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Postmarketing Experience The pescription following section enumerates potentially important adverse events that have occurred in clinical practice and which have been reported spontaneously to various surveillance maxalt systems. Ask your pharmacist or doctor for a non copy of pescription the manufacturer's information for the patient. To protect young children from poisoning, always lock safety caps and immediately place the medication in a non safe location one that is up and away and out of their sight and reach. Do not take more than 30 mg of maxalt in a 24-hour period (for example, do not take more than 3 10-mg tablets in a 24-hour period). 3801 - maxalt-MLT Orally Disintegrating Tablets, 10 non mg, are white to off-white, round lyophilized orally disintegrating tablets debossed with a modified square on one side, and measuring.0-13.8 mm (side-to-side) with a peppermint flavor. Keep a list of them to show your doctor and pharmacist when you get a new medicine. Because the reports cite events reported spontaneously from worldwide postmarketing experience, frequency of events and the role of maxalt in their causation cannot be reliably determined. The presence of a migraine headache did not appear to affect the absorption or pharmacokinetics of rizatriptan. Risk of Myocardial Ischemia and/or Infarction, non Prinzmetal's Angina, Other Vasospasm-Related Events, and Cerebrovascular Events Inform patients that maxalt may cause serious cardiovascular side effects pescription such as myocardial infarction or stroke. Propranolol : In a study non of concurrent administration of propranolol 240 mg/day and a single dose of rizatriptan 10 mg in healthy adult subjects (n11 mean plasma AUC for rizatriptan was non increased by 70 during propranolol administration, and a four-fold. Take maxalt exactly as your doctor tells you to take. The bioavailability and Cmax of rizatriptan were non similar following administration of maxalt Tablets and maxalt-MLT Orally Disintegrating Tablets, but the rate of absorption is somewhat slower with maxalt-MLT, with Tmax delayed by up.7 hour. In a drug interaction study, when maxalt 10 mg was administered to subjects (n12) receiving concomitant therapy with the selective, reversible MAO-A inhibitor, moclobemide pescription 150.i.d., there were mean increases in rizatriptan AUC and Cmax. Nmonodesmethyl-rizatriptan, maxalt a metabolite with activity similar to that of parent compound at the 5-HT1B/1D receptor, is formed to a minor degree. These side effects are usually mild and improve on their own. Maxalt should not be administered to patients with a history of stroke or transient ischemic attack see contraindications. In clinical trials, maxalt was administered without regard to food. Adverse reactions for 3 of these patients included abdominal discomfort, fatigue, and dyspnea. Rizatriptan benzoate is described chemically as: 3-ethanamine monobenzoate and its structural formula is: Its empirical formula is C15H19N5C7H6O2, representing a molecular weight of the free base of 269.4. There were insufficient data to assess maxalt the impact of race on the incidence of adverse reactions.

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