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FDA pharmacovigilance review of FAERS reports for compounded GLP-1s has documented dosing errors, inadvertent overdoses, and product quality concerns linked specifically to the regulatory gap between compounded and brand-name product (Hoffman et al., 2025)

This study was presented at the European Academy of Dermatology and Venereology Congress 2025 in Paris, France

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Nutrients, 12 (4), 1181

Association of Obesity with Multiple Sclerosis Risk and Response to First-Line Disease Modifying Drugs in Children

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