Indications |
Oral Acute migraine attacks Adult: Initially, 10 mg. If ineffective, 2nd dose should not be taken for the same attack. If symptoms recur after initial response, a further dose of 10 mg may be given. Doses should be separated by at least 2 hr. Max: 20 mg/24 hr. If patient is also taking propanolol, initiate with 5 mg. Max: 10 mg/24 hr. Ensure that the 2 drugs are separated by at least 2 hr. Renal impairment: For mild-moderate impairment, initate with 5 mg. Further dose of 5 mg may be taken after an interval of at least 2 hr. Max: 10 mg/24 hr. Avoid in severe impairment. Hepatic impairment: For mild-moderate impairment, initate with 5 mg. Further dose of 5 mg may be taken after an interval of at least 2 hr. Max: 10 mg/24 hr. Avoid in severe impairment. Special Populations: In patients with mild to moderate hepatic or renal impairment: Dose reduction to 5 mg. For recurrence of headache: Further dose of 5 mg after 2-hr interval. Max dose: 10 mg/day. In patients receiving propranolol: Similar dose reduction; 2 drugs should be separated for at least 2 hrs. |
Contraindications |
History of MI, peripheral vascular disease, transient ishaemic attack, ischaemic heart disease or Prinzmetal's angina; uncontrolled hypertension; basilar or hemiplegic migraine; severe hepatic or renal impairment. Adolescent <18 yr. |
Warnings / Precautions |
Elderly; mild to moderate hepatic or renal impairment; coronary artery disease; pregnancy, lactation. May cause drowsiness. History of seizures. Ensure an interval of at least 24 hr after stopping an ergotamine compound and starting a serotonin (5-HT1) agonist. |
Adverse Reactions |
Increased BP, chest pain, palpitation; skin flushing; dyspnoea; nausea, abdominal pain, dry mouth; dizziness, drowsiness, fatigue. Potentially Fatal: Toxic epidermal necrolysis. |
Overdose Reactions |
May cause hypertension and CV symptoms. Gastric lavage using activated charcoal may be considered. Monitor ECG and clinical status of the patient. |
Drug Interactions |
Increased serum concentrations with propranolol. Increased risk of vasospastic reactions when used with ergotamine and methysergide. Concurrent use with SSRIs may increase risk of serotonin syndrome. Potentially Fatal: Concurrent use with or within 2 wk of stopping MAOI treatment. See Below for More rizatriptan Drug Interactions |
Food Interactions |
Absorption delayed. Concurrent use with St John's wort may increase risk of adverse reactions. |
Mechanism of Actions |
Rizatriptan is a selective serotonin (5-HT1) agonist in cranial arteries responsible for vasoconstriction and reduction of inflammation associated with antidromic neuronal transmission. Absorption: Bioavailability: about 40-45%. Distribution: Protein binding: 14%. Metabolism: Primarily by monoamine oxidase type A. Excretion: About 14% of an oral dose is excreted unchanged in the urine. Plasma half-life: about 2-3 hr. |
Administration |
Tab: May be taken with or without food. Orally disintegrating tab: May be taken with or without food. (Place on the tongue & allow to dissolve; it can then be swallowed w/ the saliva.) |
Storage Conditions |
Oral: Store at 15-30°C. |
ATC Classification |
N02CC04 - rizatriptan ; Belongs to the class of selective serotonin (5HT1) agonists preparations. Used to relieve migraine. |
Storage |
Oral: Store at 15-30°C. |
Available As |
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Rizatriptan
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Rizatriptan Containing Brands
Rizatriptan is used in following diseases
Drug - Drug Interactions of Rizatriptan
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