Publication

Identifying biosimilar side effects: Infliximab-dyyb-associated subcorneal pustular dermatosis

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Last modified
  • 05/20/2025
Type of Material
Authors
    Maria Amoreth R Gozo, U.S.S. Anchorage, Naval Base San Diego, United States Navy, San DiegoIviensan F Manalo, Emory UniversityTunisia Cornelius, Emory Decatur Hospital
Language
  • English
Date
  • 2021-06-01
Publisher
  • Elsevier
Publication Version
Copyright Statement
  • © 2020 Published by Elsevier Inc. on behalf of Women's Dermatologic Society.
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 7
Issue
  • 3
Start Page
  • 367
End Page
  • 368
Grant/Funding Information
  • None
Abstract
  • Biologics such as infliximab account for a growing multibillion-dollar industry, treating a myriad of inflammatory conditions ranging from psoriasis to inflammatory bowel disease. As patents for these medications expire, a growing market is surfacing to derive highly similar but more affordable therapies, known as biosimilars (McKinnon and Ward, 2016). Because the approval process of biosimilars does not require the same extensive clinical trial phases as the originators, we highlight that informational gaps exist on the postmarking side effects of biosimilars (Yamauchi et al., 2018). The following case presents an example of a new-onset rash in the setting of initiating biosimilar infliximab-dyyb treatment.
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Research Categories
  • Health Sciences, Medicine and Surgery

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