Postmarketing safety surveillance of adalimumab, secukinumab, and infliximab in hidradenitis suppurativa: an analysis of the FDA adverse events reporting system (FAERS) database
- PMID: 39978679
- DOI: 10.1016/j.jaad.2025.02.031
Postmarketing safety surveillance of adalimumab, secukinumab, and infliximab in hidradenitis suppurativa: an analysis of the FDA adverse events reporting system (FAERS) database
Keywords: FDA adverse event reporting system (FAERS); adalimumab; adverse events; biologics; hidradenitis suppurativa; infliximab; pharmacovigilance; postmarketing surveillance; safety profiling; secukinumab.
Conflict of interest statement
Conflicts of interest Dr Shi is on the board of directors for the Hidradenitis Suppurativa Foundation (HSF), an advisor for the National Eczema Association, is a stock shareholder of Learn Health and has served as an advisory board member, investigator, speaker, and/or received research funding from Sanofi Genzyme, Regeneron, AbbVie, Genentech, Eli Lilly, Novartis, SUN Pharma, LEO Pharma, Pfizer, Incyte, Dermavant, Boehringer Ingelheim, Almirall, Alumis, Aristea Therapeutics, Menlo Therapeutics, Dermira, Burt’s Bees, Galderma, Kiniksa, UCB, Ceraclere, Bain Capital, Target-PharmaSolutions, Castle Bioscience, Altus Lab/cQuell, MYOR, Polyfins Technology, GpSkin and Skin Actives Scientific. Authors Joshi and Saadi and Drs Gawey, Naidoo, Rick, Park, Cogen, Daveluy, and Hsiao have no conflicts of interest to declare.
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