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Post-marketing pharmacovigilance and FDA Adverse Event Reporting System (FAERS) data capture rare, unexpected reactions
We extended our analysis to a panel of seven GLP-1RAs, including, as well as exendin-4, exendin-F1 and exendin-D3, fatty acid-modified semaglutide 20 and tirzepatide 21 , as well as small molecules orforglipron 22 and danuglipron 23
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That reduction occurred within 48 weeks and exceeded the results of any other drug tested for that condition (Sanyal et al., NEJM 2024)
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