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FDA Updates Veozah Label with Warning for Rare but Serious Liver Injury

• The FDA has issued a warning for Veozah (fezolinetant) regarding rare but serious liver injury in patients using the drug for hot flashes due to menopause. • The updated label includes recommendations for increased frequency of liver blood testing during treatment, specifically monthly for the first two months. • Patients are advised to immediately stop Veozah and contact their healthcare provider if they experience signs and symptoms of liver injury. • The FDA's decision was prompted by a postmarketing report of a patient exhibiting elevated liver blood test values and liver injury symptoms after approximately 40 days of treatment.

The FDA has updated the label for Astellas Pharma's Veozah (fezolinetant) to include a warning about the risk of rare but serious liver injury. Veozah is a non-hormonal medication approved for the treatment of moderate to severe hot flashes associated with menopause. The decision follows a postmarketing review of a patient who developed elevated liver blood test values and signs of liver injury after taking Veozah for about 40 days.

Updated Monitoring Guidelines

The updated prescribing information now advises healthcare professionals to conduct more frequent liver blood tests. This includes monthly screenings for the first two months after initiating Veozah, followed by tests at three, six, and nine months. Baseline hepatic testing before starting Veozah remains a requirement. The FDA emphasizes that patients should immediately discontinue Veozah and contact their healthcare provider if they experience symptoms indicative of liver problems, such as fatigue, nausea, vomiting, unusual itching, jaundice, or dark urine.

Clinical Context and Mechanism of Action

Veozah, approved in May 2023, is a neurokinin 3 (NK3) receptor antagonist. It works by blocking the activity of the NK3 receptor, which plays a role in the brain's regulation of body temperature, thereby reducing the frequency and severity of hot flashes. The drug has steadily increased in usage since its approval, with an estimated 28,700 patients receiving Veozah from U.S. outpatient retail pharmacies as of May 2024.

Industry Impact

Despite the new warning, analysts at Jeffries suggest that the updated label may not significantly impact overall demand for Veozah. They noted that while the additional testing requirements will increase the burden on patients, the strengthened label could provide further clarity on the drug's safety profile.

Alternative Treatments

Bayer is also developing a non-hormonal competitor, elinzanetant, a dual NK1 and NK3 receptor inhibitor, for moderate to severe vasomotor symptoms associated with menopause. This highlights the ongoing efforts to address unmet needs in menopause management with non-hormonal therapies.
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Reference News

[1]
Astellas' Hot Flash Drug Veozah Slapped With Another ...
biospace.com · Sep 13, 2024

FDA added a liver injury warning to Astellas Pharma's Veozah, a therapy for hot flashes, after a patient showed liver da...

[2]
FDA Adds Warning About Rare Occurrence of Serious Liver Injury with Use of Veozah (fezolinetant) for Hot Flashes Due to Menopause
drugs.com · Sep 12, 2024

FDA warns Veozah (fezolinetant) for menopausal hot flashes can cause rare, serious liver injury; update includes new liv...

[3]
FDA updates warning for liver injury due to fezolinetant - Contemporary OB/GYN
contemporaryobgyn.net · Sep 14, 2024

FDA warns of rare, serious liver injuries from fezolinetant (Veozah), updating prescribing info to include monthly liver...

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