Brand Name

Reyvow

Generic Name
Lasmiditan
View Brand Information
FDA approval date: October 11, 2019
Form: Tablet

What is Reyvow (Lasmiditan)?

For people who live with migraines, even a normal day can be derailed by sudden, intense pain, sensitivity to light and sound, and overwhelming fatigue. Finding a medication that brings real, fast relief can make all the difference. Reyvow (lasmiditan) is a prescription medication developed specifically to treat acute migraine attacks, helping patients regain control when migraines strike. 

Reyvow belongs to a newer class of migraine medications known as serotonin (5-HT₁F) receptor agonists, also called ditans. Unlike older migraine drugs such as triptans, which constrict blood vessels, Reyvow works without affecting blood flow making it an important option for patients who cannot take triptans due to cardiovascular concerns. Approved by the U.S. Food and Drug Administration (FDA) in 2019, Reyvow represents a modern, targeted approach to migraine management, offering relief when symptoms begin. 

What does Reyvow do? 

Reyvow is used for the acute treatment of migraine attacks with or without aura in adults. It is not meant for the prevention of migraines but rather to relieve symptoms once an attack begins. 

When taken at the onset of a migraine, Reyvow can help reduce or eliminate pain, nausea, and sensitivity to light and sound. Many patients report being able to return to daily activities within a few hours after taking the medication. 

Clinical studies show that Reyvow provides meaningful relief: in trials, up to 40% of patients were pain-free within two hours of taking a dose, and many also reported being free from their most bothersome migraine symptoms, such as nausea or light sensitivity (FDA, 2024). 

Because Reyvow works through a different mechanism than triptans, it can be a valuable alternative for people who experience side effects or have health conditions that prevent them from using triptan medications. 

How does Reyvow work? 

Reyvow’s active ingredient, lasmiditan, targets serotonin 5-HT₁F receptors in the brain. These receptors play a key role in controlling pain pathways and inflammation involved in migraine attacks. 

During a migraine, the trigeminal nerve, a major pain pathway in the head becomes activated, leading to the release of inflammatory chemicals and transmission of pain signals to the brain. Lasmiditan binds to 5-HT₁F receptors on these nerve endings, helping block the release of pain-causing neurotransmitters and calm nerve activity. 

This action helps stop a migraine attack without constricting blood vessels, unlike triptans that target 5-HT₁B and 5-HT₁D receptors. Clinically, this makes Reyvow a safer option for individuals with heart disease, high blood pressure, or a history of stroke, who may not be able to take vasoconstrictive migraine drugs. 

The medication’s non-vascular mechanism is a major advancement in migraine care focusing directly on pain signaling rather than blood vessel changes. 

Reyvow side effects 

Reyvow is generally well-tolerated, but like all medications, it can cause side effects. Most are mild and tend to resolve as the body adjusts to the medication. 

Common side effects may include: 

  • Dizziness or fatigue 
     
  • Tingling sensations (paresthesia) 
     
  • Drowsiness or sedation 
     
  • Nausea 
     
  • Dry mouth 

Because Reyvow can cause significant drowsiness, patients are advised not to drive or operate machinery for at least 8 hours after taking it,  even if they feel fully awake. This safety precaution is required by the FDA because the medication may impair coordination and alertness longer than patients expect. 

Serious side effects (rare) may include: 

  • Allergic reactions such as rash, itching, or swelling of the face or throat 
     
  • Serotonin syndrome, especially if taken with other serotonergic drugs like certain antidepressants (symptoms include agitation, confusion, sweating, or muscle stiffness) 

People with liver disease, kidney disease, or a history of substance use disorder should discuss these conditions with their doctor before starting Reyvow. It should also be used cautiously in patients taking medications that affect serotonin levels. 

If any severe or unexpected reactions occur, medical attention should be sought immediately. 

Reyvow dosage 

Reyvow, an oral tablet, treats acute migraine attacks, not as a daily preventive. Take a single dose at migraine onset; do not exceed one dose in 24 hours or combine with other migraine-specific medications without medical advice. Dosage is individualized by a healthcare provider. 

Doctors monitor patients for side effects like dizziness, fatigue, or coordination changes. Due to Reyvow’s sedative effects, providers assess a patient’s routine and other medications for safe use. Older adults or those with liver/kidney issues may need dose adjustments or closer observation. Consistent communication with the provider ensures safety and effectiveness. 

Does Reyvow have a generic version? 

