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Pharmacovigilance Assessment of Compounded GLP-1 Receptor Agonists: Insights From the FDA Adverse Event Reporting System
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Trends In FDA FY 2025 Warning Letters
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Report: FDA must enforce rules on compounded GLP-1s
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Article: Brazilian Clinics and the False Equivalence of Compounded GLP-1 Drugs: ANVISA should follow FDA
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FDA Issues Warnings Against Illegal GLP-1 Marketing
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CDER Warning Letters Jump 50% in FY 2025 — What That Means for Industry
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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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