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FDA Sends Warning Letters to More Than 50 GLP-1 Compounders and Manufacturers
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FDA Issues Warning Letters to 30 Telehealth Companies Over Misleading Compounded GLP-1 RA Marketing
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FDA Escalates Enforcement Against Compounded GLP-1 Marketing
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June 2, 2025: FDA continues to protect Americans from unapproved and contaminated medicine – Partnership for Safe Medicines
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The FDA has issued warning letters to multiple companies marketing compounded Retatrutide, an investigational drug from Eli Lilly still in Phase II trials. While early studies have shown promising weight-loss results, Retatrutide
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GLP-1 prescribing among teens with obesity
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Pharmacovigilance Assessment of Compounded GLP-1 Receptor Agonists: Insights From the FDA Adverse Event Reporting System
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