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A systematic safety assessment of zuranolone: real-world adverse event analysis from the FAERS database.
タグ:
FAERS
2026/1/31
Drug-related suicidal events in children and teenagers: Age-stratified insights from FAERS.
タグ:
FAERS
2026/1/31
Vaccine-associated lupus and related organ involvements: A pharmacovigilance analysis of VAERS database 1990-2025.
タグ:
VAERS
FAERS
2026/1/30
Cardiovascular Adverse Events of JAK versus TNF Inhibitors using the Korean Pharmacovigilance Database.
タグ:
KAERS
FAERS
2026/1/30
Evaluation of Dexmedetomidine-Associated Bradycardia and Related Drug-Drug Interactions Using Electronic Health Record (EHR) and miRNA Target Analysis.
タグ:
FAERS
2026/1/30
Beyond the label: real-world gastrointestinal adverse events associated with vedolizumab – a decade of FAERS pharmacovigilance.
タグ:
FAERS
2026/1/30
Post-marketing safety concerns with trofinetide: a disproportionality analysis of the first therapeutic agent for Rett syndrome based on the FDA adverse event reporting system (FAERS).
タグ:
FAERS
2026/1/30
Disproportionality analysis of satralizumab in FDA adverse event reporting system and Japanese adverse drug event report: a pharmacovigilance study.
タグ:
JADER
FAERS
2026/1/30
Exploring adverse events associated with vosoritide monotherapy: Insights from the FDA Adverse Event Reporting System.
タグ:
FAERS
2026/1/29
Post-marketing safety surveillance of tarlatamab: a real-world pharmacovigilance study based on the FAERS database.
タグ:
FAERS
2026/1/29
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