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Lunesta

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Brand Name: Lunesta
Other brand Name(s):
Generic Name(s): Eszopiclone
Generic Ingredient(s):

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Spectracef

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Brand Name: Spectracef
Other brand Name(s):
Generic Name(s): Cefditoren
Generic Ingredient(s):

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Ziac

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Brand Name: Ziac
Other brand Name(s):
Generic Name(s):
Generic Ingredient(s): Bisoprolol, Hydrochlorothiazide, HCTZ

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Cymbalta

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Brand Name: Cymbalta
Other brand Name(s):
Generic Name(s): Duloxetine
Generic Ingredient(s):

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Prozac

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Brand Name: Prozac
Other brand Name(s): Sarafem
Generic Name(s): Fluoxetine hydrochloride
Generic Ingredient(s):

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Patient Information Sheet from the US Food and Drug Administration

Fluoxetine hydrochloride (marketed as Prozac)

This is a summary of the most important information about fluoxetine. For details, talk to your healthcare professional.


FDA ALERT [07/2006] – Possible Life- Threatening Serotonin Syndrome When Used With Triptan Medicines

A life-threatening condition called serotonin syndrome can happen when medicines called selective serotonin reuptake inhibitors (SSRIs), such as Prozac, and medicines used to treat migraine headaches known as 5-hydroxytryptamine receptor agonists (triptans), are used together. Signs and symptoms of serotonin syndrome include the following:

  • restlessness
  • hallucinations
  • loss of coordination
  • fast heart beat
  • increased body temperature
  • fast changes in blood pressure
  • overactive reflexes
  • diarrhea
  • coma
  • nausea
  • vomiting

Serotonin syndrome may be more likely to occur when starting or increasing the dose of an SSRI or a triptan. This information comes from reports sent to FDA and knowledge of how these medicines work. If you take migraine headache medicines, ask your healthcare professional if your medicine is a triptan.

Before you take Prozac and a triptan together, talk to your healthcare professional. If you must take these medicines together, be aware of the possibility of serotonin syndrome, and get medical care right away if you think serotonin syndrome is happening to you.

This information reflects FDA’s current analysis of data available to FDA concerning this drug. FDA intends to update this sheet when additional information or analyses become available.


FDA ALERT [07/2006] – Infant Persistent Pulmonary Hypertension
The results of a study that looked at the use of antidepressant medicines during pregnancy in mothers of babies born with a serious condition called persistent pulmonary hypertension of the newborn (PPHN) were recently published in a medical journal.
Babies born with PPHN have abnormal blood flow through the heart and lungs and do not get enough oxygen to their bodies. Babies with PPHN can be very sick and may die.

The study results showed that:

  • babies born to mothers who took selective serotonin reuptake inhibitors (SSRIs), the family of medicines Prozac belongs to,
  • 20 weeks or later in their pregnancies,
  • had a higher chance (were 6 times as likely) to have persistent pulmonary hypertension (PPHN),
  • than babies born to mothers who did not take antidepressants during pregnancy.

The FDA plans to further look at the role of SSRIs in babies with PPHN.

Talk to your doctor if you are taking Prozac and are pregnant or are planning to have a baby. You and your doctor will need to talk about the best way to treat your depression during pregnancy.

This information reflects FDA’s current analysis of data available to FDA concerning this drug. FDA intends to update this sheet when additional information or analyses become available.


What is Prozac?

Prozac is in a class of medicines called selective serotonin reuptake inhibitors (SSRIs). Prozac is used to treat Depression, Obsessive-Compulsive Disorder (OCD), Bulemia Nervosa, and Panic Disorder.

Who Should Not Take Prozac?

Never take Prozac if you are taking another drug used to treat depression, called a Monoamine Oxidase Inhibitor (MAOI), or if you have stopped taking an MAOI in the last 14 days. Taking Prozac close in time to an MAOI can result in serious, sometimes fatal, reactions, including:

  • High body temperature
  • Coma
  • Seizures (convulsions)

Do not take a MAOI within 5 weeks of stopping Prozac. MAOI drugs include Nardil (phenelzine sulfate), Parnate (tranylcypromine sulfate), Marplan (isocarboxazid), and other brands.

