Saturday, March 10, 2012

Nasalcrom Child nasal


Generic Name: cromolyn sodium (nasal) (KRO mo lin SO dee um)

Brand Names: Nasalcrom, Nasalcrom Child


What is Nasalcrom Child (cromolyn sodium (nasal))?

Cromolyn sodium is an anti-inflammatory medication. It works by preventing the release of substances in the body that cause inflammation.


Cromolyn sodium nasal is used to prevent allergy symptoms such as runny nose, stuffy nose, sneezing, itching, and post-nasal drip.


Cromolyn sodium nasal will not treat allergy symptoms that have already begun. The medication works best if used at least 1 week before you come into contact with things you are allergic to (pollen, dust, pets, etc).


Cromolyn sodium nasal will not treat the symptoms of asthma, sinus infections, or the common cold.


Cromolyn sodium nasal may also be used for other purposes not listed in this medication guide.


What is the most important information I should know about Nasalcrom Child (cromolyn sodium (nasal))?


You should not use this medication if you are allergic to cromolyn sodium.

Before you use cromolyn sodium nasal, tell your doctor if you have asthma, drug allergies, or polyps in your nose.


Cromolyn sodium nasal will not treat allergy symptoms that have already begun. The medication works best if used at least 1 week before you come into contact with things you are allergic to (pollen, dust, pets, etc).


Stop using this medication and call your doctor if you have severe burning, stinging, or irritation in your nose, nosebleeds, sinus pain, sores in your nose, wheezing, chest tightness, fever, or green/yellow mucus from your nose.


Do not use cromolyn sodium nasal more than 6 times in a 24-hour period. Do not use this medication for longer than 12 weeks unless your doctor has told you to.

What should I discuss with my healthcare provider before using Nasalcrom Child (cromolyn sodium (nasal))?


You should not use this medication if you are allergic to cromolyn sodium.

If you have certain conditions, you may need a dose adjustment or special tests to safely use this medication. Before you use cromolyn sodium nasal, tell your doctor if you have:



  • asthma;




  • drug allergies; or




  • polyps in your nose.




FDA pregnancy category B. This medication is not expected to be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. It is not known whether cromolyn sodium passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

How should I use Nasalcrom Child (cromolyn sodium (nasal))?


Use this medication exactly as it was prescribed for you. Do not use the medication in larger amounts, or use it for longer than recommended by your doctor. Follow the directions on your prescription label.


This medicine is usually given as 1 spray into each nostril every 4 to 6 hours during allergy season or within 1 week before you will be exposed to an allergen. Follow your doctor's instructions.


Do not use cromolyn sodium nasal more than 6 times in a 24-hour period. Do not use this medication for longer than 12 weeks unless your doctor has told you to.

To use the nasal spray:



  • Blow your nose gently before each use.




  • Keeping your head upright, insert just the tip of the spray bottle into your nostril. Hold your other nostril closed with one finger. Spray the medicine into the nostril while inhaling, then sniff deeply a few times to make sure the medicine gets up into your nasal passages.




  • Repeat these steps in your other nostril.




  • After using the nasal spray, rinse the tip with hot water or wipe it with a clean tissue and recap. Avoid getting water into the nasal spray tip.



It may take up to 2 weeks of using this medicine before you get the full effect. For best results, keep using the medication as directed. Talk with your doctor if your symptoms do not improve after 2 weeks of treatment.


Store cromolyn sodium at room temperature away from moisture, heat, and light. Keep the bottle capped when not in use.

What happens if I miss a dose?


Use the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and use the medicine at the next regularly scheduled time. Do not use extra medicine to make up the missed dose.


What happens if I overdose?


Seek emergency medical attention if you think you have used too much of this medicine.

What should I avoid while using Nasalcrom Child (cromolyn sodium (nasal))?


Avoid getting this medication in your eyes. If this does happen, rinse with water.

Nasalcrom Child (cromolyn sodium (nasal)) side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives or itching; difficulty breathing; severe dizziness; swelling of your face, lips, tongue, or throat.

Stop using this medication and call your doctor if you have any of these serious side effects:



  • severe burning, stinging, or irritation in your nose;




  • nosebleeds, sinus pain, or sores in your nose;




  • wheezing, tight feeling in your chest; or




  • fever, green or yellow mucus from the nose.




Less serious side effects may include mild burning or stinging inside your nose after use.

This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088.


What other drugs will affect Nasalcrom Child (cromolyn sodium (nasal))?


There may be other drugs that can interact with cromolyn sodium nasal. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.



More Nasalcrom Child resources


  • Nasalcrom Child Side Effects (in more detail)
  • Nasalcrom Child Use in Pregnancy & Breastfeeding
  • 0 Reviews for Nasalcrom Child - Add your own review/rating


Compare Nasalcrom Child with other medications


  • Hay Fever


Where can I get more information?


  • Your pharmacist can provide more information about cromolyn sodium nasal.

See also: Nasalcrom Child side effects (in more detail)


Friday, March 9, 2012

gonadorelin injectable


Generic Name: gonadorelin (injectable) (gon ah doe REH lin)

Brand names: Factrel, Lutrepulse


What is gonadorelin?

Gonadorelin is a man-made protein that is like a hormone in the body called gonadotropin-releasing hormone (GnRH). GnRH causes the pituitary gland to release other hormones including luteinizing hormone (LH) and follicle-stimulating hormone (FSH). LH and FSH are important for proper development in children and fertility in adults.


Gonadorelin is used to test how well the hypothalamus and pituitary glands are working.


Gonadorelin may also be used for purposes other than those listed in this medication guide.


What is the most important information I should know about gonadorelin?


Before using gonadorelin, tell your doctor if you have any other medical conditions or if you take any medications, including herbal products. You may not be able to take gonadorelin, or you may require a dosage adjustment or special monitoring.


