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  • Prescribing Information
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  • For Consumers
    • About REYVOW
    • How REYVOW Works
    • Taking REYVOW
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    • More About Migraine
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    • About Migraine
    • Patient Profile
    • Mechanism of Action
      • Overview
      • Video
    • Pivotal Trials Efficacy
      • Clinical Trial Design
      • Pain Relief
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      • Time to Dosing
      • Most Bothersome Symptom
    • Additional Phase 3 Trial Efficacy
      • Clinical Trial Design
      • Pain Relief
      • Pain Freedom in a Single Attack
      • Pain Freedom in Multiple Attacks
      • Triptan Insufficient Responders
    • Safety Data
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      • Important Information
      • Additional Phase 3 Trial Data
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Woman walking towards door with language about offering a different option (acute treatment) for adults with migraine



A different acute treatment for migraine


REYVOW is the first and only FDA-approved ditan, a high-affinity 5-HT1F receptor agonist.1


DISCOVER THE MOA

For those situations when your adult patients experience disabling migraine pain,

Image about pain freedom


Up to 39% of patients achieved complete elimination of migraine pain at 2 hours with REYVOW1


Image showing pain freedom at 2 hours data from SPARTAN and SAMURAI clinical trials

Results of the SAMURAI and SPARTAN studies, showing the percentage of patients who achieved migraine pain freedom at 2 hours with REYVOW vs placebo.

In the SAMURAI study, 503 patients took 200 mg of REYVOW, 498 patients took 100 mg of REYVOW, and 515 patients took placebo. At 2 hours, 32% (P<.001 vs placebo) of patients achieved pain freedom when taking 200 mg, 28% (P<.001 vs placebo) of patients achieved pain freedom when taking 100 mg, and 15% of patients achieved pain freedom when taking placebo. There was a 17% difference in the percentage of patients taking 200 mg vs placebo and a 13% difference in the percentage of patients taking 100 mg vs placebo.

In the SPARTAN study, 521 patients took 200 mg of REYVOW, 523 patients took 100 mg of REYVOW, 544 patients took 50 mg of REYVOW, and 534 patients took placebo. At 2 hours, 39% (P<.001 vs placebo) of patients achieved pain freedom when taking 200 mg, 31% (P<.001 vs placebo) of patients achieved pain freedom when taking 100 mg, 28% (P=.006 vs placebo) of patients achieved pain freedom when taking 50 mg, and 21% of patients achieved pain freedom when taking placebo. There was an 18% difference in the percentage of patients taking 200 mg vs placebo, a 10% difference in the percentage of patients taking 100 mg vs placebo, and a 7% difference in patients taking 50 mg vs placebo.



View Clinical Study Design



EXPLORE EFFICACY DATA


SELECT IMPORTANT SAFETY INFORMATION

Driving Impairment
REYVOW may cause significant driving impairment. More sleepiness was reported at 8 hours following a single dose of REYVOW compared to placebo. Advise patients not to engage in potentially hazardous activities requiring complete mental alertness, such as driving a motor vehicle or operating machinery, for at least 8 hours after each dose of REYVOW. Patients who cannot follow this advice should not take REYVOW. Prescribers and patients should be aware that patients may not be able to assess their own driving competence and the degree of impairment caused by REYVOW.

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Your eligible patients can save on REYVOW

Governmental beneficiaries excluded; terms and conditions apply.

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Reference:

  1. REYVOW [Prescribing Information]. Indianapolis, IN: Lilly USA, LLC.

IMPORTANT SAFETY INFORMATION

WARNINGS AND PRECAUTIONS

Driving Impairment - REYVOW may cause significant driving impairment. In a driving study, administration of single 50 mg, 100 mg, or 200 mg doses of REYVOW significantly impaired subjects’ ability to drive. Additionally, more sleepiness was reported at 8 hours following a single dose of REYVOW compared to placebo. Advise patients not to engage in potentially hazardous activities requiring complete mental alertness, such as driving a motor vehicle or operating machinery, for at least 8 hours after each dose of REYVOW. Patients who cannot follow this advice should not take REYVOW. Prescribers and patients should be aware that patients may not be able to assess their own driving competence and the degree of impairment caused by REYVOW.

Central Nervous System Depression - REYVOW may cause central nervous system (CNS) depression, including dizziness and sedation. Because of the potential for REYVOW to cause sedation, other cognitive and/or neuropsychiatric adverse reactions, and driving impairment, REYVOW should be used with caution if used in combination with alcohol or other CNS depressants. Patients should be warned against driving and other activities requiring complete mental alertness for at least 8 hours after REYVOW is taken.

Serotonin Syndrome - In clinical trials, reactions consistent with serotonin syndrome were reported in patients treated with REYVOW who were not taking any other drugs associated with serotonin syndrome. Serotonin syndrome may also occur with REYVOW during coadministration with serotonergic drugs e.g., selective serotonin reuptake inhibitors (SSRIs), serotonin norepinephrine reuptake inhibitors (SNRIs), tricyclic antidepressants (TCAs), and monoamine oxidase (MAO) inhibitors. Serotonin syndrome symptoms may include mental status changes (e.g., agitation, hallucinations, coma), autonomic instability (e.g., tachycardia, labile blood pressure, hyperthermia), neuromuscular signs (e.g., hyperreflexia, incoordination), and/or gastrointestinal signs and symptoms (e.g., nausea, vomiting, diarrhea). The onset of symptoms usually occurs within minutes to hours of receiving a new or a greater dose of a serotonergic medication. Discontinue REYVOW if serotonin syndrome is suspected.

Medication Overuse Headache - Overuse of acute migraine drugs (e.g., ergotamines, triptans, opioids, or a combination of drugs for 10 or more days per month) may lead to exacerbation of headache (i.e., medication overuse headache). Medication overuse headache may present as migraine-like daily headaches or as a marked increase in frequency of migraine attacks. Detoxification of patients including withdrawal of the overused drugs and treatment of withdrawal symptoms (which often includes a transient worsening of headache) may be necessary.

ADVERSE REACTIONS

The most common adverse reactions associated with REYVOW (≥2% and greater than placebo in clinical studies) were dizziness, fatigue, paresthesia, sedation, nausea and/or vomiting, and muscle weakness.

ABUSE

REYVOW contains lasmiditan, a Schedule V controlled substance (C-V).
REYVOW has abuse potential. Evaluate patients for risk of drug abuse and observe them for signs of lasmiditan misuse or abuse.

See Prescribing Information and Medication Guide.
LM HCP ISI 28SEP2020

INDICATIONS

REYVOW is indicated for the acute treatment of migraine with or without aura in adults.

Limitations of Use: REYVOW is not indicated for the preventive treatment of migraine.

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