Yes, lasmiditan, marketed under the brand name Reyvow, is FDA approved. The FDA granted approval for lasmiditan on October 11, 2019. This approval marked the introduction of lasmiditan as a novel treatment option for the acute management of migraine attacks in adults, with or without aura.
Lasmiditan belongs to a class of drugs known as ditans and is used as an abortive medication for migraine attacks, meaning it treats migraines that have already started rather than preventing them. Unlike triptans, which are the standard treatment for migraines and work by constricting blood vessels, lasmiditan does not cause vasoconstriction, making it a suitable option for patients who might have cardiovascular risks.
Lasmiditan functions as a serotonin (5-HT)1F receptor agonist. Although the exact mechanism of action is not completely understood, it is believed to work by blocking pain pathways in the brain. This action helps alleviate the symptoms of a migraine attack.
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Potential Side Effects: Common side effects of lasmiditan include dizziness, sleepiness, numbness, tiredness, and tingling. More serious side effects can include serotonin syndrome, characterized by mental changes, fast heartbeat, changes in blood pressure, high body temperature, tight muscles, and nausea.
Drug Interactions: Lasmiditan can interact with other medications, particularly those that lower heart rate, increase blood pressure, or cause drowsiness. It can also interact with antidepressants like SSRIs, SNRIs, TCAs, and MAOIs. Always inform your healthcare provider about all the medications you are taking to avoid potential interactions.
Lasmiditan (Reyvow) was FDA approved on October 11, 2019, providing a new option for the acute treatment of migraine attacks in adults. It offers an alternative to triptans, especially for patients who cannot take medications that cause vasoconstriction. As with any medication, it is essential to follow your healthcare provider’s instructions and be aware of potential side effects and interactions.
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