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FDAs 2025 Increase in Warning Letters on Compounded Drug Advertising In recent remarks at the Food and Drug Law Institutes Enforcement, Litigation, and Compliance Conference, the director of the Office of Compliance within FDAs Center for Drug Evaluation and Research's (CDER) noted that 22% of warning letters that CDER issued in fiscal year (FY) 2025 were sent to telehealth platforms and other entities related to claims made regarding compounded drug products, including compounded GLP-1s

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This protocol makes the most sense for individuals who have already completed a cycle of semaglutide or tirzepatide and know they handle GLP-1 receptor activation without severe GI distress

All of that can make GLP-1s very attractive, leading more and more new moms to ask their doctors about starting them

They could have severe side effects from dosing errors." Dr