperidone. It will probably take several weeks to see big enough changes in your symptoms to decide if risperidone is the right medication for you. If you take Risperdal Consta® (risperidone long-acting injection), it will take about three weeks before risperidone is fully absorbed and at an adequate level to begin treating your symptoms. After starting Risperdal Consta® (risperidone long-acting injection) for the first time, or re-starting it after a time of no medication, it is important to continue taking risperidone tablets for at least three weeks. If you take Perseris® (risperidone long-acting injection), it is not recommended to take oral risperidone after the first injection.

    Antipsychotic treatment is generally needed lifelong for persons with schizophrenia. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Hallucinations, disorganized thinking, and delusions may improve in the first 1-2 weeks
    Sometimes these symptoms do not completely go away
    Motivation and desire to be around other people can take at least 1-2 weeks to improve
    Symptoms continue to get better the longer you take risperidone
    It may take 2-3 months before you get the full benefit of risperidone


    Summary Of FDA Black Box Warnings
    Increased mortality in elderly patients with dementia-related psychosis

    Both first generation (typical) and second generation (atypical) antipsychotics are associated with an increased risk of mortality in elderly patients when used for dementia related psychosis.
    Although there were multiple causes of death in studies, most deaths appeared to be due to cardiovascular causes (e.g. sudden cardiac death) or infection (e.g. pneumonia).
    Antipsychotics are not indicated for the treatment of dementia-related psychosis.

  • Topamax (Topiramate)

    Brand names:

    Topamax®Tablet: 25 mg, 50 mg, 100 mg, 200 mg
    Sprinkle capsule: 15 mg, 25 mg
    Trokendi XR®Extended release capsule: 25 mg, 50 mg, 100 mg, 200 mg
    Generic name: topiramate (toe PYRE a mate)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Topiramate And What Does It Treat?
    Topiramate is a medication that works in the brain and is sometimes used in patients with bipolar disorder (also known as manic depression). It is approved for the treatment of seizures (epilepsy) in adults and children in combination with other anticonvulsants and for preventing migraine headaches in adults. Bipolar disorder involves episodes of depression and/or mania.

    Symptoms of depression include:

    Depressed mood — feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, or helpless
    Loss of interest or pleasure in normal activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving in slow motion)
    Symptoms of mania include:

    Feeling irritable or “high”
    Having increased self esteem
    Feeling like you don’t need to sleep
    Feeling the need to continue to talk
    Feeling like your thoughts are too quick (racing thoughts)
    Feeling distracted
    Getting involved in activities that are risky or could have bad consequences (e.g., excessive spending)


    What Is The Most Important Information I Should Know About Topiramate?
    Bipolar disorder requires long-term treatment. Do not stop taking topiramate even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine. Missing doses of topiramate may increase your risk for a relapse in your mood symptoms.

    Do not stop taking topiramate or change your dose without talking to with your healthcare provider first.

    In order for topiramate to work properly, it should be taken every day as ordered by your healthcare provider.

    Are There Specific Concerns About Topiramate And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider so that he/she can best manage your medications. People living with bipolar disorder who wish to become pregnant face important decisions. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Topiramate has been associated with an increased risk of oral cleft birth defects. There may be precautions to decrease the risk of this effect. Do not stop taking topiramate without first speaking to your healthcare provider. Discontinuing similar medications during pregnancy has been associated with a significant increase in symptom relapse.

    Breastfeeding is not recommended in women who are taking topiramate.

    What Should I Discuss With My Healthcare Provider Before Taking Topiramate?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you drink alcohol or use illegal drugs


    How Should I Take Topiramate?
    Topiramate is usually taken one or two times a day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 25 mg to 400 mg. Only your healthcare provider can determine the correct dose for you.

    Do not split or chew tablets as they have a bitter taste.

    Sprinkle capsules: Swallow whole or sprinkle onto food, such as applesauce or pudding and eat immediately. Do not chew the sprinkle capsule or contents.

    Extended-release capsules: Swallow whole. Do not sprinkle on food, chew, or crush capsule.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Topiramate?
    If you miss a dose of topiramate, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your dose or take more than what is prescribed.

    What Should I Avoid While Taking Topiramate?
    Avoid drinking alcohol or using illegal drugs while you are taking topiramate. They may decrease the benefits (e.g., worsen your symptoms) and increase adverse effects (e.g., sedation, dizziness).

    What Happens If I Overdose With Topiramate?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of topiramate does not exist.

    What Are Possible Side Effects Of Topiramate?
    Common side effects

    Thinking problems: slow thoughts, trouble finding the right word, confusion, trouble concentrating
    Feel clumsy, unsteady, dizzy, tired, weak, or nervous
    Loss of appetite, change in the way food tastes, weight loss, stomach pain
    Numbness or tingling sensation in limbs and extremities


    Rare/serious side effects

    Mood or behavior changes, such as aggression, agitation, apathy, irritability, and depression
    Hearing problems (ringing, buzzing, and decreased hearing)
    Fever, sore throat, upper respiratory infection
    Itching, nosebleeds, pale skin, blisters, allergy (skin rash, swelling, troubled breathing), yellow eyes or skin, easy bruising and bleeding
    Topiramate may cause eye problems. Serious eye problems include a sudden decrease in vision with or without pain/redness and increased pressure in the eye. These eye problems can lead to permanent vision loss if not treated.
    Topiramate may cause decreased sweating and increased body temperature. People, especially children, should be watched for signs of this — especially in hot climates. Some people may need to be hospitalized for this condition.
    Topiramate can increase the level of acid in your blood (metabolic acidosis). If left untreated, metabolic acidosis can cause brittle or soft bones, kidney stones, can slow the rate of growth in children, and may possibly harm your baby if you are pregnant. Metabolic acidosis can happen with or without symptoms. Sometimes people with metabolic acidosis will feel tired, not feel hungry, feel changes in heartbeat, or have trouble thinking clearly.
    Studies have found that individuals who take antiepileptic medications, including topiramate, have suicidal thoughts or behaviors up to twice as often as individuals who take placebo (inactive medication). These thoughts or behaviors occurred in approximately 1 in 500 patients taking the antiepileptic class of medications.
    Are There Any Risks For Taking Topiramate For Long Periods Of Time?
    To date, there are no known problems associated with long term use of topiramate. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Topiramate?
    Topiramate may decrease the levels and effects of oral contraceptives (birth control pills).

    The following medications may decrease levels and effects of topiramate: carbamazepine (Tegretol®), phenytoin (Dilantin®), valproate (Depakote®) and phenobarbital

    Combining valproate (Depakote®) with topiramate may increase ammonia levels in your blood. If this happens, you may get confused, disoriented, or have difficulty thinking.

    Carbonic anhydrase inhibitors, including acetazolamide, dichlorphenamide, methazolamide, and dorzolamide, increase the risk of kidney stones when taken with topiramate.

    How Long Does It Take For Topiramate To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking topiramate. It will probably take several weeks to see big enough changes in your symptoms to decide if topiramate is the right medication for you.

    Mood stabilizer treatment is generally needed lifelong for persons with bipolar disorder. Your doctor can best discuss the duration of treatment you need based on your symptoms and course of illness.

    Summary Of FDA Black Box Warnings
    There are no FDA Black Box Warnings for topiramate.

  • Parnate (Tranylcypromine)

    Brand name: Parnate®

    Tablets: 10 mg

    Generic name: Tranylcypromine (tran il SIP roe meen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Tranylcypromine And What Does It Treat?
    Tranylcypromine is an antidepressant medication that works in the brain. It is approved for the treatment of major depressive disorder (MDD).

    Symptoms of depression include:

    Depressed mood - feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, and helpless
    Loss of interest or pleasure in your usual activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving and thinking in slow motion)
    Suicidal thoughts or behaviors

    What Is The Most Important Information I Should Know About Tranylcypromine?
    Do not stop taking tranylcypromine, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of tranylcypromine may increase your risk for relapse in your symptoms.

    Stopping tranylcypromine abruptly may result in one or more of the following withdrawal symptoms: irritability, nausea, dizziness, vomiting, nightmares, headache, and/or paresthesias (prickling, tingling sensation on the skin).

    Depression is also a part of bipolar illness. People with bipolar disorder who take antidepressants may be at risk for "switching" from depression into mania. Symptoms of mania include "high" or irritable mood, very high self-esteem, decreased need for sleep, pressure to keep talking, racing thoughts, being easily distracted, frequently involved in activities with a large risk for bad consequences (for example, excessive buying sprees).

    Medical attention should be sought if serotonin syndrome is suspected. Please refer to serious side effects for signs/symptoms.

    Are There Specific Concerns About Tranylcypromine And Pregnancy?
    If you are planning on becoming pregnant, notify your health care provider to best manage your medications. People living with MDD who wish to become pregnant face important decisions. Untreated MDD has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Regarding breastfeeding, caution is advised as tranylcypromine passes into breast milk. Further discusses should be discussed with health care provider.

    What Should I Discuss With My Health Care Provider Before Taking Tranylcypromine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, including a history of bipolar disorder
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breastfeeding
    If you drink alcohol or use drugs

    How Should I Take Tranylcypromine?
    Tranylcypromine is usually taken one to three times per day depending on dose with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 10mg to 60mg. Only your health care provider can determine the correct dose for you.

    Consider using a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Tranylcypromine?
    If you miss a dose of tranylcypromine take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your health care provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Tranylcypromine?
    Avoid drinking alcohol or using illegal drugs while you are taking antidepressant medications. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    Special dietary considerations: Foods rich in tyramine and may cause a sudden and severe high blood pressure (hypertensive crisis). Avoid high protein food that has undergone protein break down via aging, fermentation, pickling, smoking, or bacterial contamination. Also avoid beverages containing tyramine. Food freshness is also important; avoid any food that may potentially be spoiled, improperly refrigerated, stored, or handled. It is important to also avoid food with excessive amounts of caffeine and/or chocolate.

    Examples of food to avoid include:

    Dry sausage (salami, pepperoni)
    Cheeses (aged cheeses including parmesan, aged cheddar, bleu cheese)
    Beer, wine
    Pickled herring
    Liver
    Fava or broad bean pods
    Sauerkraut
    Avoid foods/beverages with excessive amounts of caffeine/chocolate

    These dietary considerations should be taken into consideration for 2 weeks even after tranylcypromine is discontinued. Discuss with health care provider any other foods or specific dietary concerns.

    What Happens If I Overdose With Tranylcypromine?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of tranylcypromine does not exist.

    What Are The Possible Side Effects Of Tranylcypromine?
    Common side effects

    Sedation
    Dry mouth
    Abdominal pain
    Lack of appetite
    Decreased blood pressure (hypotension)
    Heart palpitations, increased heart rate
    Constipation
    Sexual dysfunction
    Sweating
    Itching

    Rare side effects

    Elevated sodium levels
    Liver dysfunction
    Skin rash
    Seizures
    Hypertensive crisis; especially if low tyramine diet is not followed
    Serotonin Syndrome

    Hypertensive crisis (symptoms may include occipital headache-start in the back and radiate to the front, heart palpitations, nausea/vomiting, neck stiffness/soreness, light sensitivity, sweating)

    Serotonin syndrome (symptoms may include shivering, diarrhea, confusion, severe muscle tightness, fever, seizures, and death)

    Are There Any Risks For Taking Tranylcypromine For Long Periods Of Time?
    To date, there are no known problems associated with long term use of tranylcypromine. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Tranylcypromine?
    Tranylcypromine should not be taken with or within 2 weeks (5 weeks for fluoxetine) of any other mental health medications including other antidepressants, mood stabilizers, antipsychotics, and anti-anxiety medications. Tranylcypromine may also interact with some pain medication, medications for migraines, amphetamines, and antibiotics. Please inform your health care providers of all your current medications and any substance use at the time of prescribing to avoid any potential side effects.

    There is an increased risk of serotonin syndrome when tranylcypromine is used with other medications that increase serotonin, such as other antidepressants, migraine medications called “triptans” (e.g., Imitrex®), some pain medications (e.g., tramadol (Ultram®), amphetamines, and the antibiotic linezolid (Zyvox®).

    The following medications may increase the levels and effects of tranylcypromine: alcohol, alfuzosin, amantadine, antipsychotics, barbiturates, blood pressure lowering agents, buprenorphine, buspirone, carbamazepine, cyclobenzaprine, fentanyl, ipratropium (oral inhalation), levodopa, methadone, methylene blue, oxycodone, opioid analgesics, pentoxifylline, pheniramine, phosphodiesterase 5 inhibitors (including sildenafil), tramadol, tetrabenazine, valbenazine

    The following medications may decrease the levels and effects of tranylcypromine: acetylcholinesterase inhibitors, amifampridine, cyproheptadine, domperidone.

    Tranylcypromine may increase the levels and effects of antipsychotics, atomoxetine, bupropion, cyproheptadine, deutetrabenazine, dopamine, dextromethorphan, codeine, heroin, hydrocodone, lithium, methylphenidate, morphine, mirtazapine, MAO-Is, norepinephrine, opioid analgesics, pindolol, SSRIs, SNRIs, topiramate, tramadol, tricyclic antidepressants.

    Tranylcypromine may decrease the levels and effects of acetylcholinesterase inhibitors, gastrointestinal agents, amifampridine, domperidone, nitroglycerin, secretin.

    How Long Does It Take For Tranylcypromine To Work?
    Sleep, energy, or appetite may show some improvement within the first 1-2 weeks. Improvement in these physical symptoms can be an important early signal that the medication is working. Depressed mood and lack of interest in activities may need up to 6-8 weeks to fully improve.

    Summary Of FDA Black Box Warnings
    Suicidal thoughts or actions in children and adults

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide. Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking antidepressant medications. This risk may persist until significant remission occurs.

    In short-term studies, antidepressants increased the risk of suicidality in children, adolescents, and young adults when compared to placebo. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24. Adults age 65 and older taking antidepressants have a decreased risk of suicidality. Patients, their families, and caregivers should be alert to the emergence of anxiety, restlessness, irritability, aggressiveness and insomnia. If these symptoms emerge, they should be reported to the patient’s prescriber or health care professional. All patients being treated with antidepressants for any indication should watch for and notify their health care provider for worsening symptoms, suicidality and unusual changes in behavior, especially during the first few months of treatment.

