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doi: 10.1097/bor.0000000000000414 31 BalevicSJWeinerDClowseMEBEudyAMMaharajARHornikCPet al

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Over 10,000 semaglutide-related adverse events were reported to the FDAs Adverse Event Reporting System (FAERS) a database that contains adverse event reports, medication error reports and product quality complaints submitted to FDA through the 4th quarter of 2021

Administering the medication requires a subcutaneous (under-the-skin) injection in your upper arm, abdomen, or thigh once weekly

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