Tag: Pharmacovigilance

Acute Cholecystitis Associated With the Use of Glucagon-Like Peptide-1 Receptor Agonists Reported to the US Food and Drug Administration

This 2022 pharmacovigilance study analyzed FDA Adverse Event Reporting System (FAERS) data to assess the association between GLP-1 receptor agonists (GLP-1 RAs) and acute cholecystitis. The analysis revealed a notable number of reports linking GLP-1 RAs, such as liraglutide and semaglutide, to cases of acute cholecystitis. The proposed mechanism involves

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The cardiovascular safety of antiobesity drugs—analysis of signals in the FDA Adverse Event Report System Database

This 2020 pharmacovigilance study analyzed data from the FDA Adverse Event Reporting System (FAERS) to assess cardiovascular safety signals associated with antiobesity medications. The researchers focused on drugs including lorcaserin, phentermine, orlistat, and naltrexone/bupropion. Findings indicated that lorcaserin was associated with reports of valvulopathy and cardiac disorders, while phentermine was

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