Post-market surveillance data demonstrate high mortality associated with enfortumab vedotin skin toxicity, not worsened by immune checkpoint inhibitors or corticosteroids - 26/11/25

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Key words : adverse effects, adverse events, descriptive study, enfortumab vedotin, Enfortumab, EV, FAERS, FDA adverse event reporting database, FDA adverse event reporting system, oncodermatology, Padcev, post-market, post-marketing, rash, SDRIFE, side effects, SJS, skin toxicity, Stevens–Johnson syndrome, supportive oncodermatology, surveillance, symmetrical drug-related intertriginous and flexural eruption, TEN, toxic epidermal necrolysis, urothelial cancer
| Author Kilton and Dr Wei contributed equally to this work. |
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| Funding sources: None. |
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| Patient consent: Not applicable. |
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| IRB approval status: No institutional review board approval was required for this study. |
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| No data from this study has been previously published or presented elsewhere. The study was presented as a poster by MMK at University of Nebraska's Medical Student Research Showcase on August 22, 2025. The abstract and poster are not published online and we do not expect them to be. |
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