FDA · Safety alert

FDA alerts on dosing errors involving compounded injectable semaglutide

FDA reported adverse events, including some requiring hospitalization, associated with dosing errors involving compounded injectable semaglutide and described risks tied to varying concentrations, vial-and-syringe measurement, and unit conversion.

Safety communication legal stageJul 26, 2024 record dateUnited States jurisdiction
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Record status

Active safety communication

Agency
U.S. Food and Drug Administration
Action
Compounding risk alert
Stage
Safety communication
Last verified
Jul 10, 2026

Source-backed timeline

Status history

  1. Safety alert publishedSource

Editorial boundary: Peptide Report summarizes the public source and preserves its procedural stage. This page does not convert an allegation, proposal, advisory discussion, or warning into a final legal conclusion.

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