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As of July 31, 2025, the agency has received: 605 adverse event reports tied to compounded semaglutide 545 reports tied to compounded tirzepatide These reports include serious reactions such as nausea, vomiting, abdominal pain, constipation, and errors caused by incorrect dosing or mislabeled products
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Statistical analyses included chi-square tests, independent t tests, Kaplan-Meier survival analysis, and calculations of Cohen d for effect sizes
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