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The report notes the presence of counterfeit Ozempic, the use of non-FDA-approved ingredients such as retatrutide or cagrilintide, and products bypassing regulations by being labeled as not for human consumption. As of July 2024 the most recently issued report the FDA had received over 1,000 reports of adverse events related to compounded semaglutide and compounded tirzepatide

Paired with consistent exercise and healthy eating, the drugs helped her steer clear of diabetes, but she eventually had to stop taking them

Because of these risks, its essential for patients to review the warning label and discuss any concerns with their healthcare provider before starting Ozempic