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As of early 2025, the FDA had received more than 455 adverse event reports linked to compounded semaglutide and more than 320 reports associated with compounded tirzepatide, many involving dosing errors from patients self-administering incorrect doses from multidose vials—some of which required hospitalization
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10.1111/acps.12698 [DOI] [PubMed] [Google Scholar] Kondo M., Nakamura Y., Ishida Y., Shimada S
