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Novo Nordisk and Hims & Hers Partner to Expand Semaglutide Access
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The FDA issued a warning letter to Novo Nordisk for failing to report and investigate potentially serious side effects associated with its popular GLP-1 medications. https://www.medpagetoday.com/publichealthpolicy/fdageneral/120262
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Your diabetic patient on semaglutide develops NAION. Do you stop the drug?, The EMA ( European Medicines Agency) says yes — in June 2025 it labeled NAION a very rare side effect of semaglutide and
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Meeting highlights from the Pharmacovigilance Risk Assessment Committee ( PRAC) 13-16 January 2025
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