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Post-marketing safety monitoring of tirzepatide: a pharmacovigilance study based on the FAERS database
Safety monitoring of tirzepatide after approval using reports from the FAERS database
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Abstract
Among 25,212 tirzepatide-related adverse drug event reports, 101 significant adverse event signals were identified across 15 system organ classifications.
- Common adverse drug events included nausea (3,030 reports, ROR 5.38) and vomiting (1,147 reports, ROR 3.44).
- Previously unreported adverse drug events included eructation (500 reports, ROR 46.56) and injection site hemorrhage (1,610 reports, ROR 27.8).
- Women reported more injection-site reactions, while men experienced more gastrointestinal issues.
- The median onset time for adverse drug events was 23 days, with an interquartile range of 6 to 90 days.
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