  • Ingrezza (Valbenazine)

    Brand name: Ingrezza®

    Capsules: 40 mg and 80 mg
    Generic name: valbenazine (val BEN a zeen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Valbenazine And What Does It Treat?
    Valbenazine is a medication that is used to decrease the frequency and severity of involuntary, uncontrollable muscle movements that are related to a condition known as Tardive Dyskinesia (TD). TD is associated with chronic use of certain medications, such as antipsychotics.

    Symptoms of TD include:

    Lip smacking, puckering, or pursing
    Tongue rolling or darting in and out of mouth
    Jaw clenching or grimacing
    Trunk and hip rocking, jerking, or thrusting
    Twisting or rhythmic movement in fingers and toes
    Valbenazine may help improve some or all of these symptoms.

    What Is The Most Important Information I Should Know About Valbenazine?
    For valbenazine to work properly, it should be taken every day as prescribed by your healthcare provider.

    Missing doses of valbenazine may increase your risk for a relapse in your symptoms.

    Valbenazine may cause drowsiness. Avoid activities that require alertness, such as driving a car or operating machinery until you learn how your body respond to it.

    If you feel faint or have heart palpitations, consult with your doctor immediately.

    With input from you, your health care provider will assess how long you will need to take the medicine. Do not stop taking valbenazine or change your dose without talking to your healthcare provider first.

    Are There Specific Concerns About Valbenazine And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with TD who wish to become pregnant face important decisions. Currently, there are no well-controlled human studies of valbenazine in pregnancy. However, increased rates of stillbirths were seen in animal studies. It is important to discuss the risk and benefits of treatment with your doctor and caregivers.

    Caution is advised with breast-feeding since it is not known if valbenazine passes into your breast milk. However, increased rates of perinatal mortality were seen in animal studies. Therefore, the manufacturer recommends against breastfeeding during treatment with valbenazine and for 5 days after the last dose. Talk to your doctor about the best way to feed your baby during treatment with valbenazine.

    What Should I Discuss With My Healthcare Provider Before Taking Valbenazine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, such as depression, heart rhythm problems, long QT syndrome, heart attacks, kidney disease, or liver disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you drink alcohol or use illegal drugs


    How Should I Take Valbenazine?
    Valbenazine is usually taken once a day, with or without food.

    Typically patients begin at 40 mg once a day and dose may be increased to 80 mg once a day after a week of treatment. Only your healthcare provider can determine the correct dose for you.

    You will need to plan for a caregiver or family member to drive you home after each treatment.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Valbenazine?
    If you miss a dose of valbenazine, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Valbenazine?
    Avoid drinking alcohol or using illegal drugs while you are taking valbenazine. They may decrease the benefits (e.g. worsen your condition) and increase adverse effects (e.g. sedation) of the medication.

    What Happens If I Overdose With Valbenazine?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific antidote to reverse the effects of valbenazine does not exist.

    What Are Possible Side Effects Of Valbenzine?
    Common side effects

    The most common side effects of taking valbenazine are fatigue, drowsiness, and sleepiness.

    Rare/serious side effects

    Rare/serious side effects may include headache, nausea, vomiting, dizziness, muscle aches, increases in weight or blood sugar, restlessness, abnormal muscle movements, irregular heart rhythm, rash, and swelling of the face, lips, and mouth.

    Are There Any Risks For Taking Valbenazine For Long Periods Of Time?
    To date, there are no known problems associated with long term use of valbenazine. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Valbenazine?
    Valbenazine should not be taken with or within 2 weeks of taking monoamine oxidase inhibitors (MAOIs), as these medications can increase side effects and decrease the effectiveness of valbenazine. MAOIs include phenelzine (Nardil®), tranylcypromine (Parnate®), isocarboxazid (Marplan®), and selegiline (Emsam®).

    The following medications may increase the levels and effects of valbenazine:

    The antidepressants paroxetine (Paxil®) and fluoxetine (Prozac®)
    Antifungal medications itraconazole (Sporanox®) and ketoconazole (Nizoral®) and antibiotics like clarithromycin (Biaxin®)
    The following medications may decrease the levels and effects of valbenazine:

    Certain seizure medications, such as carbamazepine (Tegretol®) or phenytoin (Dilantin®)
    The antibiotic rifampin (Rifadin®)
    Herbal supplements containing St. John’s wort
    Concurrent use of valbenazine may increase the level of antiarrhythmic medication digoxin (Lanoxin®)

    Using valbenazine with antipsychotics, tricyclic antidepressants, certain heart medications and antibiotics may increase the risk of developing irregular heart rhythms.

    How Long Does It Take For Valbenazine To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking valbenazine. It may take several weeks to see big enough changes in your symptoms to decide if valbenazine is the right medication for you.

    Summary Of FDA Black Box Warnings
    No black box warnings exist for this medication at this time.

  • Depakote (Valproate )

    Brand names:

    Depakene®Capsule (immediate release): 250 mg
    ​Oral solution: 250 mg/5mL
    Depakote®Tablet (delayed release): 125 mg, 250 mg, 500 mg
    Sprinkle capsule (delayed release): 125 mg
    Depakote ER®Tablet (extended release): 250 mg, 500 mg
    Stavzor®Capsule (delayed release): 125 mg, 250 mg, 500mp
    Generic names:

    Valproate (val PROE ate)
    Divalproex (dye val PRO ex) sodium
    Valproic (val PROE ik) acid
    Note: Throughout this fact sheet, the medication will be referred to as valproate. Even though valproate is available in different names, strengths, and formulations, all provide the same active medicine.

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Valproate And What Does It Treat?
    Valproate is a mood stabilizer medication that works in the brain. It is approved for the treatment of mania associated with bipolar disorder (also known as manic depression), seizures (epilepsy), and migraine headaches. Bipolar disorder involves episodes of depression and/or mania.

    Symptoms of depression include:

    Depressed mood — feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, or helpless
    Loss of interest or pleasure in normal activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving in slow motion)
    Symptoms of mania include:

    Feeling irritable or “high”
    Having increased self esteem
    Feeling like you don’t need to sleep
    Feeling the need to continue to talk
    Feeling like your thoughts are too quick (racing thoughts)
    Feeling distracted
    Getting involved in activities that are risky or could have bad consequences (e.g. excessive spending)
    Valproate may also be helpful when prescribed “off-label” for diabetic peripheral neuropathy, postherpetic neuralgia, status epilepticus, and some conditions related to a traumatic brain injury (agitation, aggression, and seizure prevention). “Off-label” means that it hasn’t been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an “off-label” treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Valproate?
    Bipolar disorder requires long-term treatment. Do not stop taking valproate, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine. Missing doses of valproate may increase your risk for a relapse in your mood symptoms.

    Do not stop taking valproate or change your dose without talking to your healthcare provider first.

    In order for valproate to work properly, it should be taken every day as ordered by your healthcare provider.

    Periodically, your healthcare provider may ask you to provide a blood sample to make sure the appropriate level of medication is in your body and to assess for side effects, such as changes in blood cell counts.

    Are There Specific Concerns About Valproate And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider so that he/she can best manage your medications. People living with bipolar disorder who wish to become pregnant face important decisions. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Valproate has been associated with an increased risk of spinal cord defects (spina bifida). Bleeding, liver problems, decreased IQ scores, developmental delays, and other birth defects have also been reported. There may be precautions to decrease the risk of these effects. Discontinuing mood stabilizer medications during pregnancy has been associated with a significant increase in symptom relapse.

    Regarding breast-feeding, caution is advised since valproate does pass into breast milk in small amounts.

    What Should I Discuss With My Healthcare Provider Before Taking Valproate?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you drink alcohol or use illegal drugs


    How Should I Take Valproate?
    Valproate is usually is taken 1-3 times daily with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 1000 mg to 3500 mg or more. Only your healthcare provider can determine the correct dose for you, as sometimes the dose required is based on your weight.

    Valproate tablets: Swallow whole. Do not crush, chew or split tablets.

    Depakote Sprinkle® capsules: Swallow whole or sprinkle onto food, such as applesauce or pudding and eat immediately. Do not chew the sprinkle capsule or contents.

    Valproate syrup: Measure with a dosing spoon or oral syringe that you can get from your pharmacy.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Valproate?
    If you miss a dose of valproate, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your dose or take more than what is prescribed.

    What Should I Avoid While Taking Valproate?
    Avoid drinking alcohol or using illegal drugs while you are taking valproate. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Valproate?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of valproate does not exist.

    What Are Possible Side Effects Of Valproate?
    Common side effects

    Nausea or vomiting
    Headache
    Drowsiness or dizziness
    Tremor
    Muscle weakness
    Insomnia
    Hair loss
    Weight gain
    Diarrhea or abdominal pain


    Rare/serious side effects

    Liver problems
    Low platelets. Platelets help the blood to clot. Bruising easier than normal is a symptom of low platelets
    Pancreatitis (inflammation of the pancreas). Symptoms of pancreatitis include severe stomach pain, nausea, vomiting, and not feeling hungry
    Increased ammonia levels. If this happens, you may get confused, disoriented, or have difficulty thinking.
    Studies have found that individuals who take antiepileptic medications including valproate have suicidal thoughts or behaviors up to twice as often than individuals who take placebo (inactive medication). These thoughts or behaviors occurred in approximately 1 in 500 patients taking the antiepileptic class of medications. If you experience any thoughts or impulses to hurt yourself, you should contact your doctor immediately.

    Are There Any Risks For Taking Valproate For Long Periods Of Time?
    To date, there are no known problems associated with long term use of valproate. It is a safe and effective medication when used as directed.

    It is important to note that some of the side effects listed above (particularly changes in platelets, liver or pancreas problems, and suicidal thoughts) may continue to occur or worsen if you continue taking the medication. It is important to follow up with your doctor for blood work and to contact your doctor immediately if you notice abdominal pain, sudden nausea or vomiting, or changes in mood or behavior.

    What Other Medications May Interact With Valproate?
    Combining valproate with topiramate (Topamax®) may increase ammonia levels in your blood. If this happens, you may get confused, disoriented, or have difficulty thinking.

    The following medications may increase the level and effects of valproate:

    Aspirin (high doses to treat fever or pain)
    The following medications may decrease the level and effect of valproate:

    Anticonvulsant medications such as phenytoin (Dilantin®), carbamazepine (Tegretol®/Carbatrol®/Equetro®), and phenobarbital
    Rifampin (Rifadin®)
    Certain antibiotics, such as ertapenem (Invanz®) or meropenem (Merrem®)
    Valproate may increase the level and effects of:

    Antidepressant medications such as amitriptyline (Elavil®) and nortriptyline (Pamelor®)
    Anticonvulsant medications such as phenytoin (Dilantin®), carbamazepine (Tegretol®/Carbatrol®/Equetro®), rufinamide (Banzel®), ethosuxamide (Zarontin®), and especially lamotrigine (Lamictal®).
    Diazepam (Valium®)
    Valproate may decrease the level and effects of:

    Olanzapine (Zyprexa®)
    Oxcarbazepine (Trileptal®)
    How Long Does It Take For Valproate To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking valproate. It will probably take several weeks to see big enough changes in your symptoms to decide if valproate is the right medication for you.

    Mood stabilizer treatment is generally needed lifelong for persons with bipolar disorder. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Summary Of FDA Black Box Warnings
    Liver Damage

    Serious and fatal liver damage has been associated with valproate, particularly during the first six months of treatment.

    Mitochondrial Disease

    Patients with mitochondrial disease caused by a certain DNA mutation are at an increased risk of acute liver failure and resultant death.

    Birth Defects

    Birth defects have been found in babies born to mothers who took valproate while pregnant.

    Pancreatitis

    Life threatening pancreatitis has been reported in children and adults who take valproate. Signs of pancreatitis include severe abdominal pain, nausea, vomiting and inability to keep food down.

  • Effexor (Venlafaxine)

    Brand names:

    Effexor®Tablets (immediate release): 25 mg, 37.5 mg, 50 mg, 75 mg, 100 mg
    Effexor XR®Capsules (extended release): 37.5 mg, 75 mg, 150 mg
    VenlafaxineTablets (extended release): 37.5, 75 mg, 150 mg, 225 mg
    Tablets (immediate release): 25 mg, 37.5 mg, 50 mg 75, mg 100 mg

    Generic name: venlafaxine (ven la FAX een)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Venlafaxine And What Does It Treat?
    Venlafaxine is an antidepressant medication that works in the brain. It is approved for the treatment of major depressive disorder (MDD), generalized anxiety disorder (GAD), panic disorder, and social anxiety disorder (social phobia).

    Symptoms of depression include:

    Depressed mood - feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, and helpless
    Loss of interest or pleasure in your usual activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving and thinking in slow motion)
    Suicidal thoughts or behaviors

    Generalized Anxiety Disorder (GAD) occurs when a person experiences excessive anxiety or worry for at least six months. Other symptoms include:

    Restlessness
    Fatigue (low energy, feeling tired all the time)
    Difficulty concentrating
    Irritability
    Muscle tension
    Sleep disturbance (difficulty falling asleep or waking up in the middle of the night)

    Panic Disorder occurs when a person experiences unexpected and repeated episodes of intense fear. These episodes have physical symptoms including chest pain, shortness of breath, heart palpitations, sweating, dizziness, and nausea. Fear of future episodes is also part of panic disorder.

    Social phobia/social anxiety disorder is a fear of situations where one may feel as if they are being judged by others. Symptoms include:

    Blushing
    Difficulty talking
    Nausea
    Sweating
    Shaking

    Venlafaxine may also be helpful when prescribed “off-label” for attention-deficit/hyperactivity disorder (ADHD) in adults and children/adolescents, diabetic neuropathy, migraine prevention, hot flashes, obsessive compulsive disorder (OCD), posttraumatic stress disorder (PTSD), and premenstrual dysphoric disorder (PMDD) . “Off-label” means that it hasn't been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending any “off-label” treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Venlafaxine?
    Do not stop taking venlafaxine, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of venlafaxine may increase your risk for relapse in your symptoms.

    Stopping venlafaxine abruptly may result in one or more of the following withdrawal symptoms: irritability, nausea, feeling dizzy, vomiting, nightmares, headache, and/or paresthesias (prickling, tingling sensation on the skin).

