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.

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