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As new products enter the market, competition is expected to intensify, potentially leading to more affordable options for patients

Exenatide was approved by the US FDA in 2005 and by the European Medicines Agency (EMA) in 2006

Compounded drugs aren't reviewed by the FDA for safety or effectiveness before they're sold, and the agency had received more than 455 adverse event reports linked to compounded semaglutide as of early 2025, many involving dosing errors from multidose vials

Stimulation of glucagon-like peptide-1 receptor through exendin-4 preserves myocardial performance and prevents cardiac remodeling in infarcted myocardium

Iodine deficiency causes thyroid disease (3,4)

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