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)

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 Category	Explanation
All Trimesters	C	Animal 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

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)

Dronal

Dronal may be available in the countries listed below.

Ingredient matches for Dronal

Alendronic Acid

Alendronic Acid sodium trihydrate (a derivative of Alendronic Acid) is reported as an ingredient of Dronal in the following countries:

• Italy

International Drug Name Search

Flantadin

Flantadin may be available in the countries listed below.

Ingredient matches for Flantadin

Deflazacort

Deflazacort is reported as an ingredient of Flantadin in the following countries:

• Italy


• Turkey

International Drug Name Search

Methotrexato

Methotrexato may be available in the countries listed below.

Ingredient matches for Methotrexato

Methotrexate

Methotrexate is reported as an ingredient of Methotrexato in the following countries:

• Ecuador


• Venezuela

International Drug Name Search

Naproxen Schwörer

Naproxen Schwörer may be available in the countries listed below.

Ingredient matches for Naproxen Schwörer

Naproxen

Naproxen sodium salt (a derivative of Naproxen) is reported as an ingredient of Naproxen Schwörer in the following countries:

• Germany

International Drug Name Search