    Depression is also a part of bipolar illness. People with bipolar disorder who take antidepressants may be at risk for "switching" from depression into mania. Symptoms of mania include "high" or irritable mood, very high self-esteem, decreased need for sleep, pressure to keep talking, racing thoughts, being easily distracted, frequently involved in activities with a large risk for bad consequences (for example, excessive buying sprees).

    Medical attention should be sought if serotonin syndrome is suspected. Please refer to serious side effects for signs/symptoms.

    Are There Specific Concerns About Venlafaxine And Pregnancy?
    If you are planning on becoming pregnant, notify your health care provider to best manage your medications. People living with MDD who wish to become pregnant face important decisions. Untreated MDD has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers. For women who take antidepressant medications during weeks 13 through the end of their pregnancy (second and third trimesters), there is a risk that the baby can be born before it is fully developed (before 37 weeks).

    Caution is advised with breastfeeding since venlafaxine does pass into breast milk.

    What Should I Discuss With My Health Care Provider Before Taking Venlafaxine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, including a history of bipolar disorder
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breastfeeding
    If you drink alcohol or use drugs

    How Should I Take Venlafaxine?
    Venlafaxine immediate release tablets are usually taken two or three times per day with or without food. The extended release tablets and capsules are taken one time per day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 37.5 mg to 300 mg. Only your health care provider can determine the correct dose for you.

    Extended release tablets: swallow whole; do not chew, crush, or break

    Extended release capsules: swallow whole or sprinkle onto food, such as applesauce or pudding and eat immediately.

    Consider using a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Venlafaxine?
    If you miss a dose of venlafaxine, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your health care provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Venlafaxine?
    Avoid drinking alcohol or using illegal drugs while you are taking antidepressant medications. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Venlafaxine?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of venlafaxine does not exist.

    What Are The Possible Side Effects Of Venlafaxine?
    Common side effects

    Headache, nausea, diarrhea, dry mouth, increased sweating
    Feeling nervous, restless, fatigued, sleepy or having trouble sleeping (insomnia)
    These will often improve over the first week or two as you continue to take the medication.

    Sexual side effects, such as problems with orgasm or ejaculatory delay
    Increased blood pressure
    These often do not improve over time.

    Rare/serious side effects

    Increased heart rate, low blood pressure, increased salivation, irregular menstrual cycle, increased frequency of urination, changes in taste, low sodium (symptoms of low sodium levels may include headache, weakness, difficulty concentrating and remembering), teeth grinding, difficulty urinating, angle closure glaucoma (symptoms of angle closure glaucoma may include eye pain, changes in vision, swelling or redness in or around eye).

    Serotonin syndrome (symptoms may include shivering, diarrhea, confusion, severe muscle tightness, fever, seizures, and death)

    SNRI antidepressants including venlafaxine may increase the risk of bleeding events. Combined use of aspirin, nonsteroidal anti-inflammatory drugs (e.g., ibuprofen, naproxen), warfarin, and other anti-coagulants may increase this risk. This may include gums that bleed more easily, nose bleed, or gastrointestinal bleeding. Some cases have been life threatening.

    Are There Any Risks For Taking Venlafaxine For Long Periods Of Time?
    To date, there are no known problems associated with long term use of venlafaxine. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Venlafaxine?
    Venlafaxine should not be taken with or within 2 weeks of taking monoamine oxidase inhibitors (MAOIs). These include phenelzine (Nardil®), tranylcypromine (Parnate®), isocarboxazid (Marplan®), rasagiline (Azilect®), and selegiline (Emsam®).

    Although rare, there is an increased risk of serotonin syndrome when venlafaxine is used with other medications that increase serotonin, such as other antidepressants, migraine medications called “triptans” (e.g., Imitrex®), some pain medications (e.g., tramadol (Ultram®), and the antibiotic linezolid (Zyvox®).

    Venlafaxine may increase the effects of other medications that can cause bleeding (e.g., ibuprofen (Advil®, Motrin®), warfarin (Coumadin®) and aspirin).

    How Long Does It Take For Venlafaxine To Work?
    Sleep, energy, or appetite may show some improvement within the first 1-2 weeks. Improvement in these physical symptoms can be an important early signal that the medication is working. Depressed mood and lack of interest in activities may need up to 6-8 weeks to fully improve.

    Summary Of FDA Black Box Warnings
    Suicidal thoughts or actions in children and adults

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide. Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking antidepressant medications. This risk may persist until significant remission occurs.

    In short-term studies, antidepressants increased the risk of suicidality in children, adolescents, and young adults when compared to placebo. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24. Adults age 65 and older taking antidepressants have a decreased risk of suicidality. Patients, their families, and caregivers should be alert to the emergence of anxiety, restlessness, irritability, aggressiveness and insomnia. If these symptoms emerge, they should be reported to the patient’s prescriber or health care professional. All patients being treated with antidepressants for any indication should watch for and notify their health care provider for worsening symptoms, suicidality and unusual changes in behavior, especially during the first few months of treatment.

  • Viibryd (Vilazodone)

    Brand name: Viibryd®

    Tablets: 10 mg, 20 mg, 40 mg

    Generic name: vilazodone (vil AZ oh done)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Vilazodone And What Does It Treat?
    Vilazodone is an antidepressant medication that works in the brain. It is approved for the treatment of major depressive disorder (MDD).

    Symptoms of depression include:

    Depressed mood - feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, and helpless
    Loss of interest or pleasure in your usual activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving and thinking in slow motion)
    Suicidal thoughts or behaviors

    What Is The Most Important Information I Should Know About Vilazodone?
    Do not stop taking vilazodone, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of vilazodone may increase your risk for relapse in your symptoms.

    Stopping vilazodone abruptly may result in one or more of the following withdrawal symptoms: irritability, nausea, feeling dizzy, vomiting, nightmares, headache, and/or paresthesias (prickling, tingling sensation on the skin).

    Depression is also a part of bipolar illness. People with bipolar disorder who take antidepressants may be at risk for "switching" from depression into mania. Symptoms of mania include "high" or irritable mood, very high self-esteem, decreased need for sleep, pressure to keep talking, racing thoughts, being easily distracted, frequently involved in activities with a large risk for bad consequences (for example, excessive buying sprees).

    Medical attention should be sought if serotonin syndrome is suspected. Please refer to serious side effects for signs/symptoms.

    Are There Specific Concerns About Vilazodone And Pregnancy?
    If you are planning on becoming pregnant, notify your health care provider to best manage your medications. People living with MDD who wish to become pregnant face important decisions. Untreated MDD has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Caution is advised with breastfeeding since vilazodone does pass into breast milk.

    What Should I Discuss With My Health Care Provider Before Taking Vilazodone?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, including a history of bipolar disorder
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breastfeeding
    If you drink alcohol or use drugs

    How Should I Take Vilazodone?
    Vilazodone is usually taken one time per day with food or milk.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 20 mg to 40 mg. Only your health care provider can determine the correct dose for you.

    Consider using a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Vilazodone?
    If you miss a dose of vilazodone, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your health care provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Vilazodone?
    Avoid drinking alcohol or using illegal drugs while you are taking antidepressant medications. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Vilazodone?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of vilazodone does not exist.

    What Are The Possible Side Effects Of Vilazodone?
    Common side effects

    Diarrhea, nausea, vomiting, dry mouth, dizziness, insomnia
    Rare/serious side effects

    Night sweats, decreased appetite, migraine headaches, sleepiness, tremor, blurry vision, dry eyes, abnormal dreams, agitation, restlessness, increased urination, sexual dysfunction, angle closure glaucoma (symptoms of angle closure glaucoma may include eye pain, changes in vision, swelling or redness in or around eye), Serotonin syndrome (symptoms may include shivering, diarrhea, confusion, severe muscle tightness, fever, seizures, and death), palpitations, irregular heartbeat

    Vilazodone may increase the risk of bleeding events. Combined use of aspirin, nonsteroidal anti-inflammatory drugs (e.g., ibuprofen, naproxen), warfarin, and other anti-coagulants may increase this risk. This may include gums that bleed more easily, nose bleed, or gastrointestinal bleeding. Some cases have been life threatening.

    Are There Any Risks For Taking Vilazodone For Long Periods Of Time?
    To date, there are no known problems associated with long term use of vilazodone. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Vilazodone?
    Vilazodone should not be taken with or within 2 weeks of taking monoamine oxidase inhibitors (MAOIs). These include phenelzine (Nardil®), tranylcypromine (Parnate®), isocarboxazid (Marplan®), rasagiline (Azalect®) and selegiline (Emsam®).

    Although rare, there is an increased risk of serotonin syndrome when vilazodone is used with other medications that increase serotonin, such as other antidepressants, migraine medications called “triptans” (e.g., Imitrex®), some pain medications (e.g., tramadol (Ultram®), and the antibiotic linezolid (Zyvox®).

    The following medications may increase the levels and effects of vilazodone requiring decreased dose of vilazodone:

    Antibiotics, such as clarithromycin (Biaxin®), erythromycin (Ery-Tab®), and telithromycin (Ketek®)
    Antifungals, such as fluconazole (Diflucan®), ketoconazole (Nizoral®), and itraconazole (Sporanox®)
    Blood pressure medications, such as verapamil (Calan®, Covera-HS®, Isoptin SR®) and diltiazem (Cardizem®, Tiazac®)
    HIV medications such as protease inhibitors: indinavir (Crixivan®), ritonavir (Norvir®), saquinavir (Fortovase®, Invirase®), and lopinavir/ritonavir (Kaletra®)
    Nefazodone
    The following medications may decrease the levels and effects of vilazodone requiring increased dose of vilazodone: carbamazepine (Tegretol®), oxcarbazepine (Trileptal®), rifampin (Rifadin®), phenytoin (Dilantin®), and phenobarbital

    How Long Does It Take For Vilazodone To Work?
    Sleep, energy, or appetite may show some improvement within the first 1-2 weeks. Improvement in these physical symptoms can be an important early signal that the medication is working. Depressed mood and lack of interest in activities may need up to 6-8 weeks to fully improve.

    Summary Of FDA Black Box Warnings
    Suicidal thoughts or actions in children and adults

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide. Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking antidepressant medications. This risk may persist until significant remission occurs.

    risk may persist until significant remission occurs.
    In short-term studies, antidepressants increased the risk of suicidality in children, adolescents, and young adults when compared to placebo. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24. Adults age 65 and older taking antidepressants have a decreased risk of suicidality. Patients, their families, and caregivers should be alert to the emergence of anxiety, restlessness, irritability, aggressiveness and insomnia. If these symptoms emerge, they should be reported to the patient’s prescriber or health care professional. All patients being treated with antidepressants for any indication should watch for and notify their health care provider for worsening symptoms, suicidality and unusual changes in behavior, especially during the first few months of treatment.

  • Geodon (Ziprasidone)

    Brand name:​ Geodon®

    Capsule: 20 mg, 40 mg, 60 mg, 80 mg
    Injection (immediate release): 20 mg/mL
    Generic name: ziprasidone (zi PRAS i done)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Ziprasidone And What Does It Treat?
    Ziprasidone is a medication that works in the brain to treat schizophrenia. It is also known as a second generation antipsychotic (SGA) or atypical antipsychotic. Ziprasidone rebalances dopamine and serotonin to improve thinking, mood, and behavior.

    Symptoms of schizophrenia include:

    Hallucinations — imagined voices or images that seem real
    Delusions — beliefs that are not true (e.g., other people are reading your thoughts)
    Disorganized thinking or trouble organizing your thoughts and making sense
    Little desire to be around other people
    Trouble speaking clearly
    Lack of motivation
    Ziprasidone may help some or all of these symptoms.

    Ziprasidone is also FDA approved for the following indications:

    Acute treatment of manic or mixed episodes of bipolar disorder
    Maintenance (long-term) treatment of bipolar disorder (when used with lithium or valproate)
    Acute treatment of agitation in schizophrenia
    This medication sheet will focus primarily on schizophrenia. You can find more information about bipolar disorder here.

    Ziprasidone may also be helpful when prescribed “off-label” for schizoaffective disorder. “Off-label” means that it hasn’t been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an “off-label” treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Ziprasidone?
    Schizophrenia requires long-term treatment. Do not stop taking ziprasidone, even when you feel better.

    With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of ziprasidone may increase your risk for a relapse in your symptoms.

    Do not stop taking ziprasidone or change your dose without talking with your healthcare provider first.

    For ziprasidone to work properly, it should be taken every day as ordered by your healthcare provider.

    Are There Specific Concerns About Ziprasidone And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with schizophrenia who wish to become pregnant face important decisions. This is a complex decision since untreated schizophrenia has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Antipsychotic use during the third trimester of pregnancy has a risk for abnormal muscle movements (extrapyramidal symptoms [EPS]) and/or withdrawal symptoms in newborns following delivery. Symptoms in the newborn may include agitation, feeding disorder, hypertonia, hypotonia, respiratory distress, somnolence, and tremor; these effects may be self-limiting or require hospitalization.

    Caution is advised with breastfeeding since ziprasidone does pass into breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Ziprasidone?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you ever had muscle stiffness, shaking, tardive dyskinesia, neuroleptic malignant syndrome, or weight gain caused by a medication
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any psychiatric or medical problems you have, such as heart rhythm problems, long QT syndrome, heart attacks, diabetes, high cholesterol, or seizures
    If you have a family history of diabetes or heart disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you smoke, drink alcohol, or use illegal drugs


    How Should I Take Ziprasidone?
    Ziprasidone is usually taken 2 times per day with food (at least 500 calories).

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 40 to 80 mg twice daily. Only your healthcare provider can determine the correct dose for you.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Ziprasidone?
    If you miss a dose of ziprasidone, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Ziprasidone?
    Avoid drinking alcohol or using illegal drugs while you are taking ziprasidone. They may decrease the benefits (e.g. worsen your confusion) and increase adverse effects (e.g. sedation) of the medication.

    What Happens If I Overdose With Ziprasidone?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of ziprasidone does not exist.

