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Safety of infliximab and adalimumab in pediatric inflammatory bowel diseases: a disproportionality analysis from the FAERS database.
タグ:
FAERS
2025/8/8
A pharmacovigilance study of vortioxetine based on data from the FDA adverse event reporting system.
タグ:
FAERS
2025/8/8
Safety assessment of Osilodrostat: The adverse event analysis based on FAERS database by means of disproportionality analysis.
タグ:
FAERS
2025/8/7
Real-world pharmacovigilance assessment of hepatotoxicity risk with HER2-Targeted drugs using FAERS database analysis.
タグ:
FAERS
2025/8/7
Torsade de Pointes and QT Prolongation Among Antifungal Triazoles: A Real-World, Retrospective, Observational, Pharmacovigilance Analysis of the FDA Adverse Event Reporting System (FAERS) Database.
タグ:
FAERS
2025/8/6
A real-world pharmacovigilance study of Certolizumab pegol based on FAERS database.
タグ:
FAERS
2025/8/6
Beyond the Prostate: A Visionary Study on Ocular Impacts of Benign Prostatic Hyperplasia Drugs.
タグ:
FAERS
2025/8/6
Infective pneumonia following the use of tumor necrosis factor-alpha inhibitors in inflammatory bowel disease patients: A real-world disproportionality analysis of the FDA Adverse Event Reporting System (FAERS) database.
タグ:
FAERS
2025/8/5
Cardiac Adverse Events Associated With Elotuzumab: A Disproportionality Analysis Using FDA Adverse Event Reporting System.
タグ:
FAERS
2025/8/4
Anaphylaxis to Penicillin: Harvesting Insights From the Food and Drug Administration’s Adverse Event Reporting System.
タグ:
FAERS
2025/8/3
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