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Veozah dosage · All 50 States
Veozah (fezolinetant) dosage: 45 mg once daily, liver tests before treatment, monthly for three months and at months 6 and 9, plus interactions and when to stop.
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DIRECT ANSWER
Veozah is a single fixed dose: one 45 mg tablet once daily, with or without food. There is no titration. It carries a boxed warning for liver injury, so liver blood tests are required before starting, monthly for the first three months, then at months 6 and 9. Stop and contact your clinician for symptoms such as yellowing skin, dark urine or upper-right abdominal pain.
| Strength / step | How it is used | Labeled detail | When clinicians use it | Watch for |
|---|---|---|---|---|
| 45 mg once daily | Tablet, same time daily | Only labeled dose | Moderate-to-severe menopausal hot flashes | No dose adjustment option |
| Baseline liver tests | Before first dose | Required | Everyone | Abnormal results may rule it out |
| Months 1, 2, 3, 6, 9 | Follow-up liver tests | Per current label | Everyone on treatment | Lab visits needed |
Strengths shown are from current U.S. labeling, for context only. Your clinician sets your dose based on your history.
RxNorm is the U.S. National Library of Medicine's standard naming system for medicines. These codes link each product to its official record.
No. 45 mg once daily is the only labeled dose.
Trials showed reductions in hot flash frequency within the first weeks, with effects measured at 4 and 12 weeks.
The label specifies tests through month 9, and anytime symptoms suggest liver problems.
A board-certified clinician licensed in your state reviews your intake within one business day and recommends the route that fits your history — not a template.
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WRITTEN & MEDICALLY REVIEWED BY
Kindr Health Inc. — Editorial & Clinical Team, led by Kevin Wolfe, CMO
Kindr’s clinical content is written and reviewed by board-certified clinicians who prescribe hormone therapy every day across all 50 states — menopause-focused physicians, nurse practitioners, and pharmacists working under Kindr Health, Inc.’s organizational clinical oversight. Every page is checked against current NAMS and ACOG guidance, FDA labeling, and the primary literature before publication, then re-reviewed on a rolling schedule when guidance changes.
Organizational NPI 1609792902 · Last reviewed July 3, 2026 · Editorial policy
Educational content only — not a substitute for individual medical advice, diagnosis, or treatment.
SOURCES & REFERENCES
Information on this page is for educational purposes only. Prescription medications require clinical evaluation and provider approval. Individual results vary. Not an emergency service.