    What Are Possible Side Effects Of Ziprasidone?
    Common side effects

    Drowsiness, extrapyramidal symptoms, headache, dizziness, nausea

    Rare/serious side effects

    Ziprasidone may increase the blood levels of a hormone called prolactin. Side effects of increased prolactin levels include females losing their period, production of breast milk and males losing their sex drive or possibly experiencing erectile problems. Long term (months or years) of elevated prolactin can lead to osteoporosis, or increased risk of bone fractures.

    Some people may develop muscle related side effects while taking ziprasidone. The technical terms for these are “extrapyramidal symptoms” (EPS) and “tardive dyskinesia” (TD). Symptoms of EPS include restlessness, tremor, and stiffness. TD symptoms include slow or jerky movements that one cannot control, often starting in the mouth with tongue rolling or chewing movements.

    Temperature regulation: Impaired core body temperature regulation may occur; caution with strenuous exercise, heat exposure, and dehydration.

    Second generation antipsychotics (SGAs) increase the risk of weight gain, high blood sugar, and high cholesterol. This is also known as metabolic syndrome. Your healthcare provider may ask you for a blood sample to check your cholesterol, blood sugar, and hemoglobin A1c (a measure of blood sugar over time) while you take this medication.

    Information on healthy eating and adding exercise to decrease your chances of developing metabolic syndrome may be found at the following sites:

    http://www.helpguide.org/articles/healthy-eating/healthy-eating.htm
    http://www.helpguide.org/home-pages/exercise-fitness.htm
    SGAs have been linked with higher risk of death, strokes, and transient ischemic attacks (TIAs) in elderly people with behavior problems due to dementia.

    All antipsychotics have been associated with the risk of sudden cardiac death due to an arrhythmia (irregular heartbeat). To minimize this risk, antipsychotic medications should be used in the smallest effective dose when the benefits outweigh the risks. Your doctor may order an EKG to monitor for irregular heartbeat.

    Neuroleptic malignant syndrome is a rare, life threatening adverse effect of antipsychotics which occurs in

    All antipsychotics can cause sedation, dizziness, or orthostatic hypotension (a drop in blood pressure when standing up from sitting or lying down). These side effects may lead to falls which could cause bone fractures or other injuries. This risk is higher for people with conditions or other medications that could worsen these effects. If falls or any of these symptoms occur, contact your healthcare provider.

    Severe skin reactions have been reported with ziprasidone. These include Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) and Stevens-Johnson Syndrome which can be fatal. Seek emergency treatment immediately if a severe skin reaction occurs.

    Are There Any Risks For Taking Ziprasidone For Long Periods Of Time?
    Tardive dyskinesia (TD) is a side effect that develops with prolonged use of antipsychotics. Medications such as ziprasidone have been shown to have a lower risk of TD compared to older antipsychotics, such as Haldol® (haloperidol). If you develop symptoms of TD, such as grimacing, sucking, and smacking of lips, or other movements that you cannot control, contact your healthcare provider immediately. All patients taking either first or second generation antipsychotics should have an Abnormal Involuntary Movement Scale (AIMS) completed regularly by their healthcare provider to monitor for TD.

    Second generation antipsychotics (SGAs) increase the risk of diabetes, weight gain, high cholesterol, and high triglycerides. (See “Serious Side Effects” section for monitoring recommendations).

    What Other Medications May Interact With Ziprasidone?
    Ziprasidone may block the effects of agents used to treat Parkinson’s disease such as levodopa/carbidopa (Sinemet®), bromocriptine, pramipexole (Mirapex®), ropinirole (Requip®), and others.

    The following medications may increase the risk of heart problems when used with ziprasidone:

    Antipsychotics, including chlorpromazine (Thorazine®), thioridizine (Mellaril®), asenapine (Saphris®), iloperidone (Fanapt®), paliperidone (Invega®), and quetiapine (Seroquel®)
    Antiarrhythmics (heart rhythm medications), including procainamide, quinidine, amiodarone (Cordarone®), dronedarone (Multaq®), and sotalol (Betapace®)
    The following medications may increase the levels and effects of ziprasidone: fluoxetine (Prozac®), ketoconazole (Nizoral®), and paroxetine (Paxil®).

    Carbamazepine (Tegretol®) may decrease the levels and effects of ziprasidone.

    How Long Does It Take For Ziprasidone To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking ziprasidone. It will probably take several weeks to see big enough changes in your symptoms to decide if ziprasidone is the right medication for you.

    Antipsychotic treatment is generally needed lifelong for persons with schizophrenia. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Hallucinations, disorganized thinking, and delusions may improve in the first 1-2 weeks
    Sometimes these symptoms do not completely go away
    Motivation and desire to be around other people can take at least 1-2 weeks to improve
    Symptoms continue to get better the longer you take ziprasidone
    It may take 2-3 months before you get the full benefit of ziprasidone


    Summary Of FDA Black Box Warnings
    Increased mortality in elderly patients with dementia-related psychosis

    Both first generation (typical) and second generation (atypical) antipsychotics are associated with an increased risk of mortality in elderly patients when used for dementia related psychosis.
    Although there were multiple causes of death in studies, most deaths appeared to be due to cardiovascular causes (e.g. sudden cardiac death) or infection (e.g. pneumonia).
    Antipsychotics are not indicated for the treatment of dementia-related psychosis.

  • Trintellix (Vortioxetine)

    Brand name: Trintellix®

    Tablets: 5 mg, 10 mg, 20 mg

    Generic name: vortioxetine (vor tye OX e teen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Vortioxetine And What Does It Treat?
    Vortioxetine is an antidepressant medication that works in the brain. It is approved for the treatment of major depressive disorder (MDD).

    Symptoms of depression include:

    Depressed mood - feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, and helpless
    Loss of interest or pleasure in your usual activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving and thinking in slow motion)
    Suicidal thoughts or behaviors

    What Is The Most Important Information I Should Know About Vortioxetine?
    Do not stop taking vortioxetine, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of vortioxetine may increase your risk for relapse in your symptoms.

    Stopping vortioxetine abruptly may result in one or more of the following withdrawal symptoms: irritability, nausea, dizziness, vomiting, nightmares, headache, and/or paresthesias (prickling, tingling sensation on the skin).

    Depression is also a part of bipolar illness. People with bipolar disorder who take antidepressants may be at risk for "switching" from depression into mania. Symptoms of mania include "high" or irritable mood, very high self-esteem, decreased need for sleep, pressure to keep talking, racing thoughts, being easily distracted, frequently involved in activities with a large risk for bad consequences (for example, excessive buying sprees).

    Medical attention should be sought if serotonin syndrome is suspected. Please refer to serious side effects for signs/symptoms.

    Are There Specific Concerns About Vortioxetine And Pregnancy?
    If you are planning on becoming pregnant, notify your health care provider to best manage your medications. People living with MDD who wish to become pregnant face important decisions. Untreated MDD has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    For mothers who have taken SSRIs during their pregnancy, there appears to be less than a 1% chance of infants developing persistent pulmonary hypertension. This is a potentially fatal condition that is associated with use of the antidepressant in the second half of pregnancy. However, women who discontinued antidepressant therapy were five times more likely to have a depression relapse than those who continued their antidepressant. If you are pregnant, please discuss the risks and benefits of antidepressant use with your health care provider.

    Regarding breastfeeding, caution is advised since it is not known if vortioxetine passes into breast milk.

    What Should I Discuss With My Health Care Provider Before Taking Vortioxetine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, including a history of bipolar disorder
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breastfeeding
    If you drink alcohol or use drugs

    How Should I Take Vortioxetine?
    Vortioxetine is usually taken one time per day without regard to meals.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 5 mg to 20 mg. Only your health care provider can determine the correct dose for you.

    Consider using a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Vortioxetine?
    If you miss a dose of vortioxetine, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your health care provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Vortioxetine?
    Avoid drinking alcohol or using illegal drugs while you are taking antidepressant medications. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Vortioxetine?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of vortioxetine does not exist.

    What Are The Possible Side Effects Of Vortioxetine?
    Common side effects

    Nausea, constipation, vomiting, sexual dysfunction, dizziness, diarrheaRare/serious side effects

    Low sodium blood levels (symptoms of low sodium levels may include headache, weakness, difficulty concentrating and remembering), teeth grinding, angle closure glaucoma (symptoms of angle closure glaucoma may include eye pain, changes in vision, swelling or redness in or around eye), Serotonin syndrome (symptoms may include shivering, diarrhea, confusion, severe muscle tightness, fever, seizures, and death), seizure

    SSRI antidepressants including sertraline may increase the risk of bleeding events. Combined use of aspirin, nonsteroidal anti-inflammatory drugs (e.g., ibuprofen, naproxen), warfarin, and other anti-coagulants may increase this risk. This may include gums that bleed more easily, nose bleed, or gastrointestinal bleeding. Some cases have been life threatening.

    Are There Any Risks For Taking Vortioxetine For Long Periods Of Time?
    To date, there are no known problems associated with long term use of vortioxetine. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Vortioxetine?
    Vortioxetine should not be taken with or within 2 weeks of taking monoamine oxidase inhibitors (MAOIs). These include phenelzine (Nardil®), tranylcypromine (Parnate®), isocarboxazid (Marplan®), and selegiline (Emsam®).

    Although rare, there is an increased risk of serotonin syndrome when vortioxetine is used with other medications that increase serotonin, such as other antidepressants, migraine medications called “triptans” (e.g., Imitrex®), some pain medications (e.g., tramadol (Ultram®), and the antibiotic linezolid (Zyvox®).

    Vortioxetine may increase the effects of other medications that can cause bleeding (e.g., ibuprofen (Advil®, Motrin®), warfarin (Coumadin®) and aspirin)

    The following medications may increase the levels and effects of vortioxetine: bupropion (Wellbutrin®), fluoxetine (Prozac®), paroxetine (Paxil®), quinidine.

    The following medications may decrease the levels and effects of vortioxetine: rifampin (Rifadin®), carbamazepine (Tegretol®), phenytoin (Dilantin®).

    How Long Does It Take For Vortioxetine To Work?
    Sleep, energy, or appetite may show some improvement within the first 1-2 weeks. Improvement in these physical symptoms can be an important early signal that the medication is working. Depressed mood and lack of interest in activities may need up to 6-8 weeks to fully improve.

    Summary Of FDA Black Box Warnings
    Suicidal thoughts or actions in children and adults

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide. Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking antidepressant medications. This risk may persist until significant remission occurs.

    In short-term studies, antidepressants increased the risk of suicidality in children, adolescents, and young adults when compared to placebo. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24. Adults age 65 and older taking antidepressants have a decreased risk of suicidality. Patients, their families, and caregivers should be alert to the emergence of anxiety, restlessness, irritability, aggressiveness and insomnia. If these symptoms emerge, they should be reported to the patient’s prescriber or health care professional. All patients being treated with antidepressants for any indication should watch for and notify their health care provider for worsening symptoms, suicidality and unusual changes in behavior, especially during the first few months of treatment.

  • Clozaril and FazaClo (Clozapine)

    Brand names:

    Clozaril®Tablet: 25 mg, 50 mg, 100 mg, 200 mg
    FazaClo®Orally disintegrating tablet: 12.5 mg, 25 mg, 100 mg, 150 mg, 200 mg
    Versacloz®Oral suspension: 50 mg/mL
    Generic name: clozapine (KLOE za peen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Clozapine And What Does It Treat?
    Clozapine is a medication that works in the brain to treat schizophrenia. It is also known as a second generation antipsychotic (SGA) or atypical antipsychotic. Clozapine rebalances dopamine and serotonin to improve thinking, mood, and behavior.

    Symptoms of schizophrenia include:

    Hallucinations — imagined voices or images that seem real
    Delusions — beliefs that are not true (e.g., other people are reading your thoughts)
    Disorganized thinking or trouble organizing your thoughts and making sense
    Little desire to be around other people
    Trouble speaking clearly
    Lack of motivation
    Clozapine may help some or all of these symptoms.

    Clozapine is also FDA approved to reduce the risk of recurrent suicidal behavior in people with schizophrenia or schizoaffective disorder.

    Clozapine may also be helpful when prescribed "off-label" for patients with Parkinson's disease who have psychosis symptoms. Psychosis symptoms may include hallucinations and delusions. "Off-label" means that it hasn't been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an "off-label" treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Clozapine?
    Schizophrenia requires long-term treatment. Do not stop taking clozapine, even when you feel better.

    With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of clozapine may increase your risk for a relapse in your symptoms.

    Do not stop taking clozapine or change your dose without talking with your healthcare provider first.

    For clozapine to work properly, it should be taken everyday as ordered by your healthcare provider.

    Are There Specific Concerns About Clozapine And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with schizophrenia who wish to become pregnant face important decisions. This is a complex decision since untreated schizophrenia has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Antipsychotic use during the third trimester of pregnancy has a risk for abnormal muscle movements (extrapyramidal symptoms [EPS]) and/or withdrawal symptoms in newborns following delivery. Symptoms in the newborn may include agitation, feeding disorder, hypertonia, hypotonia, respiratory distress, somnolence, and tremor; these effects may be self-limiting or require hospitalization.

    Caution is advised with breastfeeding since clozapine does pass into breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Clozapine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you ever had muscle stiffness, shaking, tardive dyskinesia, neuroleptic malignant syndrome, or weight gain caused by a medication
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any psychiatric or medical problems you have, such as heart rhythm problems, long QT syndrome, heart attacks, diabetes, high cholesterol, or seizures
    If you have a family history of diabetes or heart disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you smoke, drink alcohol, or use illegal drugs


    How Should I Take Clozapine?
    Clozapine is usually taken 1 or 2 times per day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks. Only your healthcare provider can determine the correct dose for you.

    Clozapine orally disintegrating tablets must remain in their original packaging. Open the package with clean dry hands before each dose. Do not put tablets in a pillbox if you take the orally disintegrating tablets.

    Clozapine orally disintegrating tablets will dissolve in your mouth within seconds and can be swallowed with or without liquid.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Clozapine?
    If you miss a dose of clozapine, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed. If you miss more than 2 days of medication, contact your prescriber because he/she may need to adjust your dose.

    What Should I Avoid While Taking Clozapine?
    Avoid drinking alcohol or using illegal drugs while you are taking clozapine. They may decrease the benefits (e.g. worsen your confusion) and increase adverse effects (e.g. sedation) of the medication.

