Budesonide Meda

Budesonide Meda may be available in the countries listed below.

Ingredient matches for Budesonide Meda

Budesonide

Budesonide is reported as an ingredient of Budesonide Meda in the following countries:

• Netherlands

International Drug Name Search

Lomidine

Lomidine may be available in the countries listed below.

Ingredient matches for Lomidine

Loratadine

Loratadine is reported as an ingredient of Lomidine in the following countries:

• Taiwan

International Drug Name Search

Clavoral

Clavoral may be available in the countries listed below.

In some countries, this medicine may only be approved for veterinary use.

Ingredient matches for Clavoral

Amoxicillin

Amoxicillin trihydrate (a derivative of Amoxicillin) is reported as an ingredient of Clavoral in the following countries:

• Netherlands

Clavulanate

Clavulanic Acid is reported as an ingredient of Clavoral in the following countries:

• Netherlands

International Drug Name Search

Rythmol

Pronunciation: proe-PA-fen-one
Generic Name: Propafenone
Brand Name: Rythmol

Rythmol has not been shown to improve the rate of survival in patients with an abnormal heart rhythm. For this reason, Rythmol should only be used for certain life-threatening abnormal heart rhythms. Talk with your doctor about the risks and benefits of using Rythmol.

Rythmol is used for:

Treating certain types of life-threatening irregular heartbeat (ventricular arrhythmias). It is also used to help maintain a normal heart rhythm in certain patients who have certain types of irregular heartbeat (paroxysmal atrial fibrillation/flutter [PAF], paroxysmal supraventricular tachycardia [PSVT]).

Rythmol is a class 1C antiarrhythmic medicine. It works in the heart to stabilize its action and regulate heartbeat.

Do NOT use Rythmol if:

• you are allergic to any ingredient in Rythmol


• you have uncontrolled congestive heart failure, shock caused by severe heart problems, slow heartbeat, very low blood pressure, abnormal blood electrolyte levels, or certain breathing problems (eg, chronic bronchitis or emphysema)


• you have certain types of irregular heartbeat (eg, sick sinus syndrome, heart block) and you do not have a permanent pacemaker


• you are taking another antiarrhythmic (eg, amiodarone, quinidine), cisapride, an HIV protease inhibitor (eg, ritonavir), halofantrine, a ketolide (eg, telithromycin), a macrolide antibiotic (eg, erythromycin), nilotinib, pimozide, a quinolone antibiotic (eg, ciprofloxacin), tetrabenazine, toremifene, vandetanib, or ziprasidone

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

Before using Rythmol:

Some medical conditions may interact with Rythmol. 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


• if you have kidney or liver problems, lung or breathing problems, lupus, or myasthenia gravis (muscle weakness)


• if you have a certain abnormal blood test (antinuclear antibody [ANA] test)


• if you use an artificial pacemaker or if you smoke tobacco


• if you have low blood pressure or a history of an irregular heartbeat (eg, widening of the QRS complex, atrioventricular [AV] block, ventricular tachycardia or fibrillation), a heart attack, or other heart problems (eg, coronary artery disease, heart failure)

Some MEDICINES MAY INTERACT with Rythmol. Tell your health care provider if you are taking any other medicines, especially any of the following:

• Antiarrhythmics (eg, amiodarone, quinidine), arsenic, astemizole, bepridil, chloroquine, cisapride, domperidone, droperidol, halofantrine, haloperidol, iloperidone, ketolides (eg, telithromycin), macrolide antibiotics (eg, erythromycin), maprotiline, methadone, nilotinib, pentamidine, phenothiazines (eg, thioridazine), pimozide, quinolone antibiotics (eg, ciprofloxacin), romidepsin, serotonin receptor antagonist antiemetics (eg, dolasetron), tacrolimus, terfenadine, tetrabenazine, toremifene, tricyclic antidepressants (eg, desipramine, imipramine), tyrosine kinase receptor inhibitors (eg, dasatinib), vandetanib, or ziprasidone because the risk of serious side effects, such as abnormal heart rhythms, may be increased


