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Safety profile of faricimab: a multi-source pharmacovigilance analysis using FAERS and JADER.
タグ:
JADER
FAERS
2025/4/13
Drug-induced Guillain-Barre Syndrome: a disproportionality analysis based on the US FDA adverse event reporting system.
タグ:
VAERS
FAERS
2025/4/12
Comprehensive analysis of adverse drug reactions associated with teduglutide: post-marketing insights and safety implications.
タグ:
FAERS
2025/4/12
Variations in adverse events associated with different infusion modalities of parenteral nutrition: A pharmacovigilance study.
タグ:
FAERS
2025/4/16
Adverse events of concomitant use of immune checkpoint inhibitors and metformin or statin: an observational, retrospective disproportionality analysis.
タグ:
FAERS
2025/4/15
A disproportionality analysis of interstitial lung disease associated with drug therapy in spontaneous adverse event reports.
タグ:
FAERS
2025/4/15
Safety assessment of ripretinib: a real-world adverse event analysis from the food and drug administration adverse event reporting system.
タグ:
FAERS
2025/4/15
Comparative safety analysis of baloxavir marboxil and oseltamivir based on the FAERS database.
タグ:
FAERS
2025/4/17
Infection-related adverse events comparison of bortezomib, carfilzomib and ixazomib: a pharmacovigilance study based on FAERS.
タグ:
FAERS
2025/4/17
A real-world disproportionality analysis of FDA adverse event reporting system (FAERS) events for lecanemab.
タグ:
FAERS
2025/4/17
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