Anpheros Search · Treatment

Lasmiditan

Also known as: Rayvow · Reyvow

General information only. Anpheros does not diagnose and does not recommend treatment. Talk to a doctor or pharmacist about your situation. In an emergency, call 112 (or your local emergency number).

In short

Lasmiditan is a serotonin (5-HT) 1F receptor agonist indicated in the United States for the acute treatment of migraine with or without aura in adults. In the European Union, it is indicated for the acute treatment of the headache phase of migraine attacks, with or without aura in adults. It is not indicated for the preventive treatment of migraine.

From: Data provided by the U.S. Food and Drug Administration. · Source: European Medicines Agency (EMA), Rayvow — EPAR, 06/02/2026. © European Medicines Agency.

AI-generated summary of the sources cited on this page, checked automatically against them. Not reviewed by a clinician; not medical advice.

Codes

RxNorm
2256930 lasmiditan
EMA
EMEA/H/C/005332

Official indications

Quoted unchanged from official product information, in English. Listed alphabetically by product, not ranked.

EMA (EU) Rayvow

RAYVOW is indicated for the acute treatment of the headache phase of migraine attacks, with or without aura in adults.

Source: European Medicines Agency (EMA), Rayvow — EPAR, 06/02/2026. © European Medicines Agency.

Document date: 06/02/2026 · Official document →

FDA (USA) Reyvow

1 INDICATIONS AND USAGE REYVOW ® is indicated for the acute treatment of migraine with or without aura in adults. REYVOW ® is a serotonin (5-HT) 1F receptor agonist indicated for the acute treatment of migraine with or without aura in adults. ( 1 ) Limitations of Use REYVOW is not indicated for the preventive treatment of migraine. ( 1 ) Limitations of Use REYVOW is not indicated for the preventive treatment of migraine.

Data provided by the U.S. Food and Drug Administration.

Document date: 20260108 · Official document →

Related terms in the cited sources

Has an official indication for

In alphabetical order.

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What people report

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External resources

Questions

What is Lasmiditan approved for in the European Union?

RAYVOW is indicated for the acute treatment of the headache phase of migraine attacks, with or without aura in adults. (Source: European Medicines Agency (EMA), Rayvow — EPAR, 06/02/2026. © European Medicines Agency.)

Sources and attribution

  • Source: European Medicines Agency (EMA) — EPAR. © European Medicines Agency.
  • Data provided by the U.S. Food and Drug Administration.
  • Names other than the official source titles: Anpheros translations and plain-language names, made with AI assistance and checked automatically; the source names are in English.
  • This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.
  • Source: European Medicines Agency (EMA), Rayvow — EPAR, 06/02/2026. © European Medicines Agency.

Anpheros Search catalog 2026.10.5, published 17 October 2026. About the data →