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Antiepileptic drugs and foetal disorders: analysis of 20-year data from the pharmacovigilance center.
タグ:
FAERS
2025/3/13
Signal mining and analysis of ripretinib adverse events: a real-world pharmacovigilance analysis based on the FAERS database.
タグ:
FAERS
2025/3/13
Characterizing Cardiotoxicity of FDA-Approved Soft Tissue Sarcoma Targeted Therapies and Immune Checkpoint Inhibitors: A Systematic Review.
タグ:
FAERS
2025/3/13
Off-the-Shelf Large Language Models for Causality Assessment of Individual Case Safety Reports: A Proof-of-Concept with COVID-19 Vaccines.
タグ:
VAERS
FAERS
2025/3/13
Analysis and mining of Dupilumab adverse events based on FAERS database.
タグ:
FAERS
2025/3/13
Mining and analysis of amphotericin B adverse reaction signals: a real-world study based on the FAERS database.
タグ:
FAERS
2025/3/12
Post-marketing safety of elacestrant in breast cancer: a pharmacovigilance investigation using the FDA adverse event reporting system.
タグ:
FAERS
2025/3/12
Post-market safety profile of cefiderocol: a real-world pharmacovigilance exploratory analysis based on U.S. FDA adverse event reporting system (FAERS).
タグ:
FAERS
2025/3/12
Drug-associated gingival disorders: a retrospective pharmacovigilance assessment using disproportionality analysis.
タグ:
VAERS
FAERS
2025/3/12
The real-world safety profile of sertraline: Pharmacovigilance analysis of the FAERS database.
タグ:
FAERS
2025/3/12
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