• Abiraterone, azole antifungals (eg, ketoconazole), cimetidine, HIV protease inhibitors (eg, ritonavir, saquinavir), selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine, paroxetine, sertraline), or serotonin-norepinephrine reuptake inhibitors (SNRIs) (eg, duloxetine, venlafaxine) because they may increase the risk of Rythmol's side effects


• Orlistat or rifamycins (eg, rifampin) because they may decrease Rythmol's effectiveness


• Anticoagulants (eg, warfarin), beta-blockers (eg, propranolol), digoxin, or lidocaine because the risk of their side effects may be increased by Rythmol

This may not be a complete list of all interactions that may occur. Ask your health care provider if Rythmol 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 Rythmol:

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

• Take Rythmol by mouth with or without food.


• Take each dose at the same time with respect to meals.


• Take Rythmol on a regular schedule to get the most benefit from it. Do not miss any doses.


• Eating grapefruit or drinking grapefruit juice may affect the amount of Rythmol in your blood. Talk with your doctor before including grapefruit or grapefruit juice in your diet.


• If you miss a dose of Rythmol, 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 Rythmol.

Important safety information:

• Rythmol may cause drowsiness or dizziness. These effects may be worse if you take it with alcohol or certain medicines. Use Rythmol with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.


• Rythmol may affect how artificial pacemakers work. Pacemakers should be monitored and programmed accordingly during therapy.


• If severe or persistent vomiting, sweating, loss of appetite or thirst, or diarrhea occurs, you will need to take care not to become dehydrated. Contact your doctor for instructions.


• Rythmol may lower the ability of your body to fight infection. Avoid contact with people who have colds or infections. Tell your doctor if you notice signs of infection, like fever, sore throat, rash, or chills.


• Tell your doctor or dentist that you take Rythmol before you receive any medical or dental care, emergency care, or surgery.


• Rythmol may decrease sperm counts in men. This could affect the ability to father a child. Discuss any questions or concerns with your doctor.


• Rythmol may interfere with certain lab tests, including ANA titers. Be sure your doctor and lab personnel know you are taking Rythmol.


• Lab tests, including electrocardiographic tests, white blood cell counts, and electrolyte levels, may be performed while you use Rythmol. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.


• Rythmol should be used with extreme caution in CHILDREN; safety and effectiveness in children have not been confirmed.


• PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of taking Rythmol while you are pregnant. Rythmol is found in breast milk. Do not breast-feed while taking Rythmol.

Possible side effects of Rythmol:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Change in taste; constipation; diarrhea; dizziness; drowsiness; dry mouth; gas; headache; light-headedness; nausea; tiredness.

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); black, tarry stools; blood in the urine; burning, numbness, or tingling; chest pain; confusion; change in the amount of urine produced or painful urination; fainting; fast or slow heartbeat; fever, chills, or sore throat; hearing problems; loss of appetite; mental or mood problems (eg, anxiety, depression); muscle weakness; new or worsened irregular heartbeat; numbness of an arm or leg; one-sided weakness; pain, swelling, or redness of the calf or legs; ringing in the ears; severe or persistent dizziness, tiredness, or weakness; severe stomach or back pain; shortness of breath; slurred speech; sudden, severe headache; sudden weight gain; swelling of the hands or feet; tremor; trouble sleeping; unusual bruising or bleeding; vomiting; vision problems (eg, blurred vision); wheezing.

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: Rythmol 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 fainting; irregular or slow heartbeat; seizures; severe dizziness or drowsiness.

Proper storage of Rythmol:

Store Rythmol at 77 degrees F (25 degrees C) in a tightly closed container. Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Rythmol out of the reach of children and away from pets.

General information:

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


• Rythmol 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.


• Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Rythmol. 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 Rythmol resources

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

• Rythmol Advanced Consumer (Micromedex) - Includes Dosage Information


• Rythmol Concise Consumer Information (Cerner Multum)


• Rythmol Monograph (AHFS DI)


• Rythmol Prescribing Information (FDA)


• Propafenone Professional Patient Advice (Wolters Kluwer)


• Propafenone Prescribing Information (FDA)


• Rythmol SR Prescribing Information (FDA)

Compare Rythmol with other medications

• Atrial Fibrillation
• Atrial Flutter
• Ventricular Tachycardia
• Wolff-Parkinson-White Syndrome

Demovarin

Demovarin may be available in the countries listed below.

Ingredient matches for Demovarin

Heparin

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

• Switzerland

International Drug Name Search

Betapace

Pronunciation: SOE-ta-lol
Generic Name: Sotalol
Brand Name: Betapace

Because Betapace may sometimes cause an abnormal or irregular heartbeat, patients who begin taking or restart Betapace should be observed in a hospital or similar setting in which heart and kidney function monitoring may be performed for at least 3 days after starting Betapace. Close monitoring of your heart or kidney function may also be needed if your dose is changed. Do not change from one brand or generic version of Betapace to another without consulting your doctor or pharmacist. Betapace is labeled specifically for ventricular arrhythmias.

Betapace is used for:

Treating certain types of irregular heartbeat (ventricular arrhythmias).

Betapace is an antiarrhythmic medicine. It works by helping the heart beat regularly for a longer period of time.

Do NOT use Betapace if:

• you are allergic to any ingredient in Betapace


• you have certain types of irregular heartbeat (eg, long QT syndrome, prolonged QT interval), shock caused by serious heart problems, uncontrolled heart failure, low blood potassium or magnesium levels, or certain lung or breathing problems (eg, asthma, chronic bronchitis, emphysema)


• you have a very slow heartbeat or certain types of irregular heartbeat (sick sinus syndrome, second- or third-degree heart block) and you do not have a permanent pacemaker


• you are taking certain antiarrhythmics (eg, amiodarone, disopyramide, dofetilide, procainamide, quinidine), bepridil, cisapride, mibefradil, nilotinib, tetrabenazine, a theophylline (eg, aminophylline), a tricyclic antidepressant (eg, amitriptyline), or vardenafil

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

Before using Betapace:

Some medical conditions may interact with Betapace. 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


• if you have breathing or lung problems (eg, chronic obstructive pulmonary disorder [COPD]); an overactive thyroid; kidney problems; diabetes; blood flow problems; a tumor on your adrenal gland; loss of appetite; increased thirst; or severe or persistent diarrhea, sweating, or vomiting


• if you have a history of other heart problems (eg, heart failure, slow or irregular heartbeat, a recent heart attack), blood electrolyte problems (eg, low blood potassium or magnesium levels), problems with the acid or base levels in your body, or episodes of low blood sugar


• if you are on dialysis or you are scheduled for surgery

Some MEDICINES MAY INTERACT with Betapace. Tell your health care provider if you are taking any other medicines, especially any of the following:

• Indomethacin because it may decrease Betapace's effectiveness


• Calcium channel blockers (eg, diltiazem, verapamil), clonidine, digoxin, diuretics (eg, furosemide, hydrochlorothiazide), guanethidine, mibefradil, or reserpine because the risk of side effects, such as low blood pressure or heart problems, may be increased


• Antiarrhythmics (eg, dronedarone, propafenone), arsenic, astemizole, bepridil, chloroquine, cisapride, dolasetron, domperidone, droperidol, fingolimod, fluconazole, halofantrine, haloperidol, iloperidone, ketanserin, macrolides and ketolides (eg, erythromycin), maprotiline, mefloquine, methadone, nilotinib, oseltamivir, paliperidone, pentamidine, phenothiazines (eg, chlorpromazine, thioridazine), pimozide, quinolones (eg, ciprofloxacin), romidepsin, saquinavir, terfenadine, tetrabenazine, tricyclic antidepressants (eg, amitriptyline), tyrosine kinase inhibitors (eg, dasatinib), vardenafil, or ziprasidone because the risk of abnormal heart rhythms may be increased