Never take Prozac if you are taking Mellaril (thioridazine), used to treat schizophrenia. Also, do not take Mellaril within 5 weeks of stopping Prozac. Taking Prozac close in time to Mellaril can result in serious heart beat problems.

What Are The Risks?

The following are the major potential risks and side ffects of Prozac therapy. However, this list is not complete.

  • Possible life-threatening serotonin syndrome when used with triptan medicines: See FDA Alert [07/2006] above.
  • Infant persistent pulmonary hypertension: See FDA Alert [07/2006] above.
  • Suicidal thoughts or actions: Persons taking Prozac may be more likely to think about killing themselves or actually try to do so, especially when Prozac is first started or the dose is changed. People close to persons taking Prozac can help by paying attention to changes in user’s moods or actions. Contact your healthcare professional right away if someone using Prozac talks about or shows signs of killing him or herself. If you are taking Prozac yourself and you start thinking about killing yourself, tell your healthcare professional about this side effect right away.
  • Stopping Prozac: Do not stop taking Prozac suddenly because you could get side effects. Your healthcare professional will slowly decrease your dose.
  • Rash and possible allergic reactions: Prozac may cause serious skin, lung and allergic-type reactions. Contact your healthcare professional right away if you get a skin rash or hives, have problems breathing, or get swelling of your tongue, lips, or throat.
  • Bleeding problems: Prozac may cause bleeding problems, especially if taken with aspirin, NSAIDs (nonsteroidal anti-inflammatory drugs, such as ibuprofen and naproxen), or other drugs that affect bleeding.
  • Mania: You may become unusually hyperactive, excitable or elated.
  • Seizures: You may experience a seizure (convulsion), even if you are not taking Prozac close in time with an MAOI.
  • Weight loss: Prozac can cause weight loss. Children who take it for a long time should have their growth and body weight measured regularly.
  • Pregnancy: Tell your healthcare professional if you are or may be pregnant (see FDA Alert [07/2006] above). In addition to the issue described in the alert, babies delivered to mothers taking Prozac late in pregnancy have developed problems, such as difficulty breathing and feeding.
  • Sexual problems: You may have problems with impotence (erectile dysfunction), abnormal ejaculation, difficulty reaching orgasm, or decreased libido (sexual desire).
  • Other side effects include nausea, difficulty sleeping, anxiety, nervousness, and sleepiness.
  • Tell your healthcare professional about all your medical conditions, especially if you have liver or heart disease, or diabetes. Tell your healthcare professional if you are breast-feeding or plan to breast-feed your baby.

Are There Any Interactions With Drugs or Foods?

  • Do not take Prozac with Sarafem (Prozac hydrochloride), a drug used to treat PreMenstrual Dysphoric Disorder (PMDD), because they are very similar and you could get an overdose.
  • Prozac may interact with medicines other than the ones already mentioned in this information sheet, causing serious side effects. Tell your healthcare professional about all medicines, vitamins, and herbal supplements you take, especially:
    • Those that affect bleeding
    • Those used to treat diabetes, seizures, anxiety, mental illness, or depression
  • If you plan to drink alcohol, talk to your healthcare professional.

How Do I Take Prozac?

  • Prozac is taken by mouth, with or without food, exactly as prescribed by your healthcare professional.
  • Take the weekly version of Prozac only once a week. Do not start until 7 days after you’ve taken the last dose of the daily Prozac.

Is There Anything Else I need to Know?

You can get more information about antidepressants at: http://www.fda.gov/cder/drug/antidepressants/default.htm

Strattera

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Brand Name: Strattera
Other brand Name(s):
Generic Name(s): Atomoxetine
Generic Ingredient(s):

Additional Information Sources

Information Source
Consumer Health Info Eckerd Drug Advisor

 

Patient Information Sheet from the US Food and Drug Administration

Atomoxetine (marketed as Strattera)

 

This is a summary of the most important information about Strattera. For more information, talk to your healthcare professional.