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


Before using gonadorelin, tell your doctor if you have any other medical conditions or if you take any medications, including herbal products. You may not be able to take gonadorelin, or you may require a dosage adjustment or special monitoring.


Gonadorelin is in the FDA pregnancy category B. This means that it is not expected to be harmful to an unborn baby. Do not take gonadorelin without first talking to your doctor if you are pregnant. It is not known whether gonadorelin passes into breast milk. Do not take gonadorelin without first talking to your doctor if you are breast-feeding a baby.

How should I take gonadorelin?


Gonadorelin is administered by a healthcare professional as a subcutaneous (under the skin) or intravenous (into a vein) injection.


Blood samples will be drawn before and after administration of gonadorelin to measure hormone levels in the body.


Your healthcare provider will store gonadorelin as directed by the manufacturer. If you are storing gonadorelin at home, your healthcare provider will provide storage instructions.


What happens if I miss a dose?


Missing a dose of gonadorelin should not occur as it is used for testing purposes only.


What happens if I overdose?


An overdose of gonadorelin is unlikely to threaten life. Notify your doctor immediately or call an emergency room or poison control center for advice if an overdose is suspected.

Symptoms of a gonadorelin overdose are not known.


What should I avoid while taking gonadorelin?


There are no restrictions on food, beverages, or activity during treatment with gonadorelin unless otherwise directed by your doctor.


Gonadorelin side effects


If you experience a rare allergic reaction (difficulty breathing; closing of the throat; swelling of the lips, tongue, or face; or hives) to gonadorelin, seek emergency medical attention.

Other less serious side effects may also occur. Notify your doctor if you experience



  • headache;




  • flushing;




  • nausea or abdominal discomfort;




  • dizziness or lightheadedness;




  • pain, swelling, or itching at the injection site; or




  • skin rash.



Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.


Gonadorelin Dosing Information


Usual Adult Dose for Gonadotropin Deficiency:

0.1 mg injected once subcutaneously or intravenously as a single dose.

Usual Adult Dose for Amenorrhea:

5 mcg every 90 minutes (range of 1 to 20 mcg) delivered intravenously by a pump over 1 minute, every ninety minutes for 21 days.


What other drugs will affect gonadorelin?


Other medicines that affect hormone levels in the body may affect test results following treatment with gonadorelin. Talk to your doctor and pharmacist before taking any prescription or over-the-counter medicines, including herbal products during treatment with gonadorelin.



More gonadorelin resources


  • Gonadorelin Side Effects (in more detail)
  • Gonadorelin Use in Pregnancy & Breastfeeding
  • Gonadorelin Drug Interactions
  • Gonadorelin Support Group
  • 0 Reviews for Gonadorelin - Add your own review/rating


Compare gonadorelin with other medications


  • Amenorrhea
  • Gonadotropin Deficiency


Where can I get more information?


  • Your pharmacist has additional information about gonadorelin written for health professionals that you may read.

What does my medication look like?


Gonadorelin is available with a prescription under the brand name Factrel. Other brand or generic formulations may also be available. Ask your pharmacist any questions you have about this medication, especially if it is new to you.


See also: gonadorelin side effects (in more detail)


nitroglycerin transdermal



Generic Name: nitroglycerin (transdermal) (NYE troe GLIS er in)

Brand Names: Minitran, Nitrek, Nitro TD Patch-A, Nitro-Dur


What is nitroglycerin transdermal?

Nitroglycerin is in a group of drugs called nitrates. Nitroglycerin dilates (widens) blood vessels, making it easier for blood to flow through them and easier for the heart to pump.


Nitroglycerin transdermal is used to prevent attacks of chest pain (angina).


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


What is the most important information I should know about nitroglycerin transdermal?


You should not use this medication if you are allergic to nitroglycerin, isosorbide mononitrate (Imdur), or isosorbide dinitrate (BiDil, Isordil).

Before using nitroglycerin transdermal, tell your doctor if you have congestive heart failure, low blood pressure, glaucoma, anemia, or a history of heart attack, stroke, or head injury.


Do not use this medication to treat an angina attack that has already begun. It will not work fast enough.

Nitroglycerin transdermal can cause severe headaches, especially when you first start using it. Do not stop using the skin patches, and ask your doctor before using any headache pain medication.


Nitroglycerin may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert. Call your doctor at once if you have a serious side effect such as worsening chest pain, pain spreading to the arm or shoulder, nausea, vomiting, sweating, blurred vision and dry mouth, or fainting. Drinking alcohol can increase certain side effects of nitroglycerin. The nitroglycerin transdermal patch may burn your skin if you wear the patch during an MRI (magnetic resonance imaging). Remove the patch before undergoing such a test.

What should I discuss with my healthcare provider before using nitroglycerin transdermal?


You should not use this medication if you are allergic to nitroglycerin, isosorbide mononitrate (Imdur), or isosorbide dinitrate (BiDil, Isordil). Do not use nitroglycerin transdermal if you are allergic to any type of adhesive on a bandage or other transdermal skin patch.

To make sure you can safely use nitroglycerin, tell your doctor if you have any of these other conditions:



  • congestive heart failure;




  • a history of heart attack, stroke, or head injury;




  • low blood pressure;




  • glaucoma; or




  • anemia (lack of red blood cells).




FDA pregnancy category C. It is not known whether nitroglycerin will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. It is not known whether nitroglycerin transdermal passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

How should I use nitroglycerin transdermal?


Use exactly as prescribed by your doctor. Do not use in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label.


Do not use nitroglycerin transdermal to treat an angina attack that has already begun. It will not work fast enough. Your doctor may prescribe an oral form of nitroglycerin (tablet, capsule, spray) to treat an angina attack. Talk with your doctor if any of your medications do not seem to work as well in treating or preventing angina attacks.

The nitroglycerin transdermal skin patch is usually worn for 12 to 14 hours and then removed. A new patch is put on after a "patch-free" period of 10 to 12 hours. Your doctor may want you to wear the patch for longer or shorter periods of time. Follow your doctor's instructions carefully.


