Beyond the label: real-world gastrointestinal adverse events associated with vedolizumab – a decade of FAERS pharmacovigilance

Background: Vedolizumab is a gut-selective biologic widely used for inflammatory bowel disease (IBD). While randomized controlled trials (RCTs) provide initial safety profiles, real-world pharmacovigilance data are crucial for identifying a broader spectrum of adverse events (AEs), including rare or underrecognized associations. This study aimed to comprehensively characterize the real-world reporting frequency and characteristics of gastrointestinal AEs associated with vedolizumab using spontaneous reporting data. Methods: We analyzed 59,976 vedolizumab-related individual case safety reports from the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS) database, covering the period from Q1 2014 to Q4 2024. After meticulous exclusion of IBD diagnostic terms, 17,943 mentions of vedolizumab-associated gastrointestinal AEs were included. Disproportionality analysis, employing reporting odds ratios (ROR) with a threshold of ≥20 cases and a 95% confidence interval lower bound >1, was performed to detect significant signals. Descriptive analyses, time-to-onset (TTO) analysis, and a semi-quantitative clinical relevance assessment system were also utilized. Results: Disproportionality analysis identified 95 significant gastrointestinal AE preferred terms (PTs). Common and strongly signaled events included diarrhea, abdominal pain, haematochezia, and frequent bowel movements. Notably, 70 of these 95 significant PTs (73.7%) are not explicitly listed in the current vedolizumab drug label, suggesting potential novel or underrecognized associations. Most reported AEs were serious (90.09%). Analysis of demographic data revealed significant differences in the proportion of serious reports across gender, weight, and age groups. Males (91.44%) and patients in the