    What Happens If I Overdose With Clozapine?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of clozapine does not exist.

    What Are Possible Side Effects Of Clozapine?
    Common side effects

    Increased heart rate, low blood pressure, high blood pressure, drowsiness, sedation, dizziness, insomnia, vertigo, increased salivation, weight gain, constipation, nausea, vomiting, indigestion, fever

    Rare/serious side effects

    Decreased white blood cells, inflammation of heart muscle, seizures, severely low blood pressure, urinary incontinence

    Clozapine may increase the blood levels of a hormone called prolactin. Side effects of increased prolactin levels include females losing their period, production of breast milk and males losing their sex drive or possibly experiencing erectile problems. Long term (months or years) elevated prolactin levels can lead to osteoporosis, or increased risk of bone fractures.

    Some people may develop muscle related side effects while taking clozapine. The technical terms for these are “extrapyramidal symptoms” (EPS) and “tardive dyskinesia” (TD). Symptoms of EPS include restlessness, tremor, and stiffness. TD symptoms include slow or jerky movements that one cannot control, often starting in the mouth with tongue rolling or chewing movements.

    Temperature regulation: Impaired core body temperature regulation may occur; caution with strenuous exercise, heat exposure, and dehydration.

    Second generation antipsychotics (SGAs) increase the risk of weight gain, high blood sugar, and high cholesterol. This is also known as metabolic syndrome. Your healthcare provider may ask you for a blood sample to check your cholesterol, blood sugar, and hemoglobin A1c (a measure of blood sugar over time) while you take this medication.

    Information on healthy eating and adding exercise to decrease your chances of developing metabolic syndrome may be found at the following sites:

    http://www.helpguide.org/articles/healthy-eating/healthy-eating.htm
    http://www.helpguide.org/home-pages/exercise-fitness.htm
    SGAs have been linked with higher risk of death, strokes, and transient ischemic attacks (TIAs) in elderly people with behavior problems due to dementia.

    All antipsychotics have been associated with the risk of sudden cardiac death due to an arrhythmia (irregular heartbeat). To minimize this risk, antipsychotic medications should be used in the smallest effective dose when the benefits outweigh the risks. Your doctor may order an EKG to monitor for irregular heartbeat.

    Neuroleptic malignant syndrome is a rare, life threatening adverse effect of antipsychotics which occurs in

    All antipsychotics can cause sedation, dizziness, or orthostatic hypotension (a drop in blood pressure when standing up from sitting or lying down). These side effects may lead to falls which could cause bone fractures or other injuries. This risk is higher for people with conditions or other medications that could worsen these effects. If falls or any of these symptoms occur, contact your healthcare provider.

    Severe and life-threatening hepatoxicity (liver damage) has been reported in patients taking clozapine. Symptoms of hepatoxicity could include fatigue, weakness, loss of appetite, nausea, jaundice (yellowing of the skin), and confusion. If these symptoms occur, contact your healthcare provider immediately.

    Are There Any Risks For Taking Clozapine For Long Periods Of Time?
    Tardive dyskinesia (TD) is a side effect that develops with prolonged use of antipsychotics. Medications such as clozapine have been shown to have a lower risk of TD compared to older antipsychotics, such as Haldol® (haloperidol). If you develop symptoms of TD, such as grimacing, sucking, and smacking of lips, or other movements that you cannot control, contact your healthcare provider immediately. All patients taking either first or second generation antipsychotics should have an Abnormal Involuntary Movement Scale (AIMS) completed regularly by their healthcare provider to monitor for TD.

    Second generation antipsychotics (SGAs) increase the risk of diabetes, weight gain, high cholesterol, and high triglycerides. (See “Serious Side Effects” section for monitoring recommendations.)

    What Other Medications May Interact With Clozapine?
    Clozapine may lower your blood pressure. Medications used to lower blood pressure may increase this effect and increase your risk of falling. Propranolol (Inderal®) is an example of this type of medication.

    The following medications may increase the risk of heart problems when used with clozapine:

    Antipsychotics, such as chlorpromazine (Thorazine®), thioridizine (Mellaril®), iloperidone (Fanapt®), asenapine (Saphris®) paliperidone (Invega®), quetiapine (Seroquel®), ziprasidone (Geodon®)
    Antiarrhythmics (heart rhythm medications), such as procainamide, quinidine, amiodarone (Cordarone®), dronedarone (Multaq®), sotalol (Betapace®)
    The following medications may increase the levels and effects of clozapine: ciprofloxacin (Cipro®), fluvoxamine (Luvox®) and lamotrigine (Lamictal®)

    The following medications may decrease the levels and effects of clozapine: carbamazepine (Tegretol®), phenytoin (Dilantin®), phenobarbital, and rifampin (Rifadin®)

    Cigarette smoke can decrease levels of clozapine by as much as 50%. Let your healthcare provider know if you start or stop smoking cigarettes. Nicotine patches do not impact clozapine levels.

    How Long Does It Take For Clozapine To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking clozapine. It will probably take several weeks to see big enough changes in your symptoms to decide if clozapine is the right medication for you.

    Antipsychotic treatment is generally needed lifelong for persons with schizophrenia. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Hallucinations, disorganized thinking, and delusions may improve in the first 1-2 weeks
    Sometimes these symptoms do not completely go away
    Motivation and desire to be around other people can take at least 1-2 weeks to improve
    Symptoms continue to get better the longer you take clozapine
    It may take 2-3 months before you get the full benefit of clozapine


    Summary Of FDA Black Box Warnings
    Agranulocytosis

    Less than 1% of patients taking clozapine may develop a condition called agranulocytosis. Agranulocytosis causes the body to make fewer white blood cells. A decrease in white blood cells increases the risk of infection. If this occurs, it is reversible by stopping clozapine.

    The clozapine Risk Evaluation and Mitigation Strategy (REMS) program has been recently updated.  Your doctor will inform you whether these changes will affect your scheduled blood work.  Blood counts are checked every week for the first 6 months and every two weeks for the next 6 months.  After the first year of treatment, blood counts are checked monthly.  The pharmacy must have a copy of your blood counts to be able to dispense the medication.

    Myocarditis, Cardiomyopathy, and Mitral Valve Incompetence

    Myocarditis (inflammation of heart muscle) and cardiomyopathy (enlarged heart) have rarely been reported. This condition could be fatal. Symptoms of these heart problems include shortness of breath, racing heart, flu-like symptoms, or chest pain. Contact your healthcare provider right away if these symptoms occur.

    Seizures

    Dose-dependent seizures have been associated with clozapine (i.e. more likely with high doses or rapid dose increases). Clozapine should be used with caution in patients with a history of seizures, head injury or alcohol dependence.

    Orthostatic hypotension

    Clozapine may cause a significant drop in blood pressure when changing position from sitting to standing. Notify your prescriber if you feel lightheaded when standing up.

    Increased mortality in elderly patients with dementia-related psychosis

    Both first generation (typical) and second generation (atypical) antipsychotics are associated with an increased risk of mortality in elderly patients when used for dementia related psychosis.
    Although there were multiple causes of death in studies, most deaths appeared to be due to cardiovascular causes (e.g. sudden cardiac death) or infection (e.g. pneumonia).
    Antipsychotics are not indicated for the treatment of dementia-related psychosis.

  • Prolixin (Fluphenazine)

    Brand name: Prolixin®

    Tablet: 1 mg, 2.5 mg, 5 mg, 10 mg
    Liquid: Oral 0.5 mg/mL; Concentrate: 5 mg/mL
    Injection: Fluphenazine hydrochloride (short-acting) 2.5 mg/mL; fluphenazine decanoate (long-acting) 25 mg/mL
    Generic name: fluphenazine (floo fen uh zeen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Fluphenazine And What Does It Treat?
    Fluphenazine is a medication that treats schizophrenia. It is also known as a first generation antipsychotic (FGA) or typical antipsychotic. Fluphenazine rebalances dopamine to improve thinking, mood, and behavior.

    Symptoms of schizophrenia include:

    Hallucinations — imagined voices or images that seem real
    Delusions — beliefs that are not true (e.g., other people are reading your thoughts)
    Disorganized thinking or trouble organizing your thoughts and making sense
    Little desire to be around other people
    Trouble speaking clearly
    Lack of motivation
    Fluphenazine may help some or all of these symptoms.

    Fluphenazine may also be helpful when prescribed "off-label" for other mental health conditions. "Off-label" means that it has not been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an "off-label" treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Fluphenazine?
    Schizophrenia requires long-term treatment. Do not stop taking fluphenazine, even when you feel better.

    With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of fluphenazine may increase your risk for a relapse in your symptoms.

    Do not stop taking fluphenazine or change your dose without talking to with your healthcare provider first.

    For fluphenazine to work properly, the tablet form should be taken every day as ordered by your healthcare provider. The long-acting injectable form should be received every 2-3 weeks as ordered by your healthcare provider. It is the same medication as in the tablet form.

    Are There Specific Concerns About Fluphenazine And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with schizophrenia who wish to become pregnant face important decisions. This is a complex decision since untreated schizophrenia has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Antipsychotic use during the third trimester of pregnancy has a risk for abnormal muscle movements (extrapyramidal symptoms [EPS]) and/or withdrawal symptoms in newborns following delivery. Symptoms in the newborn may include agitation, feeding disorder, hypertonia, hypotonia, respiratory distress, somnolence, and tremor; these effects may be self-limiting or require hospitalization.

    Breast-feeding is not recommended since fluphenazine does pass into breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Fluphenazine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you ever had muscle stiffness, shaking, tardive dyskinesia, neuroleptic malignant syndrome, or weight gain caused by a medication
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any psychiatric or medical problems you have, such as heart rhythm problems, long QT syndrome, heart attacks, diabetes, high cholesterol, or seizures
    If you have a family history of diabetes or heart disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you smoke, drink alcohol, or use illegal drugs


    How Should I Take Fluphenazine?
    Fluphenazine is usually taken once or twice daily with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 2.5 mg to 10 mg. The dose of the long-acting injection ranges from 12.5 mg to 37.5 mg every 2-3 weeks. Only your healthcare provider can determine the correct dose for you.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    The long-acting injection form of fluphenazine is administered every 2-3 weeks. Your healthcare provider will administer these injections. The medication effects last for approximately 2-3 weeks.

    Fluphenazine liquid suspension should be measured with a dosing spoon or oral syringe, which you can get from your pharmacy.

    What Happens If I Miss A Dose Of Fluphenazine?
    If you miss a dose of fluphenazine, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed. If you miss a dose of fluphenazine long-acting injection, see your healthcare provider to receive your dose as soon as possible.

    What Should I Avoid While Taking Fluphenazine?
    Avoid drinking alcohol or using illegal drugs while you are taking fluphenazine. They may decrease the benefits (e.g. worsen your confusion) and increase adverse effects (e.g. sedation) of the medication.

    What Happens If I Overdose With Fluphenazine?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of fluphenazine does not exist.

    What Are Possible Side Effects Of Fluphenazine?
    Common side effects

    Rapid heartbeat, constipation, blurry vision, dry mouth, drop in blood pressure upon standing, feeling drowsy, dizzy, or restless

    Patients receiving fluphenazine decanoate long-acting injection may notice some pain at the site of the injection. This pain should resolve after a few days.

    Rare/serious side effects

    Fluphenazine may increase the blood levels of a hormone called prolactin. Side effects of increased prolactin levels include females losing their period, production of breast milk and males losing their sex drive or possibly experiencing erectile problems. Long term (months or years) elevated prolactin can lead to osteoporosis or increased risk of bone fractures.

    Some people may develop muscle related side effects while taking fluphenazine. The technical terms for these are "extrapyramidal symptoms" (EPS) and "tardive dyskinesia" (TD). Symptoms of EPS include restlessness, tremor, and stiffness. TD symptoms include slow or jerky movements that one cannot control, often starting in the mouth with tongue rolling or chewing movements.

    Temperature regulation: Impaired core body temperature regulation may occur; caution with strenuous exercise, heat exposure, and dehydration.

    All antipsychotics have been associated with the risk of sudden cardiac death due to an arrhythmia (irregular heartbeat). To minimize this risk, antipsychotic medications should be used in the smallest effective dose when the benefits outweigh the risks. Your doctor may order an EKG to monitor for irregular heartbeat.

    Neuroleptic malignant syndrome is a rare, life threatening adverse effect of antipsychotics which occurs in

    All antipsychotics can cause sedation, dizziness, or orthostatic hypotension (a drop in blood pressure when standing up from sitting or lying down). These side effects may lead to falls which could cause bone fractures or other injuries. This risk is higher for people with conditions or other medications that could worsen these effects. If falls or any of these symptoms occur, contact your healthcare provider.

    Are There Any Risks For Taking Fluphenazine For Long Periods Of Time?
    Tardive dyskinesia (TD) is a side effect that develops with prolonged use of antipsychotics. If you develop symptoms of TD, such as grimacing, sucking, and smacking of lips, or other movements that you cannot control, contact your healthcare provider immediately. All patients taking either first or second generation antipsychotics should have an Abnormal Involuntary Movement Scale (AIMS) completed regularly by their healthcare provider to monitor for TD.

    What Other Medications May Interact With Fluphenazine?
    Fluphenazine may block the effects of agents used to treat Parkinson’s disease such as levodopa/carbidopa (Sinemet®), bromocriptine, pramipexole (Mirapex®), ropinirole (Requip®), and others.

    Fluphenazine may lower your blood pressure. Medications used to lower blood pressure may increase this effect and increase your risk of falling. Propranolol (Inderal®) is an example of this type of medication.

    The following medications may increase the risk of heart problems when used with fluphenazine:

    Antipsychotics including chlorpromazine (Thorazine®), thioridizine (Mellaril®), iloperidone (Fanapt®), paliperidone (Invega®), pimozide (Orap®), quetiapine (Seroquel®), and ziprasidone (Geodon®).
    Antiarrhythmics (heart rhythm medications) including procainamide, quinidine, amiodarone (Cordarone®), dronedarone (Multaq®), and sotalol (Betapace®).
    Metoclopramide (Reglan®) may increase the risk of EPS or TD when used in combination with fluphenazine.