Apply the skin patch to a clean, dry, hairless area of the body, below your neck and above your knees or elbows. To remove any hair from these skin areas, clip the hair short but do not shave it.


Press the patch onto the skin and press it down firmly with your fingers. Make sure it is well sealed around the edges.


Wash your hands after applying a nitroglycerin transdermal skin patch.

If the patch falls off, try sticking it back on. If you replace the patch with a new one, leave it on only for the rest of your wearing time. Do not change your patch removal schedule.


After removing a skin patch fold it in half, sticky side in, and throw it away in a place where children or pets cannot get to it. Keep both used and unused nitroglycerin skin patches out of the reach of children or pets. Do not stop using this medication without your doctor's advice, even if you feel better. You may have increased angina attacks if you stop using the medication suddenly.

If you need to have any type of surgery or dental work, tell the surgeon or dentist ahead of time that you are using nitroglycerin transdermal.


The nitroglycerin transdermal patch may burn your skin if you wear the patch during an MRI (magnetic resonance imaging). Remove the patch before undergoing such a test.

Tell any doctor or other healthcare provider who treats you that you are using nitroglycerin transdermal. If you need emergency heart resuscitation, your family or caregivers should tell emergency medical personnel if you are wearing a nitroglycerin skin patch. The patch should be removed before any electrical equipment (such as a defribrillator) is used on you.


Store at room temperature, away from moisture and heat. Keep each skin patch in its sealed pouch until you are ready to use it.

What happens if I miss a dose?


Apply a patch as soon as you remember, and keep it on for the rest of your wearing time without changing your patch removal schedule. If you miss a dose and it is almost time to apply your next patch, wait until then to apply the patch and skip the missed dose.


Do not use extra patches to make up a 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 a severe throbbing headache, confusion, fever, fast or pounding heartbeats, dizziness, vision problems, nausea, vomiting, bloody diarrhea, trouble breathing, cold or clammy skin, feeling light-headed, fainting, seizure (convulsions), or blue-colored skin, lips, or nails.


What should I avoid while using nitroglycerin transdermal?


Avoid using nitroglycerin transdermal on irritated or broken skin.


Nitroglycerin may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.

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.


Drinking alcohol can increase certain side effects of nitroglycerin.

Nitroglycerin transdermal side effects


Nitroglycerin transdermal can cause severe headaches, especially when you first start using it. These headaches may gradually become less severe as you continue to use nitroglycerin transdermal. Do not stop using the medication. Ask your doctor before using any headache pain medication.


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Call your doctor at once if you have a serious side effect such as:

  • worsening chest pain, slow heart rate;




  • feeling like you might pass out;




  • chest pain or heavy feeling, pain spreading to the arm or shoulder, nausea, sweating, general ill feeling;




  • fast or pounding heartbeats; or




  • blurred vision and dry mouth.



Less serious side effects may include:



  • mild skin rash or itching;




  • warmth, redness, or tingly feeling under your skin;




  • nausea, vomiting, upset stomach; or




  • feeling nervous, weak, or dizzy.



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.


Nitroglycerin Dosing Information


Usual Adult Dose for Angina Pectoris:

For relief of acute anginal attack:

Lingual spray: 1 to 2 sprays (0.4 to 0.8 mg) onto or under the tongue every 3 to 5 minutes as needed, up to 3 sprays in 15 minutes. If pain persists after the maximum number of doses, prompt medical attention is recommended.

Sublingual tablet: 0.3 to 0.6 mg dissolved under the tongue or in the buccal pouch every 5 minutes as needed, up to 3 doses in 15 minutes. If pain persists after the maximum number of doses, prompt medical attention is recommended.

IV continuous infusion (via non PVC tubing): 5 mcg/min initially, increased by 5 mcg/min every 3 to 5 minutes as needed up to 20 mcg/min, then gradually by 10 and then 20 mcg/min if needed, up to a usual maximum of 200 and generally no more than 400 mcg/min. Starting dosages of 25 mcg/min or higher have been used with PVC administration sets.

Usual Adult Dose for Angina Pectoris Prophylaxis:

Lingual spray: 1 to 2 sprays (0.4 to 0.8 mg) onto or under the tongue 5 to 10 minutes prior to engaging in activities which might precipitate an acute attack

Sublingual tablet: 0.3 to 0.6 mg dissolved under the tongue or in the buccal pouch 5 to 10 minutes prior to engaging in activities which might precipitate an acute attack

Topical ointment: 1/2 inch initially, applied to a non hairy area of the trunk every 6 to 8 hours during waking hours (2 times a day); titrate as needed and tolerated. If angina occurs while the ointment is in place, the dose should be increased; if angina occurs several hours after application, the dosing frequency should be increased. Usual range is 1/2 to 2 inches (7.5 to 30 mg) every 8 hours, typically applied to 36 square inches of truncal skin.

Transdermal patch: 0.1 to 0.4 mg/hr patch applied to a dry and hairless area of the upper arm or body for 12 to 14 hours per day; titrate as needed and tolerated up to 0.8 mg/hr. Application sites should be rotated to avoid skin irritation.

Transmucosal (buccal) tablet: 1 mg dissolved between the lip and gum above the upper incisors or between the cheek and gum every 3 to 5 hours during waking hours (approximately 3 times a day); titrate as needed and tolerated. If angina occurs while a tablet is in place, the dose should be increased to the next strength; if angina occurs after dissolution of tablet, the dosing frequency should be increased. Usual maintenance dosage is 2 mg three times a day. If an acute attack occurs while a tablet is in place, another tablet may be administered on the opposite side from the one already in place. Sublingual nitroglycerin is recommended if prompt relief is not attained.

