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Frequently reported treatment-emergent adverse events (a) by percentage of patients and (b) by percentage of attacks (safety population).
AE: adverse event; MedDRA: Medical Dictionary for Regulatory Activities.
Note: Reported by ≥ 2% of patients in either treatment group. An AE that started or worsened within 48 hours after the last dose (either the first or the second dose) of lasmiditan was considered treatment-emergent. AEs were coded using MedDRA Version 21.0.
