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
AUTHORS (13)
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
Coming soon ....
REFERENCES (86)
CITATIONS (3)
EXTERNAL LINKS
PlumX Metrics
RECOMMENDATIONS
FAIR ASSESSMENT
Coming soon ....
JUPYTER LAB
Coming soon ....