Epidermal growth factor receptor-targeted agents and paronychia: A US Food and Drug Administration Adverse Event Reporting System-based real-world pharmacovigilance analysis

J Am Acad Dermatol. 2026 Mar 16:S0190-9622(26)00407-X. doi: 10.1016/j.jaad.2026.03.031. Online ahead of print.
No abstract available

Keywords: US FDA adverse event reporting system (FAERS); dermatologic adverse events; epidermal growth factor receptor inhibitors (EGFR); paronychia; pharmacovigilance.