Maxalt and Maxalt-MLT |
rizatriptan benzoate |
Article: Rizatriptan
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| Rizatriptan | |
| Systematic (IUPAC) name | |
| N,N-dimethyl-2- [5-(1,2,4-triazol-1-ylmethyl)- 1H-indol-3-yl]ethanamine | |
| Identifiers | |
| CAS number | 145202-66-0 |
| ATC code | N02CC04 |
| PubChem | 5078 |
| DrugBank | APRD00008 |
| Chemical data | |
| Formula | C15H19N5 |
| Mol. weight | 269.345 g/mol |
| Pharmacokinetic data | |
| Bioavailability | 45% |
| Protein binding | 14% |
| Metabolism | MAO |
| Half life | 2-3 hours |
| Excretion | 82% urine; 12% feces |
| Therapeutic considerations | |
| Pregnancy cat. | C |
| Legal status | |
| Routes | tablet |
| Indicated for:
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| Contraindications:
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| Side effects: Severe:
Atypical sensations:
Cardiovascular:
Ear, nose, and throat:
Gastrointestinal:
Muscular:
Neurological:
Respiratory:
Skin:
Miscellaneous:
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Rizatriptan (Maxalt®) is a triptan drug developed by Merck & Co. for the treatment of migraine headaches. It is available in strengths of 5 and 10 mg as tablets and orally disintegrating tablets (Maxalt-MLT).
Maxalt obtained approval by the Food and Drug Administration (FDA) on June 29, 1998. It represents a second-generation triptan.
Rizatriptan is available only by prescription in the United States and Canada.
This medication is used to treat acute migraine attacks. This drug does not prevent future migraine attacks.

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