fda semaglutide news The sent a warning letter to the maker of Ozempic and Wegovy over unreported potential GLP-1 side effects. Here's what to know FDA Warns on Certain Forms

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Below the black-box warning, potential risks appear in descending order in sections titled Contraindications, Warnings and Precautions, and Adverse Reactions. 4 The FDA issues black-box warnings either during drug development, to take effect upon approval of a new agent, or (more commonly) based on post-marketing safety information, 5 which the FDA continuously gathers from reports by patients, clinicians, and industry

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tirzepatide), or flag individuals who may need closer monitoring

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Wegovy is not suitable for everyone