As of 2025, Reyvow (lasmiditan) does not have a generic version available in the United States. It is sold exclusively under the brand name Reyvow, manufactured by Eli Lilly and Company. However, international versions may exist in other markets. 

As a new, patented drug, a generic version is years away. Patients can inquire about savings programs or insurance coverage. Once available, generic versions must meet FDA quality, safety, and effectiveness standards. 

Conclusion 

Reyvow (lasmiditan) is an innovative treatment designed to stop migraines quickly and effectively especially for patients who cannot use traditional migraine medications. By targeting the brain’s pain pathways without constricting blood vessels, it provides a much-needed alternative for those with cardiovascular risks or poor response to triptans. 

While causing drowsiness, Reyvow is a safe and effective migraine treatment when used responsibly and with medical supervision. It can significantly reduce migraine pain and improve quality of life. Open communication with a healthcare provider is vital to monitor effects and side effects, ensuring Reyvow is a trusted part of a personalized migraine management plan. 

References 

  1. U.S. Food and Drug Administration (FDA). (2024). Reyvow (lasmiditan) prescribing information. Retrieved from https://www.accessdata.fda.gov 
     
  1. Mayo Clinic. (2024). Lasmiditan (oral route) description and precautions. Retrieved from https://www.mayoclinic.org 
     
  1. MedlinePlus. (2024). Lasmiditan: Drug information. National Library of Medicine. Retrieved from https://medlineplus.gov 
     
  1. National Institutes of Health (NIH). (2024). Migraine treatment advances: Ditans and gepants. Retrieved from https://www.nih.gov 
     

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Related Clinical Trials

A Phase 3, 12-Month, Open-Label Study of Lasmiditan in Pediatric Patients With Migraine - PIONEER-PEDS2

Summary: The reason for this 12-month, open-label study is to see if the study drug lasmiditan is safe and effective for the intermittent acute treatment of migraine in children aged 6 to 17. The study will last about 12 months and may include up to 7 visits.

Pediatric Options for Migraine Relief: A Randomized, Double-Blind, Placebo-Controlled Study of Lasmiditan for Acute Treatment of Migraine: PIONEER-PEDS1

Summary: The reason for this study is to see if lasmiditan is safe and effective in children aged 6 to 17 with migraine. The study will last up to 20 weeks and may include up to 4 visits.

Italian Real-life Multicenter Observational Study on Efficacy, Tolerability, and Safety of Innovative Drugs (Monoclonal Antibodies, Gepants, Ditans, Sumatriptan-naproxen) for Preventive or Acute Migraine Treatment.

Summary: Approved by the Food and Drug Administration (FDA) and the European Medicine Agency (EMA) starting in 2018, anti-CGRP monoclonal antibodies (anti-CGRP mAbs) represent the first true revolution in the preventive treatment of migraine due to their selectivity and specificity. To date, four anti-CGRP mAbs have been developed for the preventive treatment of migraine: eptinezumab, erenumab, fremanezuma...

