Pharmacovigilance analysis of orlistat adverse events based on the FDA adverse event reporting system (FAERS) database

Orlistat
DOI: 10.1016/j.heliyon.2024.e34837 Publication Date: 2024-07-18T01:37:23Z
ABSTRACT
Based on the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS) database, we analyzed signals of potential adverse events (AEs) orlistat in real world to provide a reference for its safe clinical use.
SUPPLEMENTAL MATERIAL
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