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Bile acids as candidate therapies for multiple sclerosis: inverse signal analysis using the FDA adverse event reporting system and preclinical validation.
タグ:
FAERS
2026/3/15
Ocular adverse events associated with aflibercept and faricimab: a population-based pharmacovigilance study.
タグ:
FAERS
2026/3/16
Risk factors for drug-related ischemic stroke: an analysis of the FDA adverse event reporting system (FAERS).
タグ:
FAERS
2026/3/16
Evaluation of the real-world safety of eptifibatide in the treatment of ARDS: results of a disproportionality analysis of FAERS data.
タグ:
FAERS
2026/3/16
MSAT: a FAERS-informed heterogeneous graph neural network for pharmacovigilance prediction of Chinese materia medica-associated adverse drug reactions.
タグ:
FAERS
2026/3/16
Post-marketing safety of CGRP monoclonal antibodies and gepants: A systematic review of spontaneous reporting system data.
タグ:
VigiBase
EudraVigilance
FAERS
2026/3/16
EGFR-targeted agents and paronychia: a FAERS-based real-world pharmacovigilance analysis.
タグ:
FAERS
2026/3/19
Real-world safety of satralizumab in neuromyelitis optica spectrum disorder: a FAERS-based risk stratification study.
タグ:
FAERS
2026/3/18
Signal detection of drug-induced esophageal ulcer across 20 years of real-world study: Focus on 49 high-risk medicines.
タグ:
FAERS
2026/3/17
Safety Assessment of Glucagon-Like Peptide 1 Receptor Agonists Based on the FAERS Database: Focus on Tumorigenic Risk in Subpopulations.
タグ:
FAERS
2026/3/20
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