Brand Information

Reyvow (lasmiditan)
1INDICATIONS AND USAGE
REYVOW
2DOSAGE AND ADMINISTRATION
The recommended dose of REYVOW is 50 mg, 100 mg, or 200 mg taken orally, as needed. No more than one dose should be taken in 24 hours, and REYVOW should not be taken unless the patient can wait at least 8 hours between dosing and driving or operating machinery
A second dose of REYVOW has not been shown to be effective for the same migraine attack.
The safety of treating an average of more than 4 migraine attacks in a 30-day period has not been established.
REYVOW may be taken with or without food.
Administer tablets whole; do not split, crush, or chew.
3DOSAGE FORMS AND STRENGTHS
REYVOW (lasmiditan) tablets are available in two strengths:
  • 50 mg tablet: light gray, oval, film coated, tablets with “L-50” debossed on one side and “4312” on the other
  • 100 mg tablet: light purple, oval, film coated, tablets with “L-100” debossed on one side and “4491” on the other
4CONTRAINDICATIONS
None.
5ADVERSE REACTIONS
The following clinically significant adverse reactions are described elsewhere in the labeling:
  • Driving Impairment
  • Central Nervous System Depression
  • Serotonin Syndrome
  • Medication Overuse Headache
5.1Clinical Trials Experience
Because clinical studies are conducted under widely varying conditions, adverse reaction rates observed in the clinical studies of a drug cannot be directly compared to rates in the clinical studies of another drug and may not reflect the rates observed in practice.
The safety of REYVOW has been evaluated in 4,878 subjects who received at least one dose of REYVOW. In 2 placebo-controlled, Phase 3 trials in adult patients with migraine (Studies 1 and 2), a total of 3,177 patients received REYVOW 50, 100, or 200 mg
Long-term safety was assessed for 2,030 patients, dosing intermittently for up to 12 months in a long-term safety study. Of these, 728 patients were exposed to 100 mg or 200 mg for at least 3 months, 361 patients were exposed to these doses for at least 6 months, and 180 patients were exposed to these doses for at least 12 months, all of whom treated at least 2 migraine attacks per month on average. In that study, 14% (148 out of 1,039) in the 200 mg dose group, and 11% (112 out of 991) in the 100 mg dose group withdrew from the trial because of an adverse event. The most common adverse event resulting in discontinuation in the long-term safety study (greater than 2%) was dizziness.
Table 1 shows adverse reactions that occurred in at least 2% of patients treated with REYVOW and more frequently than in patients who received placebo in Studies 1 and 2. The most common adverse reactions (at least 5%) were dizziness, fatigue, paresthesia, and sedation.
6DESCRIPTION
REYVOW (lasmiditan) is a serotonin (5-HT) 1F receptor agonist for oral administration. The chemical name of lasmiditan hemisuccinate is 2,4,6-trifluoro-N-[6-(1-methylpiperidine-4-carbonyl)pyridine-2-yl]benzamide hemisuccinate. It has the empirical formula of C
Structural Formula
Lasmiditan hemisuccinate is a white, crystalline powder that is sparingly soluble in water, slightly soluble in ethanol, and soluble in methanol. A 1 mg/mL aqueous solution of lasmiditan hemisuccinate has a pH of 6.8 at ambient conditions.
REYVOW 50 mg tablets contain 50 mg lasmiditan (equivalent to 57.824 mg lasmiditan hemisuccinate) and the inactive ingredients as follows:
Excipients – croscarmellose sodium, magnesium stearate, microcrystalline cellulose, pregelatinized starch, sodium lauryl sulfate.
Color mixture ingredients – black ferric oxide, polyethylene glycol, polyvinyl alcohol, talc, titanium dioxide.
REYVOW 100 mg tablets contain 100 mg lasmiditan (equivalent to 115.65 mg lasmiditan hemisuccinate) and the inactive ingredients as follows:
Excipients – croscarmellose sodium, magnesium stearate, microcrystalline cellulose, pregelatinized starch, sodium lauryl sulfate.
Color mixture ingredients – black ferric oxide, polyethylene glycol, polyvinyl alcohol, red ferric oxide, talc, titanium dioxide.
7PATIENT COUNSELING INFORMATION
Advise the patient to read the FDA-approved patient labeling (
Driving Impairment – 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 taking each dose of REYVOW. Patients who cannot follow this advice should not take REYVOW. Patients may not be able to assess their own driving competence and the degree of impairment caused by REYVOW [see Warnings and Precautions (.
CNS Depression – Inform patients that REYVOW may cause dizziness and sedation. Advise patients to use caution if taking REYVOW in combination with alcohol or other CNS depressants [see Warnings and Precautions (.
Serotonin Syndrome – Caution patients about the risk of serotonin syndrome with the use of REYVOW, particularly during combined use with serotonergic medications such as SSRIs, SNRIs, TCAs, or MAO inhibitors [see Warnings and Precautions (.
Medication Overuse Headache – Inform patients that use of drugs to treat migraine attacks for 10 or more days per month may lead to an exacerbation of headache, and encourage patients to record headache frequency and drug use (e.g., by keeping a headache diary) [see Warnings and Precautions (.
Hypersensitivity – Advise patients to seek immediate medical attention if they experience any symptoms of serious or severe hypersensitivity reaction [see Adverse Reactions (.
Abuse and Dependence – Advise patients that REYVOW is a federally controlled substance because it has the potential to be abused [see Drug Abuse and Dependence (. Advise patients to keep their medication secure.
Pregnancy
  • Advise patients to notify their healthcare provider if they become pregnant during treatment or plan to become pregnant
  • Advise patients that there is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to REYVOW during pregnancy
Nursing Mothers – Inform patients to notify their healthcare provider if they are breastfeeding or plan to breastfeed [see Use in Specific Populations (.
Administration – Advise patients to swallow tablets whole (do not split, crush, or chew) [see Dosage and Administration (.
Literature revised September 2022
Marketed by: Lilly USA, LLC, Indianapolis, IN 46285, USACopyright © 2019, 2022, Eli Lilly and Company. All rights reserved.
REY-0007-USPI-20220915