UPDATE 1-Eli Lilly's migraine treatment wins U.S. FDA approval [Reuters]
Eli Lilly and Company (LLY)
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Source: Reuters
Eli Lilly's migraine treatment wins U.S. FDA approval (Reuters) - The U.S. Food and Drug Administration said on Friday it had approved Eli Lilly and Co’s migraine drug, Reyvow. The drug has been approved to treat acute migraine with or without aura, a sensory phenomenon or visual disturbance, in adults. Lilly acquired Reyvow, formerly called lasmiditan, in a deal here Lilly said the price of Reyvow will be determined closer to the time of commercial availability. According to the Migraine Research Foundation, roughly 39 million Americans suffer from migraine headaches. The FDA advises patients not to drive or operate machinery for at least eight hours after taking Reyvow, as the drug causes dizziness and sedation. Reporting by Shivani Singh; Editing by Shinjini Ganguli Our Standards: The Thomson Reuters Trust Principles.
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