    The following medications may increase the levels and effects of fluphenazine: bupropion (Wellbutrin®) fluoxetine (Prozac®), duloxetine (Cymbalta®), and paroxetine (Paxil®).

    How Long Does It Take For Fluphenazine To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking fluphenazine. It will probably take several weeks to see big enough changes in your symptoms to decide if fluphenazine is the right medication for you. If you take the fluphenazine long-acting injection, it will take a few days before fluphenazine is fully absorbed and at an adequate level to begin treating your symptoms. After starting fluphenazine long-acting injection for the first time, or re-starting after a time of no medication, your provider may also have you take fluphenazine tablets for a few days.

    Antipsychotic treatment is generally needed lifelong for persons with schizophrenia. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Hallucinations, disorganized thinking, and delusions may improve in the first 1-2 weeks
    Sometimes these symptoms do not completely go away
    Motivation and desire to be around other people can take at least 1-2 weeks to improve
    Symptoms continue to get better the longer you take fluphenazine
    It may take 2-3 months before you get the full benefit of fluphenazine


    Summary Of FDA Black Box Warnings
    Increased mortality in elderly patients with dementia-related psychosis

    Both first generation (typical) and second generation (atypical) antipsychotics are associated with an increased risk of mortality in elderly patients when used for dementia related psychosis.
    Although there were multiple causes of death in studies, most deaths appeared to be due to cardiovascular causes (e.g. sudden cardiac death) or infection (e.g. pneumonia).
    Antipsychotics are not indicated for the treatment of dementia-related psychosis.​

  • Zoloft (Sertraline)

    Brand name: Zoloft®

    Tablets: 25 mg, 50 mg, 100 mg
    Liquid: 20 mg/mL

    Generic name: sertraline (SER tra leen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Sertraline And What Does It Treat?
    Sertraline is an antidepressant medication that works in the brain. It is approved for the treatment of major depressive disorder (MDD), posttraumatic stress disorder (PTSD), premenstrual dysphoric disorder (PMDD), panic disorder, and social anxiety disorder. It is also approved to treat obsessive-compulsive disorder (OCD) in adults, children and adolescents aged 6-17 years.

    Symptoms of depression include:

    Depressed mood - feeling sad, empty, or tearful
    Feeling worthless, guilty, hopeless, and helpless
    Loss of interest or pleasure in your usual activities
    Sleep and eat more or less than usual (for most people it is less)
    Low energy, trouble concentrating, or thoughts of death (suicidal thinking)
    Psychomotor agitation (‘nervous energy’)
    Psychomotor retardation (feeling like you are moving and thinking in slow motion)
    Suicidal thoughts or behaviors

    PTSD occurs when a person experiences a traumatic event (e.g., assault, combat experience) and then later feels on edge; avoids situations that remind them of the event; and experiences flashbacks or nightmares.

    PMDD is a condition where a woman experiences depression, tension, and irritability for a few days prior to menstruation that end when menstruation begins. These symptoms are more severe than those of premenstrual syndrome (PMS).

    Panic Disorder occurs when a person experiences unexpected and repeated episodes of intense fear. These episodes have physical symptoms including chest pain, shortness of breath, heart palpitations, sweating, dizziness, and nausea. Fear of future episodes is also part of panic disorder.

    Obsessive Compulsive Disorder (OCD) occurs when a person experiences the following symptoms at the same time:

    Obsessions (unwanted, recurrent, and disturbing thoughts)
    Compulsions (repetitive, ritualized behaviors that the person feels driven to perform in order to lessen the anxiety produced by the obsessions)

    Social phobia/social anxiety disorder is a fear of situations where one may feel as if they are being judged by others. Symptoms include:

    Blushing
    Difficulty talking
    Nausea
    Sweating
    Shaking

    Sertraline may also be helpful when prescribed “off-label” for binge-eating disorder, bulimia nervosa, and generalized anxiety disorder (GAD). “Off-label” means that it hasn't been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending any “off-label” treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Sertraline?
    Do not stop taking sertraline, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of sertraline may increase your risk for relapse in your symptoms.

    Stopping sertraline abruptly may result in one or more of the following withdrawal symptoms: irritability, nausea, feeling dizzy, vomiting, nightmares, headache, and/or paresthesias (prickling, tingling sensation on the skin).

    Depression is also a part of bipolar illness. People with bipolar disorder who take antidepressants may be at risk for "switching" from depression into mania. Symptoms of mania include "high" or irritable mood, very high self-esteem, decreased need for sleep, pressure to keep talking, racing thoughts, being easily distracted, frequently involved in activities with a large risk for bad consequences (for example, excessive buying sprees).

    Medical attention should be sought if serotonin syndrome is suspected. Please refer to serious side effects for signs/symptoms.

    Are There Specific Concerns About Sertraline And Pregnancy?
    If you are planning on becoming pregnant, notify your health care provider to best manage your medications. People living with MDD who wish to become pregnant face important decisions. Untreated MDD has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers. For women who take antidepressant medications during weeks 13 through the end of their pregnancy (second and third trimesters), there is a risk that the baby can be born before it is fully developed (before 37 weeks).

    For mothers who have taken SSRIs during their pregnancy, there appears to be less than a 1% chance of infants developing persistent pulmonary hypertension. This is a potentially fatal condition that is associated with use of the antidepressant in the second half of pregnancy. However, women who discontinued antidepressant therapy were five times more likely to have a depression relapse than those who continued their antidepressant. If you are pregnant, please discuss the risks and benefits of antidepressant use with your health care provider.

    Caution is advised with breastfeeding since sertraline does pass into breast milk.

    What Should I Discuss With My Health Care Provider Before Taking Sertraline?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any other psychiatric or medical problems you have, including a history of bipolar disorder
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breastfeeding
    If you drink alcohol or use drugs

    How Should I Take Sertraline?
    Sertraline is usually taken one time per day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The dose usually ranges from 50 mg to 200 mg. Only your health care provider can determine the correct dose for you.

    If you are taking it for PMDD, sertraline can be taken once daily (everyday) or intermittently (usually starting 14 days prior to menstruation through the first full day of menses of each cycle).

    The liquid should be measured with an oral syringe or dropper which you can get from your pharmacy. It should be added to 4 ounces of water, ginger ale, lemon/lime soda, lemonade, or orange juice immediately prior to taking the medication. It should not be mixed in advance.

    Consider using a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Sertraline?
    If you miss a dose of sertraline, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your health care provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Sertraline?
    Avoid drinking alcohol or using illegal drugs while you are taking antidepressant medications. They may decrease the benefits (e.g., worsen your condition) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Sertraline?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of sertraline does not exist.

    What Are The Possible Side Effects Of Sertraline?
    Common side effects

    Headache, nausea, diarrhea, dry mouth, increased sweating
    Feeling nervous, restless, fatigued, sleepy or having trouble sleeping (insomnia)
    These will often improve over the first week or two as you continue to take the medication.

    Sexual side effects, such as problems with orgasm or ejaculatory delay often do not diminish over time.

    Rare/serious side effects

    Low sodium blood levels (symptoms of low sodium levels may include headache, weakness, difficulty concentrating and remembering), teeth grinding, angle closure glaucoma (symptoms of angle closure glaucoma may include eye pain, changes in vision, swelling or redness in or around eye).

    Serotonin syndrome (symptoms may include shivering, diarrhea, confusion, severe muscle tightness, fever, seizures, and death), seizure

    SSRI antidepressants including sertraline may increase the risk of bleeding events. Combined use of aspirin, nonsteroidal anti-inflammatory drugs (e.g., ibuprofen, naproxen), warfarin, and other anti-coagulants may increase this risk. This may include gums that bleed more easily, nose bleed, or gastrointestinal bleeding. Some cases have been life threatening.

    Are There Any Risks For Taking Sertraline For Long Periods Of Time?
    To date, there are no known problems associated with long term use of sertraline. It is a safe and effective medication when used as directed.

    What Other Medications May Interact With Sertraline?
    Sertraline should not be taken with or within two weeks of taking monoamine oxidase inhibitors (MAOIs). These include phenelzine (Nardil®), tranylcypromine (Parnate®), isocarboxazid (Marplan®), rasagiline (Azilect®), and selegiline (Emsam®).

    Although rare, there is an increased risk of serotonin syndrome when sertraline is used with other medications that increase serotonin, such as other antidepressants, migraine medications called “triptans” (e.g., Imitrex®), some pain medications (e.g., tramadol (Ultram®)), and the antibiotic linezolid (Zyvox®).

    Sertraline should not be taken with pimozide (Orap®).

    Sertraline may increase the effects of other medications that can cause bleeding (e.g., ibuprofen (Advil®, Motrin®), warfarin (Coumadin®) and aspirin).

    Sertraline liquid should NOT be taken in combination with disulfiram (Antabuse®) due to the alcohol content of the concentrate.

    How Long Does It Take For Sertraline To Work?
    Sleep, energy, or appetite may show some improvement within the first 1-2 weeks. Improvement in these physical symptoms can be an important early signal that the medication is working. Depressed mood and lack of interest in activities may need up to 6-8 weeks to fully improve.

    Summary Of FDA Black Box Warnings
    Suicidal thoughts or actions in children and adults

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide. Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking antidepressant medications. This risk may persist until significant remission occurs.

    In short-term studies, antidepressants increased the risk of suicidality in children, adolescents, and young adults when compared to placebo. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24. Adults age 65 and older taking antidepressants have a decreased risk of suicidality. Patients, their families, and caregivers should be alert to the emergence of anxiety, restlessness, irritability, aggressiveness and insomnia. If these symptoms emerge, they should be reported to the patient’s prescriber or health care professional. All patients being treated with antidepressants for any indication should watch for and notify their health care provider for worsening symptoms, suicidality and unusual changes in behavior, especially during the first few months of treatment.

  • Abilify (Aripiprazole) 

    Abilify®Tablets: 2 mg, 5mg, 10 mg, 15 mg, 20 mg, 30 mg
    Oral disintegrating: 10 mg, 15 mg
    Solution: 1 mg/mL
    Abilify MyCite®Tablet with a digestible sensor: 2 mg, 5 mg, 10 mg, 15 mg, 20 mg, 30 mg
    Abilify Maintena®Extended-release injectable suspension: 300 mg, 400 mg
    Abilify Aristada® (aripiprazole lauroxil)Extended-release injectable suspension: 441 mg, 662 mg, 882 mg
    Aristada Initio® (aripiprazole lauroxil)Extended-release injectable suspension: 675 mg
    Generic name: aripiprazole (ay ri PIP ray zole), aripiprazole lauroxil (law rox il)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Aripiprazole And What Does It Treat?
    Aripiprazole is a medication that works in the brain to treat schizophrenia. It is also known as a second generation antipsychotic (SGA) or atypical antipsychotic. Aripiprazole rebalances dopamine and serotonin to improve thinking, mood, and behavior.

    Symptoms of schizophrenia include:

    Hallucinations — imagined voices or images that seem real
    Delusions — beliefs that are not true (e.g., other people are reading your thoughts)
    Disorganized thinking or trouble organizing your thoughts and making sense
    Little desire to be around other people
    Trouble speaking clearly
    Lack of motivation
    Aripiprazole may help some or all of these symptoms.

    Aripiprazole is also FDA approved for the following indications:

    Acute treatment of manic or mixed episodes of bipolar disorder (when used alone or with lithium or valproate)
    Maintenance (long-term) treatment of bipolar disorder
    Adjunctive treatment of major depressive disorder. This means aripiprazole is used in addition to an antidepressant to help treat depression.
    Irritability associated with autistic disorders
    Tourette syndrome
    Acute treatment of agitation in schizophrenia and bipolar disorder
    This medication sheet will focus primarily on schizophrenia. Find more information about bipolar disorder, depression and autism spectrum disorders here.

    Aripiprazole may also be helpful when prescribed “off-label” for borderline personality disorder or drug-induced hyperprolactinemia (elevated prolactin levels caused by other antipsychotics). “Off-label” means that it hasn’t been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an “off-label” treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Aripiprazole?
    Schizophrenia requires long-term treatment. Do not stop taking aripiprazole, even when you feel better. With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of aripiprazole may increase your risk for a relapse in your symptoms. Do not stop taking aripiprazole or change your dose without talking to with your healthcare provider first. For aripiprazole to work properly, it should be taken every day as ordered by your healthcare provider.

    Are There Specific Concerns About Aripiprazole And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with schizophrenia who wish to become pregnant face important decisions. This is a complex decision since untreated schizophrenia has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Antipsychotic use during the third trimester of pregnancy has a risk for abnormal muscle movements (extrapyramidal symptoms [EPS]) and/or withdrawal symptoms in newborns following delivery. Symptoms in the newborn may include agitation, feeding disorder, hypertonia, hypotonia, respiratory distress, somnolence, and tremor; these effects may be self-limiting or require hospitalization.

    In general, infants exposed to SGAs via breast milk should be monitored weekly for the first month of exposure for symptoms, such as appetite changes, insomnia, irritability, or lethargy.

    Caution is advised with breastfeeding since aripiprazole does pass into breast milk.

    What Should I Discuss With My Healthcare Provider Before Taking Aripiprazole?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you ever had muscle stiffness, shaking, tardive dyskinesia, neuroleptic malignant syndrome, or weight gain caused by a medication
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication
    Any psychiatric or medical problems you have, such as heart rhythm problems, long QT syndrome, heart attacks, diabetes, high cholesterol, or seizures
    If you have a family history of diabetes or heart disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you smoke, drink alcohol, or use illegal drugs


    How Should I Take Aripiprazole?
    Aripiprazole tablets and suspension are usually taken 1 time per day with or without food. Typically, patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The oral dose aripiprazole usually ranges from 2 mg to 30 mg taken once daily. The dose of aripiprazole maintena extended-release injection ranges from 300 mg to 400 mg given once monthly; the dose of aripiprazole lauroxil extended-release injection ranges from 441 mg to 1064 mg — depending on the dose, it is given once per month, every 6 weeks, or every 2 months. Aripiprazole maintena requires a two-week oral medication overlap; aripiprazole lauroxil requires a three-week oral overlap. Aripiprazole lauroxil Initio is typically given after an oral dose of aripiprazole along with an aripiprazole lauroxil injection – this allows for a one-day initiation and does not require further oral overlap. Only your healthcare provider can determine the correct formulation and dose for you.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Aripiprazole?
    If you miss a dose of aripiprazole, take it as soon as you remember, unless it is closer to the time of your next dose. Do not double your next dose or take more than what is prescribed. If you miss an injection, call your doctor or pharmacist right away. Discuss this with your healthcare provider.