Oral: 2.5 every 8 to 12 hours; titrate as needed and tolerated up to 9 mg every 8 to 12 hours

Because tolerance to nitroglycerin may develop if plasma levels are maintained continuously, a nitrate free interval of 10 to 12 hours per day may be appropriate during chronic prophylaxis of angina pectoris. However, clinical studies suggest that such intermittent use may be associated with hemodynamic rebound during drug withdrawal and decreased exercise tolerance during the latter part of the nitrate free interval. Although the clinical relevance of this observation is unknown, a potentially increased risk of anginal attack during the nitrate free interval should be considered. Therefore, dosing regimens should be carefully individualized to each patient. Other antianginal drugs such as beta-blockers and calcium channel blockers may be prescribed to reduce the risk of aggravating myocardial ischemia during the drug free intervals.

Usual Adult Dose for Congestive Heart Failure:

Topical ointment: 1/2 inch initially, applied to a non hairy area of the trunk every 6 to 8 hours during waking hours (2 times a day); titrate as needed and tolerated. Usual range is 1/2 to 2 inches (7.5 to 30 mg) every 8 hours, typically applied to 36 square inches of truncal skin.

Transdermal patch: 0.1 to 0.4 mg/hr patch applied to a dry and hairless area of the upper arm or body for 12 to 14 hours per day; titrate as needed and tolerated up to 0.8 mg/hr. Application sites should be rotated to avoid skin irritation.

Transmucosal (buccal) tablet: 1 mg dissolved between the lip and gum above the upper incisors or between the cheek and gum every 3 to 5 hours during waking hours (approximately 3 times a day); titrate as needed and tolerated. Usual maintenance dosage is 2 mg three times a day.

Oral: 2.5 every 8 to 12 hours; titrate as needed and tolerated up to 9 mg every 8 to 12 hours

Usual Adult Dose for Myocardial Infarction:

For the initial 24 to 48 hours after an acute myocardial infarction:

IV continuous infusion (via non PVC tubing): 5 mcg/min initially, increased by 5 mcg/min every 3 to 5 minutes as needed up to 20 mcg/min, then gradually by 10 and then 20 mcg/min if needed up to a usual maximum of 200 and generally no more than 400 mcg/min. Starting dosages of 25 mcg/min or higher have been used with PVC administration sets.

Usual Adult Dose for Hypertension:

IV continuous infusion (via non PVC tubing): 5 mcg/min initially, increased by 5 mcg/min every 3 to 5 minutes as needed up to 20 mcg/min, then gradually by 10 and then 20 mcg/min if needed up to a usual maximum of 100 mcg/min. Starting dosages of 25 mcg/min or higher have been used with PVC administration sets.

Usual Adult Dose for Anal Fissure and Fistula:

For the treatment of moderate to severe pain associated with chronic anal fissure:
Apply 1 inch of ointment (375 mg of ointment equivalent to 1.5 mg of nitroglycerin) intra anally every 12 hours for up to 3 weeks.

Usual Pediatric Dose for Hypertension:

Perioperative hypertension or induction of intraoperative hypotension:

IV continuous infusion: 0.25 to 0.5 mcg/kg/min initially, increase by 0.5 to 1 mcg/kg/min every 3 to 5 minutes as needed up to 5 mcg/kg/min. Usual dose is 1 to 3 mcg/kg/min, but doses as high as 20 mcg/kg/min have been used.


What other drugs will affect nitroglycerin transdermal?


Tell your doctor about all other medications you use, especially:



  • blood pressure medication or diuretics (water pills);




  • cold or allergy medicines, diet pills, or over-the-counter pain medicine such as ibuprofen (Advil, Motrin) or naproxen (Aleve);




  • an erectile dysfunction medication such as sildenafil (Viagra), tadalafil (Cialis), or vardenafil (Levitra);




  • migraine headache medication such as ergotamine (Ergomar, Cafergot, Migergot), dihydroergotamine (D.H.E. 45, Migranal), or methylergonovine (Methergine);




  • a beta-blocker such as atenolol (Tenormin, Tenoretic), carvedilol (Coreg), labetalol (Normodyne, Trandate), metoprolol (Dutoprol, Lopressor, Toprol), nadolol (Corgard), propranolol (Inderal, InnoPran), sotalol (Betapace), and others; or




  • heart or blood pressure medicine such as amlodipine (Norvasc, Caduet, Exforge, Lotrel, Tekamlo, Tribenzor, Twynsta), diltiazem (Cartia, Cardizem), nifedipine (Nifedical, Procardia), verapamil (Calan, Covera, Isoptin, Verelan), and others.



This list is not complete and other drugs may interact with nitroglycerin. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.



More nitroglycerin resources


  • Nitroglycerin Side Effects (in more detail)
  • Nitroglycerin Dosage
  • Nitroglycerin Use in Pregnancy & Breastfeeding
  • Drug Images
  • Nitroglycerin Drug Interactions
  • Nitroglycerin Support Group
  • 6 Reviews for Nitroglycerin - Add your own review/rating


Compare nitroglycerin with other medications


  • Anal Fissure and Fistula
  • Angina
  • Angina Pectoris Prophylaxis
  • Heart Attack
  • Heart Failure
  • High Blood Pressure
  • Raynaud's Syndrome


Where can I get more information?


  • Your pharmacist can provide more information about nitroglycerin transdermal.

See also: nitroglycerin side effects (in more detail)


Thursday, March 8, 2012

Thera-Tabs


Generic Name: Multivitamins (MUL-ti-VYE-ta-mins)
Brand Name: Examples include Stress-600 and Thera-Tabs


Thera-Tabs is used for:

Treating or preventing low levels of vitamins in the body. It may also be used for other conditions as determined by your doctor.


Thera-Tabs is a vitamin supplement. It works by providing extra vitamins to the body.


Do NOT use Thera-Tabs if:


  • you are allergic to any ingredient in Thera-Tabs

Contact your doctor or health care provider right away if any of these apply to you.



Before using Thera-Tabs:


Some medical conditions may interact with Thera-Tabs. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


  • if you are pregnant, planning to become pregnant, or are breast-feeding

  • if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

  • if you have allergies to medicines, foods, or other substances

Some MEDICINES MAY INTERACT with Thera-Tabs.


