Reyvow ® (lasmiditan) tablets CV

50 mg, 100 mg

This information is provided in response to your request. Resources may contain information about doses, uses, formulations and populations different from product labeling. See Prescribing Information above, if applicable.

REYVOW® (lasmiditan): Absorption and Distribution

Reyvow (lasmiditan) is rapidly absorbed after oral administration. In patients with migraine, absorption or pharmacokinetics of lasmiditan was similar during a migraine attack or during the interictal period.

Additional Information Regarding Absorption and Distribution

Following oral administration, lasmiditan is rapidly absorbed with a median Tmax of 1.8 hours.1

In patients with migraine, the absorption or PK of lasmiditan was not different during a migraine attack versus during the interictal period.1

The oral bioavailability over the clinical dose range of 50 mg to 200 mg is predicted to be 50% to 58%, based on the results from a population PK analysis.2

Lasmiditan may be taken with or without food as administration with meals was not associated with a clinically relevant effect on exposure to lasmiditan.1

Coadministration of lasmiditan with a high-fat meal

  • increased mean lasmiditan Cmax and AUC values by 22% and 19%, respectively, and

  • delayed the median Tmax by 1 hour.1

The human plasma protein binding of lasmiditan is

  • approximately 55% to 60%, and

  • independent of concentration between 15 and 500 ng/mL.1

Enclosed Prescribing Information

REYVOW® (lasmiditan) tablets, for oral use, CV, Lilly

References

1. Reyvow [package insert]. Indianapolis, IN: Eli Lilly and Company; 2020.

2. Data on file, Eli Lilly and Company and/or one of its subsidiaries.

Glossary

AUC = area under the concentration

Cmax = maximum observed drug concentration

PK = pharmacokinetics

Tmax = time of maximum observed drug concentration

Date of Last Review: November 08, 2018

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