    What Should I Avoid While Taking Aripiprazole?
    Avoid drinking alcohol or using illegal drugs while you are taking aripiprazole. They may decrease the benefits (e.g., worsen your confusion) and increase adverse effects (e.g., sedation) of the medication.

    What Happens If I Overdose With Aripiprazole?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222. A specific treatment to reverse the effects of aripiprazole does not exist.

    What Are Possible Side Effects Of Aripiprazole?
    Common side effects

    Headache, extrapyramidal symptoms, drowsiness, restlessness, fatigue, sedation, agitation, insomnia, anxiety, weight gain, cholesterol abnormalities, increased glucose, nausea, vomiting, constipation, application site rash (MyCite), tremor

    Rare/serious side effects

    Rash, dry mouth, muscle aches, seizure, agitation

    Aripiprazole may increase the blood levels of a hormone called prolactin. Side effects of increased prolactin levels include females losing their period, production of breast milk and males losing their sex drive or possibly experiencing erectile problems. Long term (months or years) of elevated prolactin can lead to osteoporosis or increased risk of bone fractures.

    Some people may develop muscle-related side effects while taking aripiprazole. The technical terms for these are “extrapyramidal symptoms” (EPS) and “tardive dyskinesia” (TD). Symptoms of EPS include restlessness, tremor, and stiffness. TD symptoms include slow or jerky movements that one cannot control, often starting in the mouth with tongue rolling or chewing movements.

    Temperature regulation: Impaired core body temperature regulation may occur; caution with strenuous exercise, heat exposure, and dehydration.

    Second generation antipsychotics (SGAs) increase the risk of weight gain, high blood sugar, and high cholesterol. This is also known as metabolic syndrome. Your healthcare provider may ask you for a blood sample to check your cholesterol, blood sugar, and hemoglobin A1c (a measure of blood sugar over time) while you take this medication.

    Information on healthy eating and adding exercise to decrease your chances of developing metabolic syndrome may be found at the following sites:

    http://www.helpguide.org/articles/healthy-eating/healthy-eating.htm
    http://www.helpguide.org/home-pages/exercise-fitness.htm
    SGAs have been linked with higher risk of death, strokes, and transient ischemic attacks (TIAs) in elderly people with behavior problems due to dementia.

    All antipsychotics have been associated with the risk of sudden cardiac death due to an arrhythmia (irregular heart beat). To minimize this risk, antipsychotic medications should be used in the smallest effective dose when the benefits outweigh the risks. Your doctor may order an EKG to monitor for irregular heartbeat.

    Neuroleptic malignant syndrome is a rare, life threatening adverse effect of antipsychotics which occurs in

    All antipsychotics can cause sedation, dizziness, or orthostatic hypotension (a drop in blood pressure when standing up from sitting or lying down). These side effects may lead to falls which could cause bone fractures or other injuries. This risk is higher for people with conditions or other medications that could worsen these effects. If falls or any of these symptoms occur, contact your healthcare provider.

    The U.S. Food and Drug Administration (FDA) is warning that compulsive or uncontrollable urges to gamble, binge eat, shop, and have sex have been reported with the use of aripiprazole. These uncontrollable urges were reported to have stopped when the medicine was discontinued or the dose was reduced. These impulse-control problems are rare, but they may result in harm to the patient and others if not recognized.

    Are There Any Risks For Taking Aripiprazole For Long Periods Of Time?
    Tardive dyskinesia (TD) is a side effect that develops with prolonged use of antipsychotics. Medications such as aripiprazole have been shown to have a lower risk of TD compared to older antipsychotics, such as Haldol (haloperidol). If you develop symptoms of TD, such as grimacing, sucking, and smacking of lips, or other movements that you cannot control, contact your healthcare provider immediately. All patients taking either first or second generation antipsychotics should have an Abnormal Involuntary Movement Scale (AIMS) completed regularly by their healthcare provider to monitor for TD.

    Second generation antipsychotics (SGAs) increase the risk of diabetes, weight gain, high cholesterol, and high triglycerides. (See “Serious Side Effects” section for monitoring recommendations.

    What Other Medications May Interact With Aripiprazole?
    The following medications may increase the levels and effects of aripiprazole:

    The antibiotic clarithromycin (Biaxin®)
    Antidepressants, such as fluoxetine (Prozac®), paroxetine (Paxil®), and nefazodone
    Antifungals, such as fluconazole (Diflucan®), ketoconazole (Nizoral®), and itraconazole (Sporanox®)
    The antiarrhymia agent quinidine
    HIV medications, such as the protease inhibitors indinavir (Crixivan®), ritonavir (Norvir®), saquinavir (Fortovase®, Invirase®), and lopinavir/ritonavir (Kaletra®)
    The following medications may decrease the levels and effects of aripiprazole:

    carbamazepine (Tegretol®)
    rifampin (Rifadin®)


    How Long Does It Take For Aripiprazole To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking aripiprazole. It will probably take several weeks to see big enough changes in your symptoms to decide if aripiprazole is the right medication for you.

    Antipsychotic treatment is generally needed lifelong for persons with schizophrenia. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Hallucinations, disorganized thinking, and delusions may improve in the first 1-2 weeks
    Sometimes these symptoms do not completely go away
    Motivation and desire to be around other people can take at least 1-2 weeks to improve
    Symptoms continue to get better the longer you take aripiprazole
    It may take 2-3 months before you get the full benefit of aripiprazole


    Summary Of FDA Black Box Warnings
    Increased mortality in elderly patients with dementia-related psychosis

    Both first generation (typical) and second generation (atypical) antipsychotics are associated with an increased risk of mortality in elderly patients when used for dementia related psychosis. Although there were multiple causes of death in studies, most deaths appeared to be due to cardiovascular causes (e.g. sudden cardiac death) or infection (e.g. pneumonia). Antipsychotics are not indicated for the treatment of dementia-related psychosis.

    Suicidal Thoughts or Actions in Children, Teens, and Young Adults

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide. Patients treated with antidepressants may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking medications. This risk may persist until significant remission occurs. Patients, their families, and caregivers should be alert to the emergence of anxiety, restlessness, irritability, aggressiveness and insomnia. If these symptoms emerge, they should be reported to the patient’s prescriber or healthcare professional. All patients being treated with this medication for depression should watch for and notify their healthcare provider for worsening symptoms, suicidality and unusual changes in behavior, especially during the first few months of treatment.

  • Zyprexa (Olanzapine)

    Brand names:

    Zyprexa®Tablet: 2.5 mg, 5 mg, 7.5 mg, 10 mg, 15 mg, 20 mg
    Injection (immediate release): 10 mg vials
    Zyprexa Zydix®Orally disintegrating tablet: 5 mg, 10 mg, 15 mg, 20 mg
    Zyprexa Relprevv®Injection (extended release): 150 mg, 210 mg, 300 mg, 405 mg
    Generic name: olanzapine (oh LANZ a peen)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Olanzapine And What Does It Treat?
    Olanzapine is a medication that works in the brain to treat schizophrenia. It is also known as a second generation antipsychotic (SGA) or atypical antipsychotic. Olanzapine rebalances dopamine and serotonin to improve thinking, mood, and behavior.

    Symptoms of schizophrenia include:

    Hallucinations — imagined voices or images that seem real
    Delusions — beliefs that are not true (e.g., other people are reading your thoughts)
    Disorganized thinking or trouble organizing your thoughts and making sense
    Little desire to be around other people
    Trouble speaking clearly
    Lack of motivation
    Olanzapine may help some or all of these symptoms.

    Olanzapine is also FDA approved for the following indications:

    Acute treatment of manic or mixed episodes of bipolar disorder
    Maintenance (long-term) treatment of bipolar disorder
    Acute treatment of agitation in schizophrenia and bipolar disorder
    This medication sheet will focus primarily on schizophrenia. You can find more information about bipolar disorder and depression here.

    Olanzapine may also be helpful when prescribed "off-label" for prevention of chemotherapy-associated acute and delayed nausea or vomiting, chemotherapy-associated breakthrough nausea or vomiting, delirium, delusional parasitosis, post-traumatic stress disorder, Tourette syndrome, and other mental health conditions. "Off-label" means that it has not been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending and "off-label" treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Olanzapine?
    Schizophrenia requires long-term treatment. Do not stop taking olanzapine, even when you feel better.

    With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of olanzapine may increase your risk for a relapse in your symptoms.

    Do not stop taking olanzapine or change your dose without talking with your healthcare provider first.

    For olanzapine to work properly, it should be taken every day as ordered by your healthcare provider.

    Are There Specific Concerns About Olanzapine And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with schizophrenia who wish to become pregnant face important decisions. This is a complex decision since untreated schizophrenia has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Antipsychotic use during the third trimester of pregnancy has a risk for abnormal muscle movements (extrapyramidal symptoms [EPS]) and/or withdrawal symptoms in newborns following delivery. Symptoms in the newborn may include agitation, feeding disorder, hypertonia, hypotonia, respiratory distress, somnolence, and tremor; these effects may be self-limiting or require hospitalization.

    Caution is advised with breastfeeding since olanzapine does pass into breast milk. It is recommended that women receiving olanzapine should not breast-feed.

    What Should I Discuss With My Healthcare Provider Before Taking Olanzapine?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you ever had muscle stiffness, shaking, tardive dyskinesia, neuroleptic malignant syndrome, or weight gain caused by a medication
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any psychiatric or medical problems you have, such as heart rhythm problems, long QT syndrome, heart attacks, diabetes, high cholesterol, or seizures
    If you have a family history of diabetes or heart disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you smoke, drink alcohol, or use illegal drugs


    How Should I Take Olanzapine?
    Olanzapine tablets are usually taken 1 time per day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The oral dose usually ranges from 5 mg to 20 mg. The dose of the injection usually ranges from 150 mg to 405 mg. Only your healthcare provider can determine the correct dose for you.

    Olanzapine orally disintegrating tablets must remain in their original packaging. Open the package with clean dry hands before each dose. Do not try to put tablets in a pillbox if you take the orally disintegrating tablets.

    Olanzapine orally disintegrating tablets will dissolve in your mouth within seconds and can be swallowed with or without liquid.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    The long-acting injection form of olanzapine is administered every 2 to 4 weeks. It should be administered by your health care professional through an injection into your buttocks area. A health care professional will keep you in a setting where you can be observed for at least 3 hours after each injection

    What Happens If I Miss A Dose Of Olanzapine?
    If you miss a dose of olanzapine, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed. If you miss a dose of olanzapine long-acting injection, see your healthcare provider to receive your dose as soon as possible.

    What Should I Avoid While Taking Olanzapine?
    Avoid drinking alcohol or using illegal drugs while you are taking olanzapine. They may decrease the benefits (e.g. worsen your confusion) and increase adverse effects (e.g. sedation) of the medication.

    What Happens If I Overdose With Olanzapine?
    If an overdose occurs, call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of olanzapine does not exist.

    What Are Possible Side Effects Of Olanzapine?
    Common side effects

    Low blood pressure, drowsiness, extrapyramidal symptoms, restlessness, dizziness, headache, fatigue, insomnia, increased prolactin, weight gain, increased appetite, dry mouth, indigestion, constipation, liver function test abnormalities, weakness, accidental injury

    Rare/serious side effects

    Olanzapine may increase the blood levels of a hormone called prolactin. Side effects of increased prolactin levels include females losing their period, production of breast milk and males losing their sex drive or possibly experiencing erectile problems. Long term (months or years) of elevated prolactin can lead to osteoporosis, or increased risk of bone fractures.

    Some people may develop muscle related side effects while taking olanzapine. The technical terms for these are “extrapyramidal symptoms” (EPS) and “tardive dyskinesia” (TD). Symptoms of EPS include restlessness, tremor, and stiffness. TD symptoms include slow or jerky movements that one cannot control, often starting in the mouth with tongue rolling or chewing movements.

    Temperature regulation: Impaired core body temperature regulation may occur; caution with strenuous exercise, heat exposure, and dehydration.

    Second generation antipsychotics (SGAs) increase the risk of weight gain, high blood sugar, and high cholesterol. This is also known as metabolic syndrome. Your healthcare provider may ask you for a blood sample to check your cholesterol, blood sugar, and hemoglobin A1c (a measure of blood sugar over time) while you take this medication.

    Information on healthy eating and adding exercise to decrease your chances of developing metabolic syndrome may be found at the following sites:

     

    http://www.helpguide.org/articles/healthy-eating/healthy-eating.htm
    http://www.helpguide.org/home-pages/exercise-fitness.htm
    SGAs have been linked with higher risk of death, strokes, and transient ischemic attacks (TIAs) in elderly people with behavior problems due to dementia.

    All antipsychotics have been associated with the risk of sudden cardiac death due to an arrhythmia (irregular heartbeat). To minimize this risk, antipsychotic medications should be used in the smallest effective dose when the benefits outweigh the risks. Your doctor may order an EKG to monitor for irregular heartbeat.

    Neuroleptic malignant syndrome is a rare, life threatening adverse effect of antipsychotics which occurs in

    All antipsychotics can cause sedation, dizziness, or orthostatic hypotension (a drop in blood pressure when standing up from sitting or lying down). These side effects may lead to falls which could cause bone fractures or other injuries. This risk is higher for people with conditions or other medications that could worsen these effects. If falls or any of these symptoms occur, contact your healthcare provider.

    Multiorgan hypersensitivity reactions (drug reaction with eosinophilia and systemic symptoms [DRESS]): Potentially serious, sometimes fatal, multiorgan hypersensitivity reactions have been reported. Symptoms may include a rash, increased levels of certain white blood cells (eosinophils), fever, and/or swollen/enlarged lymph nodes with systemic complications. If DRESS is suspected, contact your healthcare provider immediately.