Ask your health care provider if Thera-Tabs may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.


How to use Thera-Tabs:


Use Thera-Tabs as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Take Thera-Tabs by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.

  • If you miss a dose of Thera-Tabs, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Thera-Tabs.



Important safety information:


  • Do not take large doses of vitamins while you use Thera-Tabs unless your doctor tells you to.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Thera-Tabs while you are pregnant. It is not known if Thera-Tabs is found in breast milk. If you are or will be breast-feeding while you use Thera-Tabs, check with your doctor. Discuss any possible risks to your baby.


Possible side effects of Thera-Tabs:


All medicines may cause side effects, but many people have no, or minor, side effects. No COMMON side effects have been reported with Thera-Tabs. Seek medical attention right away if any of these SEVERE side effects occur:



Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue).



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.


See also: Thera-Tabs side effects (in more detail)


If OVERDOSE is suspected:


Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center, or emergency room immediately. Symptoms may include nausea; vomiting.


Proper storage of Thera-Tabs:

Store Thera-Tabs at room temperature. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Thera-Tabs out of the reach of children and away from pets.


General information:


  • If you have any questions about Thera-Tabs, please talk with your doctor, pharmacist, or other health care provider.

  • Thera-Tabs is to be used only by the patient for whom it is prescribed. Do not share it with other people.

  • If your symptoms do not improve or if they become worse, check with your doctor.

This information is a summary only. It does not contain all information about Thera-Tabs. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Thera-Tabs resources


  • Thera-Tabs Side Effects (in more detail)
  • Thera-Tabs Use in Pregnancy & Breastfeeding
  • Thera-Tabs Drug Interactions
  • Thera-Tabs Support Group
  • 0 Reviews for Thera-Tabs - Add your own review/rating


Compare Thera-Tabs with other medications


  • Dietary Supplementation

Tuesday, March 6, 2012

Nitromist oral/sublingual


Generic Name: nitroglycerin (oral/sublingual) (NYE troe GLI ser in (OR al/sub LIN gwal))

Brand Names: Nitro-Time, Nitrolingual, Nitrolingual Duo Pack, Nitromist, Nitrostat


What is nitroglycerin?

Nitroglycerin is in a group of drugs called nitrates. Nitroglycerin dilates (widens) blood vessels, making it easier for blood to flow through them and easier for the heart to pump.


Nitroglycerin is used to treat or prevent attacks of chest pain (angina).


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


What is the most important information I should know about nitroglycerin?


Do not use nitroglycerin if you are taking sildenafil (Viagra, Revatio), tadalafil (Cialis), or vardenafil (Levitra). Serious, life-threatening side effects can occur if you take nitroglycerin while you are using sildenafil.

Nitroglycerin can cause severe headaches, especially when you first start using it. These headaches may gradually become less severe as you continue to use nitroglycerin. Do not stop taking the medication. Ask your doctor before using any headache pain medication.


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


Do not use nitroglycerin if you are taking sildenafil (Viagra, Revatio), tadalafil (Cialis), or vardenafil (Levitra). Serious, life-threatening side effects can occur if you take nitroglycerin while you are using sildenafil.

Do not use this medication without the advice of a doctor if you have early signs of a heart attack (chest pain or heavy feeling, pain spreading to the arm or shoulder, nausea, sweating, general ill feeling). Seek emergency medical attention if you have symptoms of a heart attack.


You should not use this medication if you are allergic to nitroglycerin or other nitrates such as isosorbide dinitrate (Dilatrate, Isordil, Isochron) or isosorbide mononitrate (Imdur, ISMO, Monoket), or if you have:

  • severe anemia (a lack of red blood cells); or




  • a brain injury, hemorrhage, or tumor.



To make sure you can safely take nitroglycerin, tell your doctor if you have any of these other conditions:



  • congestive heart failure;




  • a history of heart attack, stroke, or head injury;




  • low blood pressure;




  • glaucoma;




  • migraine headaches; or



  • liver disease.


FDA pregnancy category C. It is not known whether nitroglycerin will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. It is not known whether nitroglycerin passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

Nitroglycerin can cause severe headaches, especially when you first start using it. These headaches may gradually become less severe as you continue to use nitroglycerin. Do not stop taking the medication. Ask your doctor before using any headache pain medication.


How should I take nitroglycerin?


Take exactly as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label.


If possible, try to rest or stay seated when you use this medication. Nitroglycerin can cause dizziness or fainting.


If you use nitroglycerin sublingual spray to treat an angina attack: At the first sign of an attack, apply the spray directly on or under your tongue. Close your mouth after each spray. Do not inhale the spray. Do not shake the spray before or during use. You may use additional sprays every 5 minutes, but not more than 3 sprays in 15 minutes.


You may use nitroglycerin spray within 5 to 10 minutes before an activity you think might cause chest pain. Follow your doctor's instructions.


The nitroglycerin sublingual tablet should be placed under your tongue and allowed to dissolve slowly. Do not chew or swallow it. You may use additional tablets every 5 minutes, but not more than 3 tablets in 15 minutes.


Seek emergency medical attention if your chest pain gets worse or lasts more than 5 minutes, especially if you have trouble breathing or feel weak, dizzy, or nauseated, or lightheaded. You may feel a slight burning or stinging in your mouth when you use this medication. However, this sensation is not a sign of how well the medication is working. Do not use more medication just because you do not feel a burning or stinging. Do not crush, chew, break, or open an extended-release capsule. Swallow the pill whole. It is specially made to release medicine slowly in the body. Breaking or opening the pill would cause too much of the drug to be released at one time.

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


Keep this medicine on hand at all times in case of an angina attack. Get your prescription refilled before you run out of medicine completely.