• Epinephrine, insulin, lidocaine, meglitinide antidiabetics (eg, nateglinide), or quinazolines (eg, prazosin) because the risk of their side effects may be increased by Betapace


• Beta-agonists (eg, albuterol) or theophyllines (eg, aminophylline) because their effectiveness may be decreased by Betapace

This may not be a complete list of all interactions that may occur. Ask your health care provider if Betapace 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 Betapace:

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

• Take Betapace by mouth with or without food. Try to take it the same way (either with food or without food) each time you take your dose. Check with your doctor or pharmacist if you have questions about taking Betapace with food.


• Do not take an antacid that has aluminum or magnesium in it within 2 hours before or after you take Betapace.


• Betapace works best if it is taken at the same time each day. Taking Betapace at the same time each day will also help you remember to take it.


• Continue to use Betapace even if you feel well. Do not miss any doses.


• If you miss a dose of Betapace, 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 Betapace.

Important safety information:

• Betapace may cause dizziness or lightheadedness. These effects may be worse if you take it with alcohol or certain medicines. Use Betapace with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.


• Betapace may cause dizziness, lightheadedness, or fainting; alcohol, hot weather, exercise, or fever may increase these effects. To prevent them, sit up or stand slowly, especially in the morning. Sit or lie down at the first sign of any of these effects.


• Do NOT take more than the recommended dose or change your dose without checking with your doctor.


• Tell your doctor or dentist that you take Betapace before you receive any medical or dental care, emergency care, or surgery.


• Do not suddenly stop taking Betapace. Sharp chest pain, irregular heartbeat, and, sometimes, heart attack may occur if you suddenly stop Betapace. The risk may be greater if you have certain types of heart disease. Heart disease is common and you may not know you have it. Your doctor should slowly lower your dose over several weeks if you need to stop taking it. Limit physical activity while you are lowering your dose. If new or worsened chest pain or other heart problems occur, contact your doctor right away. You may need to start taking Betapace again.


• Diabetes patients - Betapace may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.


• Diabetes patients - Betapace may hide signs of low blood sugar, such as rapid heartbeat. Be sure to watch for other signs of low blood sugar. Low blood sugar may make you anxious, sweaty, weak, dizzy, drowsy, or faint. It may also make your vision change; give you a headache, chills, or tremors; or make you more hungry. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.


• If you have a history of any severe allergic reaction, talk with your doctor. You may be at risk of an even more severe allergic reaction if you come into contact with the substance that caused your allergy. Some medicines used to treat severe allergies may also not work as well while you are taking Betapace.


• Betapace may interfere with certain lab tests. Be sure your doctor and lab personnel know you are taking Betapace.


• Lab tests, including heart and kidney function, and blood pressure monitoring, may be performed while you take Betapace. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.


• PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of taking Betapace while you are pregnant. Betapace is found in breast milk. Do not breast-feed while taking Betapace.

Possible side effects of Betapace:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Dizziness; headache; lightheadedness; mild diarrhea or nausea; tiredness; trouble sleeping.

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); abnormally fast, slow, or irregular heartbeat; changes in vision; chest pain; decreased appetite; excessive thirst; fainting; numbness of an arm or leg; severe or persistent tiredness; severe or persistent nausea, vomiting, or diarrhea; severe stomach pain; shortness of breath; sudden leg pain; sudden, severe headache, vomiting, or dizziness; unusual sweating.

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: Betapace 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 difficulty breathing; dizziness; fainting; fatigue; severe weakness; slow heartbeat.

Proper storage of Betapace:

Store Betapace at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Betapace out of the reach of children and away from pets.

General information:

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


• Betapace 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.


• Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Betapace. 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 Betapace resources

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

• Betapace Prescribing Information (FDA)


• Betapace Advanced Consumer (Micromedex) - Includes Dosage Information


• Betapace Concise Consumer Information (Cerner Multum)


• Sotalol Prescribing Information (FDA)


• Betapace AF Prescribing Information (FDA)


• Betapace AF Concise Consumer Information (Cerner Multum)


• Sorine Prescribing Information (FDA)


• Sotalol Hydrochloride Monograph (AHFS DI)

Compare Betapace with other medications

• Ventricular Arrhythmia

Lomexin

Lomexin may be available in the countries listed below.

Ingredient matches for Lomexin

Fenticonazole

Fenticonazole is reported as an ingredient of Lomexin in the following countries:

• Oman


• South Africa


• Taiwan

Fenticonazole nitrate (a derivative of Fenticonazole) is reported as an ingredient of Lomexin in the following countries:

• Austria


• Brazil


• Bulgaria


• Czech Republic


• France


• Germany


• Greece


• Italy


• Latvia


• Lithuania


• Mexico


• Portugal


• Romania


• Serbia


• Slovakia


• Spain


• Vietnam

International Drug Name Search

Apo-Nadolol

Apo-Nadolol may be available in the countries listed below.

Ingredient matches for Apo-Nadolol

Nadolol

Nadolol is reported as an ingredient of Apo-Nadolol in the following countries:

• New Zealand

International Drug Name Search

Prozamel

Prozamel may be available in the countries listed below.

Ingredient matches for Prozamel

Fluoxetine

Fluoxetine hydrochloride (a derivative of Fluoxetine) is reported as an ingredient of Prozamel in the following countries:

• Ireland

International Drug Name Search

Ziclob

Ziclob may be available in the countries listed below.

Ingredient matches for Ziclob

Cyclobenzaprine

Cyclobenzaprine hydrochloride (a derivative of Cyclobenzaprine) is reported as an ingredient of Ziclob in the following countries:

• Chile

International Drug Name Search

Rizatriptan

Pronunciation: RYE-za-TRIP-tan
Generic Name: Rizatriptan
Brand Name: Maxalt

Rizatriptan is used for:

Treating migraine headaches with or without aura (eg, flashing lights, wavy lines, dark spots) in adults. It should not be used to prevent migraines or cluster headaches.

Rizatriptan is a selective serotonin receptor agonist. It works by narrowing dilated blood vessels in the brain, relieving migraine headaches.

Do NOT use Rizatriptan if:

• you are allergic to any ingredient in Rizatriptan


• you have a history of ischemic heart disease (eg, angina, a heart attack), coronary artery disease (CAD), other moderate to severe heart problems, brain blood vessel disease (eg, a stroke, a transient ischemic attack), or other blood vessel disease (eg, Raynaud syndrome, ischemic bowel disease)


• you have uncontrolled high blood pressure


• you have certain types of migraine headache (hemiplegic, basilar)


• you are taking or have taken a monoamine oxidase inhibitor (MAOI) (eg, phenelzine) within the past 14 days


• you have used certain other migraine medicines within the past 24 hours (eg, an ergot derivative [eg, dihydroergotamine, methysergide], another serotonin 5-HT₁ receptor agonist [eg, eletriptan, rizatriptan])

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

Before using Rizatriptan:

Some medical conditions may interact with Rizatriptan. 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


• if you are very overweight, past menopause, or you smoke


• if you have a history of other types of headaches (eg, cluster headaches)


• if you have a history of diabetes, kidney or liver problems, heart problems, chest pain, shortness of breath, high blood cholesterol, high blood pressure


• if a family member has had heart disease or a stroke


• if you are a man who is over 40 years old


• if you are on dialysis

Some MEDICINES MAY INTERACT with Rizatriptan. Tell your health care provider if you are taking any other medicines, especially any of the following:

• MAOIs (eg, phenelzine), selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine), serotonin-norepinephrine reuptake inhibitors (SNRIs) (eg, venlafaxine), or sibutramine because severe side effects, such as a reaction that may include fever, blood pressure changes, mental changes, confusion, irritability, agitation, delirium, and coma, may occur


• Beta-blockers (eg, propranolol) or ergot alkaloids (eg, ergotamine) because they may increase the risk of Rizatriptan's side effects

This may not be a complete list of all interactions that may occur. Ask your health care provider if Rizatriptan 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 Rizatriptan:

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

• An extra patient leaflet is available with Rizatriptan. Talk to your pharmacist if you have questions about this information.


