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Comparative analysis of adverse event reporting signals between Satralizumab and Inebilizumab in neuromyelitis optica spectrum disorder: A pharmacovigilance study using the FDA Adverse Event Reporting System.
タグ:
FAERS
2026/2/26
Adverse drug events and toxicological mechanisms of esketamine: a study based on US Food and Drug Administration Adverse Event Reporting System and network toxicology analysis.
タグ:
FAERS
2026/2/26
Drugs Associated with Pediatric Cataracts: A Real-World Pharmacovigilance Study.
タグ:
FAERS
2026/2/27
Analysis of adverse event reporting with casimersen: a pharmacovigilance study based on the United States food and drug administration adverse event reporting system database.
タグ:
FAERS
2026/2/26
Thromboembolic events with olanzapine: a systematic review integrating meta-analysis and FAERS database.
タグ:
FAERS
2026/2/27
Evaluating the real-world safety of cholestyramine for the treatment of hyperlipidemia: disproportionality analysis of FAERS data.
タグ:
FAERS
2026/2/27
Real-world safety of voretigene neparvovec: a disproportionality analysis for signal detection using the FAERS database.
タグ:
FAERS
2026/2/27
Real-world disproportionality analysis of trabectedin using the United States food and drug administration adverse event reporting system.
タグ:
FAERS
2026/2/27
Assessing the real-world drug safety of sevelamer for hyperphosphatemia: Insights from a comprehensive analysis of the FDA adverse event reporting system (FAERS) database.
タグ:
FAERS
2026/2/28
A real-world pharmacovigilance study of bempedoic acid plus ezetimibe fixed-dose combination based on the FDA FAERS database.
タグ:
FAERS
2026/2/28
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