If you take nitroglycerin on a regular schedule to prevent angina, do not stop taking it suddenly or you could have a severe attack of angina. Store the tablets in the glass container at room temperature, away from moisture and heat. Keep the spray away from open flame or high heat, such as in a car on a hot day. The canister may explode if it gets too hot.

What happens if I miss a dose?


Since nitroglycerin is taken as needed, you may not be on a dosing schedule. If you are taking the medication regularly, take the missed dose as soon as you remember. Skip the missed dose if your next dose is less than 2 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. An overdose of nitroglycerin can be fatal.

Overdose symptoms may include a severe throbbing headache, confusion, fever, fast or pounding heartbeats, dizziness, vision problems, nausea, vomiting, bloody diarrhea, trouble breathing, cold or clammy skin, feeling light-headed, fainting, and seizures.


What should I avoid while taking nitroglycerin?


Nitroglycerin can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert. Avoid drinking alcohol. It can increase some of the side effects of nitroglycerin, such as dizziness, drowsiness, feeling light-headed, or fainting.

Nitroglycerin side effects


Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Call your doctor at once if you have a serious side effect such as:

  • fast, slow, pounding, or uneven heart rate;




  • blurred vision or dry mouth;




  • nausea, vomiting, sweating, pale skin, feeling like you might pass out; or




  • fever, sore throat, and headache with a severe blistering, peeling, and red skin rash.



Less serious side effects may include:



  • mild burning or tingling with the tablet in your mouth;




  • warmth, redness, or tingly feeling under your skin; or




  • feeling weak or dizzy.



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 nitroglycerin?


Many drugs can interact with nitroglycerin. Below is just a partial list. Tell your doctor if you are using:



  • alteplase (Activase);




  • aspirin or heparin;




  • bladder or urinary medications such as oxybutynin (Ditropan) or tolterodine (Detrol);




  • blood pressure medication;




  • bronchodilators such as ipratropium (Atrovent) or tiotropium (Spiriva);




  • dihydroergotamine (D.H.E. 45, Migranal) or ergotamine (Ergomar, Cafergot, and others);




  • an antidepressant such as amitriptyline (Elavil, Vanatrip, Limbitrol), clomipramine (Anafranil), imipramine (Tofranil), and others;




  • a beta-blocker such as atenolol (Tenormin), carvedilol (Coreg), metoprolol (Lopressor, Toprol), nadolol (Corgard), propranolol (Inderal), sotalol (Betapace), and others;




  • a calcium channel blocker such as diltiazem (Tiazac, Cardizem), nifedipine (Procardia), nimodipine (Nimotop), verapamil (Calan, Covera, Verelan), and others;




  • irritable bowel medications such as dicyclomine (Bentyl), hyoscyamine (Anaspaz, Cystospaz, and others), or propantheline (Pro-Banthine);




  • any medication that causes dry mouth; or




  • medicines to treat psychiatric disorders, such as chlorpromazine (Thorazine), haloperidol (Haldol), thioridazine (Mellaril), and others.



This list is not complete and there are many other drugs that can interact with nitroglycerin. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.



More Nitromist resources


  • Nitromist Side Effects (in more detail)
  • Nitromist Use in Pregnancy & Breastfeeding
  • Nitromist Drug Interactions
  • Nitromist Support Group
  • 0 Reviews for Nitromist - Add your own review/rating


Compare Nitromist with other medications


  • Angina
  • Angina Pectoris Prophylaxis
  • Heart Attack
  • Heart Failure
  • High Blood Pressure


Where can I get more information?


  • Your pharmacist can provide more information about nitroglycerin.

See also: Nitromist side effects (in more detail)


Sunday, March 4, 2012

pegloticase Intravenous


peg-LOE-ti-kase


Intravenous route(Solution)

Anaphylaxis and infusion reactions have been reported to occur during and after administration of pegloticase. Pegloticase should be administered in healthcare settings and by healthcare providers prepared to manage anaphylaxis and infusion reactions. Patients should be premedicated with antihistamines and corticosteroids and be closely monitored for an appropriate period of time for anaphylaxis after administration of pegloticase. Monitor serum uric acid levels prior to infusions and consider discontinuing treatment if levels increase to above 6 mg/dL, particularly when 2 consecutive levels above 6 mg/dL are observed .



Commonly used brand name(s)

In the U.S.


  • Krystexxa

Available Dosage Forms:


  • Solution

Pharmacologic Class: Enzyme


Uses For pegloticase


Pegloticase injection is used to treat chronic gout in adult patients who have already been treated with other medicines that did not work well. Gout is a condition that is caused by too much uric acid in the blood (hyperuricemia).


Pegloticase injection works by causing less uric acid to be produced by the body. pegloticase will not relieve a gout attack that has already started.


pegloticase is to be administered only by or under the immediate supervision of your doctor.


Before Using pegloticase


In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For pegloticase, the following should be considered:


Allergies


Tell your doctor if you have ever had any unusual or allergic reaction to pegloticase or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.


Pediatric


Appropriate studies have not been performed on the relationship of age to the effects of pegloticase injection in children. Safety and efficacy have not been established.


Geriatric


Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of pegloticase injection in the elderly.


Pregnancy








Pregnancy CategoryExplanation
All TrimestersCAnimal studies have shown an adverse effect and there are no adequate studies in pregnant women OR no animal studies have been conducted and there are no adequate studies in pregnant women.

Breast Feeding


There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding.


Interactions with Medicines


Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. Tell your healthcare professional if you are taking any other prescription or nonprescription (over-the-counter [OTC]) medicine.


Interactions with Food/Tobacco/Alcohol


Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco.


Other Medical Problems


The presence of other medical problems may affect the use of pegloticase. Make sure you tell your doctor if you have any other medical problems, especially:


  • Glucose-6-phosphate dehydrogenase (G6PD) deficiency (a hereditary metabolic disorder affecting red blood cells) or

  • Hyperuricemia, asymptomatic (without noticeable symptoms)—Should not be used in patients with these conditions.

