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Supplementary file 1_A real-world pharmacovigilance study of FDA adverse event reporting system (FAERS) events for etrasimod.docx
Published 2025“…Objective<p>To characterize the post-marketing safety profile of etrasimod using the latest data from the FDA Adverse Event Reporting System (FAERS), and to provide a comparative analysis versus other sphingosine-1-phosphate (S1P) receptor modulators.…”