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Abstract
The evaluation of adverse event reporting signals for four drugs shows a rising concern about their pancreatic and biliary safety.
- Glucagon-like peptide-1 receptor agonists (GLP-1RAs) include liraglutide, semaglutide, tirzepatide, and dulaglutide.
- The study analyzed data from the US Food and Drug Administration Adverse Event Reporting System (FAERS).
- Concerns regarding pancreatic and biliary safety are associated with the use of these GLP-1RAs.
- Increased reporting of adverse events may indicate a growing awareness or incidence of related safety issues.
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