  • Congestive heart failure—Use with caution. May make this condition worse.

Proper Use of pegloticase


A nurse or other trained health professional will give you pegloticase in a hospital or clinic. pegloticase is given through a needle placed in one of your veins.


pegloticase must be given slowly, so the needle will remain in place for a few hours (up to 2 hours or longer). You may also receive medicines (e.g., antihistamines, corticosteroids) to help prevent possible allergic reactions to the injection.


pegloticase is usually given every two weeks. If you miss a dose or forget to receive your medicine, call your doctor for instructions.


pegloticase should come with a Medication Guide. Read and follow the instructions carefully. Ask your doctor if you have any questions.


Precautions While Using pegloticase


Your doctor will check your progress closely while you are receiving pegloticase. This will allow your doctor to see if the medicine is working properly and to decide if you should continue to receive it. Blood tests may be needed to check for unwanted effects.


pegloticase may cause a serious type of allergic reaction called anaphylaxis. Anaphylaxis can be life-threatening and requires immediate medical attention. Call your doctor right away if you have a rash; hives; itching; dizziness; shortness of breath; swelling of your hands, face, mouth, or tongue; trouble with breathing or swallowing; or chest pain after you receive the medicine.


pegloticase may cause infusion reactions, such as a rash, itching, or redness of the skin; difficulty with breathing; feeling of warmth or redness of the face, neck, arms and occasionally, upper chest; or chest discomfort or pain, while you are receiving the injection or within 2 hours after you receive it. Stop using pegloticase and check with your doctor or nurse right away if you have any of these symptoms.


Patients of African or Mediterranean ancestry are at higher risk of serious side effects and should be carefully evaluated by their doctor before starting pegloticase.


Gout flares may occur in the first three months when you start receiving pegloticase. Do not stop receiving pegloticase even if you have a gout flare. Your doctor may give you medicines (e.g., colchicine, non-steroidal antiinflammatory drug or NSAID) to reduce and prevent worsening of the gout.


pegloticase Side Effects


Along with its needed effects, a medicine may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.


Check with your doctor or nurse immediately if any of the following side effects occur:


More common
  • Chest pain or discomfort

  • cough

  • difficult or labored breathing

  • difficulty with swallowing

  • dizziness

  • facial swelling

  • fast heartbeat

  • fever or chills

  • flushing or redness of the skin

  • gout flare

  • headache

  • hives or welts

  • itching

  • nausea or vomiting

  • puffiness or swelling of the eyelids or around the eyes, face, lips, or tongue

  • redness of the skin

  • shortness of breath

  • skin rash

  • tightness in the chest

  • unusual tiredness or weakness

  • unusually warm skin

  • wheezing

Rare
  • Decreased urine output

  • dilated neck veins

  • extreme fatigue

  • irregular breathing

  • irregular heartbeat

  • swelling of the face, fingers, feet, or lower legs

  • troubled breathing

  • weight gain

Some side effects may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects. Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:


More common
  • Bruise

  • contusion

  • difficulty having a bowel movement (stool)

  • large, flat, blue, or purplish patches in the skin

  • muscle aches

  • sore throat

  • stuffy or runny nose

Less common
  • Vomiting

Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.

See also: pegloticase Intravenous side effects (in more detail)



The information contained in the Thomson Reuters Micromedex products as delivered by Drugs.com is intended as an educational aid only. It is not intended as medical advice for individual conditions or treatment. It is not a substitute for a medical exam, nor does it replace the need for services provided by medical professionals. Talk to your doctor, nurse or pharmacist before taking any prescription or over the counter drugs (including any herbal medicines or supplements) or following any treatment or regimen. Only your doctor, nurse, or pharmacist can provide you with advice on what is safe and effective for you.


The use of the Thomson Reuters Healthcare products is at your sole risk. These products are provided "AS IS" and "as available" for use, without warranties of any kind, either express or implied. Thomson Reuters Healthcare and Drugs.com make no representation or warranty as to the accuracy, reliability, timeliness, usefulness or completeness of any of the information contained in the products. Additionally, THOMSON REUTERS HEALTHCARE MAKES NO REPRESENTATION OR WARRANTIES AS TO THE OPINIONS OR OTHER SERVICE OR DATA YOU MAY ACCESS, DOWNLOAD OR USE AS A RESULT OF USE OF THE THOMSON REUTERS HEALTHCARE PRODUCTS. ALL IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE OR USE ARE HEREBY EXCLUDED. Thomson Reuters Healthcare does not assume any responsibility or risk for your use of the Thomson Reuters Healthcare products.


More pegloticase Intravenous resources


  • Pegloticase Intravenous Side Effects (in more detail)
  • Pegloticase Intravenous Use in Pregnancy & Breastfeeding
  • Pegloticase Intravenous Drug Interactions
  • Pegloticase Intravenous Support Group
  • 2 Reviews for Pegloticase Intravenous - Add your own review/rating


Compare pegloticase Intravenous with other medications


  • Gout

Saturday, March 3, 2012

Zarontin


Generic Name: ethosuximide (ETH oh SUX i mide)

Brand Names: Zarontin


What is Zarontin (ethosuximide)?

Ethosuximide is an anti-epileptic medication, also called an anticonvulsant.


Ethosuximide is used alone or in combination with other medications to treat absence seizures (also called "petit mal" seizures) in adults and children.


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


What is the most important information I should know about Zarontin (ethosuximide)?


Ethosuximide can cause a decrease in many types of blood cells (white cells, red cells, platelets). Call your doctor at once if you have any unusual bleeding, weakness, or any signs of infection, even if these symptoms first occur after you have been using the medication for several months.

Ethosuximide may also cause liver damage. Call your doctor if you have symptoms such as loss of appetite, stomach pain, or jaundice (yellowing of the skin or eyes).


You may have thoughts about suicide while taking this medication. Your doctor will need to check you at regular visits. Do not miss any scheduled appointments.