    Are There Any Risks For Taking Olanzapine For Long Periods Of Time?
    Tardive dyskinesia (TD) is a side effect that develops with prolonged use of antipsychotics. Medications such as olanzapine have been shown to have a lower risk of TD compared to older antipsychotics, such as Haldol® (haloperidol). If you develop symptoms of TD, such as grimacing, sucking, and smacking of lips, or other movements that you cannot control, contact your healthcare provider immediately. All patients taking either first or second generation antipsychotics should have an Abnormal Involuntary Movement Scale (AIMS) completed regularly by their healthcare provider to monitor for TD.

    Second generation antipsychotics (SGAs) increase the risk of diabetes, weight gain, high cholesterol, and high triglycerides. (See “Serious Side Effects” section for monitoring recommendations.)

    What Other Medications May Interact With Olanzapine?
    Olanzapine may block the effects of agents used to treat Parkinson’s disease such as levodopa/carbidopa (Sinemet®), bromocriptine, pramipexole (Mirapex®), ropinirole (Requip®), and others.

    Olanzapine may lower your blood pressure. Medications used to lower blood pressure may increase this effect. Propranolol (Inderal®) is an example of this type of medication.

    Sedative medications, such as lorazepam (Ativan®) and diazepam (Valium®) may increase the risk of dizziness or sleepiness when used in combination with olanzapine. This risk is increased when these medications are given as an injection.

    The following medications may increase the levels and effects of olanzapine: ciprofloxacin (Cipro®) and fluvoxamine (Luvox®)

    Carbamazepine (Tegretol®) may decrease the levels and effects of olanzapine.

    Cigarette (and other types of) smoke can decrease levels of olanzapine. Let your healthcare provider know if you start or stop smoking cigarettes. Nicotine patches do not impact olanzapine levels.

    How Long Does It Take For Olanzapine To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking olanzapine. It will probably take several weeks to see big enough changes in your symptoms to decide if olanzapine is the right medication for you.

    Antipsychotic treatment is generally needed lifelong for persons with schizophrenia. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Hallucinations, disorganized thinking, and delusions may improve in the first 1-2 weeks
    Sometimes these symptoms do not completely go away
    Motivation and desire to be around other people can take at least 1-2 weeks to improve
    Symptoms continue to get better the longer you take olanzapine
    It may take 2-3 months before you get the full benefit of olanzapine


    Summary Of FDA Black Box Warnings
    Increased mortality in elderly patients with dementia-related psychosis

    Both first generation (typical) and second generation (atypical) antipsychotics are associated with an increased risk of mortality in elderly patients when used for dementia related psychosis.
    Although there were multiple causes of death in studies, most deaths appeared to be due to cardiovascular causes (e.g. sudden cardiac death) or infection (e.g. pneumonia).
    Antipsychotics are not indicated for the treatment of dementia-related psychosis.
    Post-injection Delirium/Sedation Syndrome

    This rare reaction has been reported with Zyprexa Relprevv, the long-acting injection form of olanzapine. This has not been reported with olanzapine tablets.
    Signs and symptoms of post-injection delirium/sedation syndrome are similar to olanzapine overdose and include sedation (including coma) and delirium (a confusional state).
    Zyprexa Relprevv (olanzapine long-acting injection) must be given at a registered healthcare facility with access to emergency response services.
    After each injection, patients must be observed at the healthcare facility by a healthcare professional for at least 3 hours
    Zyprexa Relprevv (olanzapine long-acting injection) is available only through a restricted distribution program called Zyprexa Relprevv Patient Care Program

  • Rexulti (Brexpiprazole)

    Brand name: Rexulti®

    Tablets: 0.25 mg, 0.5 mg, 1 mg, 2 mg, 3 mg, 4 mg
    Generic name: brexipiprazole (breks PIP ray zole)

    All FDA black box warnings are at the end of this fact sheet. Please review before taking this medication.

    What Is Brexpiprazole And What Does It Treat?
    Brexpiprazole is a medication that works in the brain to treat schizophrenia. It is also known as a second generation antipsychotic (SGA) or atypical antipsychotic. Brexpiprazole rebalances dopamine and serotonin to improve thinking, mood, and behavior.

    Symptoms of schizophrenia include:

    Hallucinations — imagined voices or images that seem real
    Delusions — beliefs that are not true (e.g., other people are reading your thoughts)
    Disorganized thinking or trouble organizing your thoughts and making sense
    Little desire to be around other people
    Trouble speaking clearly
    Lack of motivation
    Brexpiprazole may help some or all of these symptoms.

    Brexpiprazole is also FDA approved for the following indications:

    Adjunctive treatment of major depressive disorder. This means brexpiprazole is used in addition to an antidepressant to help treat depression.
    This medication sheet will focus primarily on schizophrenia. You can find more information about depression here.

    Brexpiprazole may also be helpful when prescribed "off-label" for other mental health conditions. "Off-label" means that it has not been approved by the Food and Drug Administration for this condition. Your mental health provider should justify his or her thinking in recommending an "off-label" treatment. They should be clear about the limits of the research around that medication and if there are any other options.

    What Is The Most Important Information I Should Know About Brexpiprazole?
    Schizophrenia requires long-term treatment. Do not stop taking brexpiprazole, even when you feel better.

    With input from you, your health care provider will assess how long you will need to take the medicine.

    Missing doses of brexpiprazole may increase your risk for a relapse in your symptoms.

    Do not stop taking brexpiprazole or change your dose without talking with your healthcare provider first.

    For brexpiprazole to work properly, it should be taken every day as ordered by your healthcare provider.

    Are There Specific Concerns About Brexpiprazole And Pregnancy?
    If you are planning on becoming pregnant, notify your healthcare provider to best manage your medications. People living with schizophrenia who wish to become pregnant face important decisions. This is a complex decision since untreated schizophrenia has risks to the fetus, as well as the mother. It is important to discuss the risks and benefits of treatment with your doctor and caregivers.

    Antipsychotic use during the third trimester of pregnancy has a risk for abnormal muscle movements (extrapyramidal symptoms [EPS]) and/or withdrawal symptoms in newborns following delivery. Symptoms in the newborn may include agitation, feeding disorder, hypertonia, hypotonia, respiratory distress, somnolence, and tremor; these effects may be self-limiting or require hospitalization.

    Caution is advised with breastfeeding since brexpiprazole has been shown to pass into animal milk. No studies have been conducted to assess for brexpiprazole in breastfed infants or how this medicine may affect milk production.

    What Should I Discuss With My Healthcare Provider Before Taking Brexpiprazole?
    Symptoms of your condition that bother you the most
    If you have thoughts of suicide or harming yourself
    Medications you have taken in the past for your condition, whether they were effective or caused any adverse effects
    If you ever had muscle stiffness, shaking, tardive dyskinesia, neuroleptic malignant syndrome, or weight gain caused by a medication
    If you experience side effects from your medications, discuss them with your provider. Some side effects may pass with time, but others may require changes in the medication.
    Any psychiatric or medical problems you have, such as heart rhythm problems, long QT syndrome, heart attacks, diabetes, high cholesterol, or seizures
    If you have a family history of diabetes or heart disease
    All other medications you are currently taking (including over the counter products, herbal and nutritional supplements) and any medication allergies you have
    Other non-medication treatment you are receiving, such as talk therapy or substance abuse treatment. Your provider can explain how these different treatments work with the medication.
    If you are pregnant, plan to become pregnant, or are breast-feeding
    If you smoke, drink alcohol, or use illegal drugs


    How Should I Take Brexpiprazole?
    Brexpiprazole tablets are usually taken once a day with or without food.

    Typically patients begin at a low dose of medicine and the dose is increased slowly over several weeks.

    The oral dose usually ranges from 0.5 mg to 4 mg. Only your healthcare provider can determine the correct dose for you.

    Use a calendar, pillbox, alarm clock, or cell phone alert to help you remember to take your medication. You may also ask a family member or a friend to remind you or check in with you to be sure you are taking your medication.

    What Happens If I Miss A Dose Of Brexpiprazole?
    If you miss a dose of brexpiprazole, take it as soon as you remember, unless it is closer to the time of your next dose. Discuss this with your healthcare provider. Do not double your next dose or take more than what is prescribed.

    What Should I Avoid While Taking Brexpiprazole?
    Avoid drinking alcohol or using illegal drugs while you are taking brexpiprazole. They may decrease the benefits (e.g. worsen your confusion) and increase adverse effects (e.g. sedation) of the medication.

    What Happens If I Overdose With Brexpiprazole?
    If an overdose occurs call your doctor or 911. You may need urgent medical care. You may also contact the poison control center at 1-800-222-1222.

    A specific treatment to reverse the effects of brexpiprazole does not exist.

    What Are Possible Side Effects Of Brexpiprazole?
    Common side effects

    Restlessness, weight gain, cholesterol abnormalities

    Reflux or heartburn

    Rare/serious side effects

    Brexpiprazole may increase the blood levels of a hormone called prolactin. Side effects of increased prolactin levels include females losing their period, production of breast milk and males losing their sex drive or possibly experiencing erectile problems. Long term (months or years) of elevated prolactin can lead to osteoporosis, or increased risk of bone fractures.

    Some people may develop muscle-related side effects while taking brexpiprazole. The technical terms for these are “extrapyramidal symptoms” (EPS) and “tardive dyskinesia” (TD). Symptoms of EPS include restlessness, tremor, and stiffness. TD symptoms include slow or jerky movements that one cannot control, often starting in the mouth with tongue rolling or chewing movements.

    Temperature regulation: Impaired core body temperature regulation may occur; caution with strenuous exercise, heat exposure, and dehydration.

    Second generation antipsychotics (SGAs) increase the risk of weight gain, high blood sugar, and high cholesterol. This is also known as metabolic syndrome. Your healthcare provider may ask you for a blood sample to check your cholesterol, blood sugar, and hemoglobin A1c (a measure of blood sugar over time) while you take this medication.

    Information on healthy eating and adding exercise to decrease your chances of developing metabolic syndrome may be found at the following sites:http://www.helpguide.org/articles/healthy-eating/healthy-eating.htm
    http://www.helpguide.org/home-pages/exercise-fitness.htm
    SGAs have been linked with higher risk of death, strokes, and transient ischemic attacks (TIAs) in elderly people with behavior problems due to dementia.

    All antipsychotics have been associated with the risk of sudden cardiac death due to an arrhythmia (irregular heartbeat). To minimize this risk, antipsychotic medications should be used in the smallest effective dose when the benefits outweigh the risks. Your doctor may order an EKG to monitor for irregular heartbeat.

    Neuroleptic malignant syndrome is a rare, life threatening adverse effect of antipsychotics which occurs in

    All antipsychotics can cause sedation, dizziness, or orthostatic hypotension (a drop in blood pressure when standing up from sitting or lying down). These side effects may lead to falls which could cause bone fractures or other injuries. This risk is higher for people with conditions or other medications that could worsen these effects. If falls or any of these symptoms occur, contact your healthcare provider.

    Are There Any Risks For Taking Brexpiprazole For Long Periods Of Time?
    Tardive dyskinesia (TD) is a side effect that develops with prolonged use of antipsychotics. Medications such as brexpiprazole have been shown to have a lower risk of TD compared to older antipsychotics, such as Haldol® (haloperidol). If you develop symptoms of TD, such as grimacing, sucking, and smacking of lips, or other movements that you cannot control, contact your healthcare provider immediately. All patients taking either first or second generation antipsychotics should have an Abnormal Involuntary Movement Scale (AIMS) completed regularly by their healthcare provider to monitor for TD.

    Second generation antipsychotics (SGAs) increase the risk of diabetes, weight gain, high cholesterol, and high triglycerides. (See "Serious Side Effects" section for monitoring recommendations).

    What Other Medications May Interact With Brexpiprazole?
    The following medications may increase the levels and effects of brexpiprazole:

    The antibiotic clarithromycin (Biaxin®)
    Antidepressants, such as fluoxetine (Prozac®), paroxetine (Paxil®), and nefazodone
    Antifungals, such as fluconazole (Diflucan®), ketoconazole (Nizoral®), and itraconazole (Sporanox®)
    The antiarrhymia agent quinidine
    HIV medications, such as the protease inhibitors indinavir (Crixivan®), ritonavir (Norvir®), saquinavir (Fortovase®, Invirase®), and lopinavir/ritonavir (Kaletra®)
    The following medications may decrease the levels and effects of brexpiprazole:

    Some seizure medications and mood stabilizers, such as carbamazepine (Tegretol®)
    Medications used to treat tuberculosis, such as rifampin (Rifadin®)


    How Long Does It Take For Brexpiprazole To Work?
    It is very important to tell your doctor how you feel things are going during the first few weeks after you start taking brexpiprazole. It will probably take several weeks to see big enough changes in your symptoms to decide if brexpiprazole is the right medication for you.

    Antipsychotic treatment is generally needed lifelong for persons with schizophrenia. Your doctor can best discuss the duration of treatment you need based on your symptoms and illness.

    Hallucinations, disorganized thinking, and delusions may improve in the first 1-2 weeks
    Sometimes these symptoms do not completely go away
    Motivation and desire to be around other people can take at least 1-2 weeks to improve
    Symptoms continue to get better the longer you take brexpiprazole
    It may take 2-3 months before you get the full benefit of brexpiprazole


    Summary Of FDA Black Box Warnings
    Increased mortality in elderly patients with dementia-related psychosis

    Both first generation (typical) and second generation (atypical) antipsychotics are associated with an increased risk of mortality in elderly patients when used for dementia related psychosis.
    Although there were multiple causes of death in studies, most deaths appeared to be due to cardiovascular causes (e.g. sudden cardiac death) or infection (e.g. pneumonia).
    Antipsychotics are not indicated for the treatment of dementia-related psychosis.
    Suicidal thoughts or actions in children and adults

    Depression and certain other psychiatric disorders are themselves associated with increases in the risk of suicide.
    Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking medications. This risk may persist until significant remission occurs.
    Patients, their families, and caregivers should be alert to the emergence of anxiety, restlessness, irritability, aggressiveness and insomnia. If these symptoms emerge, they should be reported to the patient’s prescriber or healthcare professional.
    All patients being treated with this medication for depression should watch for and notify their healthcare provider for worsening symptoms, suicidality and unusual changes in behavior, especially during the first few months of treatment.

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