FDA ALERT [09/2005] Suicidal Thinking in Children and Teens

  • Strattera may increase thoughts of suicide or suicide attempts in children and teens.
  • Call your child’s healthcare professional right away if your child or teen has:
    • new or increased thoughts of suicide
    • changes in mood or behavior including becoming irritable or anxious

The label for Strattera is being revised to include the above warnings.

This information reflects FDA’s current analysis of data available to FDA concerning this drug. FDA intends to update this sheet when additional information or analyses become available.


What Is Strattera?

Strattera is used to treat a condition called Attention-Deficit with Hyperactivity Disorder (ADHD) in children, teens, and adults. Strattera has not been studied in children under 6 years old.

Who Should Not Take Strattera?

You should not take Strattera if you:

  • are taking a medicine called a Monoamine Oxidase Inhibitor (MAOI). Do not take Strattera for at least 2 weeks after you stop taking a MAOI. Do not take a MAOI for at least 2 weeks after you stop taking Strattera.

  • have an eye disease called narrow angle glaucoma

What Are The Risks?

The following are the major potential risks and side effects of Strattera. However, this list is not complete.

The following are the major potential risks and side effects of Strattera therapy:

  • Suicidal thoughts or actions: Strattera may increase thoughts of suicide or suicide attempts in infrequent cases. Call you doctor right away if you become irritable or anxious or have other mood changes, or if you have thoughts of suicide.
  • Liver Damage: Strattera can cause liver damage in rare cases. Call your doctor right away if you have itching, dark urine, yellow skin or eyes, upper right-sided stomach area pain, or unexplained “flu-like” symptoms.
  • Weight Loss/Slowed Growth: Some people may lose weight while being treated with Strattera. It is not known if growth will be slowed in children who use Strattera for a long time. Height and weight should be watched in children who are taking Strattera.
  • Impaired Motor Skills: Do not drive or operate dangerous machines until you know how Strattera affects you.

Some common side effects that may occur with Strattera in children include:

  • upset stomach
  • decreased appetite
  • nausea or vomiting
  • dizziness
  • tiredness
  • mood swings

Some common side effects that may occur with Strattera in adults include:

  • constipation
  • dry mouth
  • nausea
  • decreased appetite
  • dizziness
  • problems sleeping
  • sexual side effects
  • problems urinating
  • menstrual cramps

These are not all of the side effects reported with Strattera. Your healthcare professional can give you a more complete list of side effects.

What Should I Tell My Healthcare Professional?

Before you start taking Strattera, tell your healthcare professional if you:

  • have or had liver problems. You may need a lower dose of Stattera.
  • have high blood pressure. Strattera can increase blood pressure.
  • have problems with your heart or an irregular heartbeat. Strattera can increase heart rate (pulse).
  • have low blood pressure. Strattera can cause dizziness or fainting in people with low blood pressure.
  • are trying to become pregnant, are already pregnant, or are breast-feeding.
  • have a problem with depression or suicidal thinking.

Can other Medicines or Food Affect Strattera?

Strattera and certain other medicines can interact with each other. Tell your healthcare professional about all the medicines you take including prescription and non-prescription medicines, vitamins, and herbal supplements. Some medicines may affect how Strattera works or Strattera may affect how your other medicines work. Know the medicines you take. Keep a list of them with you to show your healthcare professional.

Date created: September 29, 2005

Protonix

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Brand Name: Protonix
Other brand Name(s):
Generic Name(s): Pantoprazole sodium
Generic Ingredient(s):

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Cortef

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Brand Name: Cortef
Other brand Name(s): Hydrocortone
Generic Name(s): Hydrocortisone
Generic Ingredient(s):

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Advisor

Pamelor

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Brand Name: Pamelor
Other brand Name(s): Aventyl
Generic Name(s): Nortriptyline hydrochloride
Generic Ingredient(s):

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Consumer Health Info PDRHealth


Betapace

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Brand Name: Betapace
Other brand Name(s): Betapace AF
Generic Name(s): Sotalol
Generic Ingredient(s):

Additional Information Sources

Information Source
Consumer Health Info Eckerd Drug
Advisor

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