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Sex-stratified disproportionality signals of adverse events with allopurinol and febuxostat: a retrospective pharmacovigilance analysis of FAERS and EudraVigilance.
タグ:
EudraVigilance
FAERS
2026/9/30
Peripheral and central nervous system toxicities of Bruton tyrosine kinase Inhibitors: a real-world pharmacovigilance study.
タグ:
FAERS
2026/9/30
Temporal changes in auditory adverse event reporting in the U.S. vaccine adverse event reporting system associated with the COVID-19 vaccine rollout: an interrupted time series analysis with negative control evaluation.
タグ:
VAERS
FAERS
2026/9/30
Unsupervised machine learning for multi-system adverse event pattern detection in pharmacovigilance: A proof-of-concept analysis of fluoroquinolone reports in FAERS.
タグ:
CVAR
FAERS
2026/9/30
Post-Marketing Safety of the Menin Inhibitor Revumenib: A Bayesian Disproportionality Analysis of a National Database.
タグ:
FAERS
2026/9/30
Serious and Non-serious Hepatitis Reports in the U.S. Vaccine Adverse Event Reporting System, 1990-2026: A Cross-Sectional Analysis.
タグ:
VAERS
FAERS
2026/10/1
Age-stratified safety signal mining of ADHD medications in pediatric populations using the FAERS database (2014-2024): a pharmacovigilance study using multi-method disproportionality analysis.
タグ:
FAERS
2026/10/1
Distinct renal adverse event profiles among CDK4/6 inhibitors: a comparative pharmacovigilance analysis.
タグ:
FAERS
2026/10/2
Pharmacovigilance signal detection of rilonacept using FAERS with exploratory Mendelian randomization analysis.
タグ:
FAERS
2026/10/1
Safety assessment of ambrisentan based on the FDA Adverse Event Reporting System.
タグ:
FAERS
2026/10/2
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