Real-world pharmacovigilance analysis and cross-database consistency assessment of resmetirom-related adverse events using FAERS and VigiAccess
Objective This study aimed to characterize the post-marketing safety profile and potential adverse event signals of resmetirom using the FAERS and VigiAccess databases. Methods FAERS reports from the quarter of initial United States approval through 2026Q1 were analyzed. After deduplication, DEMO, DRUG, REAC, THER, and...