• Take Rizatriptan by mouth with or without food.


• Take Rizatriptan with plenty of fluid.


• It is best to take a dose of Rizatriptan as soon as you notice symptoms of a migraine attack.


• If your migraine symptoms go away and then come back, you may take a second dose as directed by your doctor. Wait at least 2 hours between doses.


• If your symptoms do not improve after the first dose, do not take a second dose for the same attack. Contact your doctor.


• Do not take more than the amount prescribed by your doctor in a 24-hour period or treat more than 4 headaches within 30 days without checking with your doctor.


• If you miss a dose of Rizatriptan and you still have a headache, follow your doctor's dosing instructions. Contact your doctor right away if you are unsure of what to do if you miss a dose. Do not take Rizatriptan more often than prescribed. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Rizatriptan.

Important safety information:

• Rizatriptan may cause dizziness or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Rizatriptan with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it.


• Rizatriptan is not intended to prevent or reduce the number of migraine attacks that you experience.


• If you have a headache that is different from your usual migraine attacks, check with your doctor before using Rizatriptan.


• Rarely, serious heart problems (eg, a heart attack, irregular heartbeat) have been reported within a few hours of using Rizatriptan. Contact your doctor at once if fast or irregular heartbeat; chest, jaw, or neck pain or numbness; numbness of an arm or leg; severe stomach pain, dizziness, or vomiting; fainting; or vision changes occur. Discuss any questions or concerns with your doctor.


• Serotonin syndrome is a possibly fatal syndrome that can be caused by Rizatriptan. Your risk may be greater if you take Rizatriptan with certain other medicines (eg, MAOIs, SNRIs, SSRIs). Symptoms may include agitation; confusion; hallucinations; coma; fever; fast or irregular heartbeat; tremor; muscle spasms; trouble walking; excessive sweating; and nausea, vomiting, or diarrhea. Contact your doctor at once if you have any of these symptoms.


• Lab tests, including heart function, may be performed while you use Rizatriptan. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.


• Rizatriptan should not be used in CHILDREN younger than 18 years old; safety and effectiveness in these children have not been confirmed.


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

Possible side effects of Rizatriptan:

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Diarrhea; dizziness; drowsiness; fatigue; nausea; weakness.

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); bloody diarrhea; burning, numbness, or tingling of the hands or feet; chest heaviness; chest, neck, or jaw pain, tightness, or pressure; confusion; decreased coordination; excessive sweating; fainting; fast, slow, or irregular heartbeat; fever; hallucinations; mental or mood changes (eg, agitation); muscle spasms; numbness of an arm or leg; one-sided weakness; seizure; severe nausea, vomiting, or diarrhea; severe or persistent headache or dizziness; shortness of breath; slurred speech; stomach pain; tremor; unusual weakness; very cold or blue fingers or toes; vision changes or loss of vision.

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: Rizatriptan 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 (http://www.aapcc.org ), or emergency room immediately. Symptoms may include fainting; slow, fast, or irregular heartbeat; unusual dizziness or drowsiness; vomiting.

Proper storage of Rizatriptan:

Store Rizatriptan at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Store away from heat, moisture, and light. Keep Rizatriptan out of the reach of children and away from pets.

General information:

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


• Rizatriptan 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.


• Check with your pharmacist about how to dispose of unused medicine.

This information is a summary only. It does not contain all information about Rizatriptan. 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 Rizatriptan resources

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

• rizatriptan Advanced Consumer (Micromedex) - Includes Dosage Information


• Maxalt Prescribing Information (FDA)


• Maxalt Monograph (AHFS DI)


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