Call your doctor at once if you have any new or worsening symptoms such as: mood or behavior changes, anxiety, depression, panic attacks, trouble sleeping, or if you feel impulsive, irritable, agitated, hostile, aggressive, restless, hyperactive (mentally or physically), or have thoughts about suicide or hurting yourself.


Do not stop using ethosuximide without first talking to your doctor, even if you feel fine. You may have increased seizures if you stop using ethosuximide suddenly. You will need to use less and less before you stop the medication completely.

Contact your doctor if your seizures get worse or you have them more often while taking ethosuximide.


Wear a medical alert tag or carry an ID card stating that you take ethosuximide. Any medical care provider who treats you should know that you take seizure medication.

What should I discuss with my healthcare provider before taking Zarontin (ethosuximide)?


You should not use this medication if you are allergic to ethosuximide or to other seizure medications.

To make sure you can safely take ethosuximide, tell your doctor if you have any of these other conditions:



  • lupus;




  • liver disease;




  • kidney disease; or




  • a history of depression, mood problems, or suicidal thoughts or actions.



You may have thoughts about suicide while taking this medication. Tell your doctor if you have new or worsening depression or suicidal thoughts during the first several months of treatment, or whenever your dose is changed.


Your family or other caregivers should also be alert to changes in your mood or symptoms. Your doctor will need to check you at regular visits. Do not miss any scheduled appointments.


It is not known whether ethosuximide is harmful to an unborn baby, but having a seizure during pregnancy could harm both mother and baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. Follow your doctor's instructions about taking ethosuximide while you are pregnant. If you are pregnant, your name may be listed on a pregnancy registry. This is to track the outcome of the pregnancy and to evaluate any effects of ethosuximide on the baby. Ethosuximide passes into breast milk and could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby. Ethosuximide should not be given to a child younger than 3 years old.

How should I take Zarontin (ethosuximide)?


Take exactly as prescribed by your doctor. Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label.


Your doctor may occasionally change your dose to make sure you get the best results.


Ethosuximide can lower blood cells that help your body fight infections. This can make it easier for you to bleed from an injury or get sick from being around others who are ill. Your blood may need to be tested often. Your kidney and liver function may also need to be tested. Visit your doctor regularly.


Call your doctor at once if you have any unusual bleeding, weakness, or any signs of infection, including flu-like symptoms. These symptoms may first develop even after you have been using the medication for several months. Do not stop using ethosuximide without first talking to your doctor, even if you feel fine. You may have increased seizures if you stop using ethosuximide suddenly. You may need to use less and less before you stop the medication completely.

Contact your doctor if your seizures get worse or you have them more often while taking ethosuximide.


Wear a medical alert tag or carry an ID card stating that you take ethosuximide. Any medical care provider who treats you should know that you take seizure medication.

Use ethosuximide regularly to get the most benefit. Get your prescription refilled before you run out of medicine completely.


Store at room temperature away from moisture and heat.

What happens if I miss a dose?


Take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. 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 nausea, vomiting, extreme drowsiness, and weak or shallow breathing.


What should I avoid while taking Zarontin (ethosuximide)?


Do not drink alcohol. It can increase certain side effects of ethosuximide. This medication may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.

Avoid being near people who are sick or have infections. Tell your doctor at once if you develop signs of infection.


Zarontin (ethosuximide) side effects


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

Report any new or worsening symptoms to your doctor, such as: mood or behavior changes, anxiety, depression, panic attacks, trouble sleeping, or if you feel impulsive, irritable, agitated, hostile, aggressive, restless, hyperactive (mentally or physically), or have thoughts about suicide or hurting yourself.


Call your doctor at once if you have a serious side effect such as:

  • fever, chills, flu symptoms, sore throat, swollen glands, feeling very weak;




  • easy bruising, unusual bleeding (nose, mouth, vagina, or rectum), purple or red pinpoint spots under your skin;




  • joint pain or swelling with mild fever, muscle aches, chest pain when breathing;




  • patchy skin color, red spots, or a butterfly shaped skin rash over your cheeks and nose (worsens in sunlight);




  • skin rash, severe tingling, numbness, pain, muscle weakness;




  • confusion, hallucinations, unusual thoughts or behavior, extreme fear;




  • 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; or




  • worsening of seizures.



Less serious side effects may include:



  • upset stomach, mild nausea, stomach cramps, diarrhea, weight loss;




  • swelling in your tongue or gums;




  • headache, dizziness, drowsiness, feeling tired;




  • lack of balance or coordination; or




  • unusual vaginal bleeding.



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 Zarontin (ethosuximide)?


Cold or allergy medicine, sedatives, narcotic pain medicine, sleeping pills, muscle relaxers, and medicine for depression or anxiety can add to sleepiness caused by ethosuximide. Tell your doctor if you regularly use any of these medicines, or any other seizure medication.

Before taking ethosuximide, tell your doctor about all other seizure medications you use, especially:



  • phenobarbital (Solfoton);




  • phenytoin (Dilantin); or




  • valproic acid (Depakene, Stavzor).



This list is not complete and other drugs may interact with ethosuximide. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.



More Zarontin resources


  • Zarontin Side Effects (in more detail)
  • Zarontin Use in Pregnancy & Breastfeeding
  • Drug Images
  • Zarontin Drug Interactions
  • Zarontin Support Group
  • 4 Reviews for Zarontin - Add your own review/rating


  • Zarontin Prescribing Information (FDA)

  • Zarontin MedFacts Consumer Leaflet (Wolters Kluwer)

  • Zarontin Monograph (AHFS DI)

  • Zarontin Advanced Consumer (Micromedex) - Includes Dosage Information

  • Ethosuximide Prescribing Information (FDA)

  • Ethosuximide Professional Patient Advice (Wolters Kluwer)



Compare Zarontin with other medications


  • Seizures


Where can I get more information?


  • Your pharmacist can provide more information about ethosuximide.

See also: Zarontin side effects (in more detail)