fda compounding semaglutide warning letters october 2025 glp-1 Pharmacovigilance Assessment of Compounded GLP-1 Receptor Agonists: Insights From the FDA Adverse Event Reporting System From Crackdown to Collaboration: FDA

They are not manufactured under pharmaceutical-grade conditions, are not FDA-regulated, and are not intended for human use

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Ask for documentation of their sterile compounding protocols and recent inspection results

The contrast is stark

A clinician may need to consider the wider health picture instead of assuming the medication is the sole cause

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