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Reporting of Drug Reaction with Eosinophilia and Systemic Symptoms from 2002-2019 in the FDA Adverse Event Reporting System (FAERS)

Bluestein, S.B., Yu, R., Stone, C.A. and Phillips, E.J. (2021) Reporting of Drug Reaction with Eosinophilia and Systemic Symptoms from 2002-2019 in the FDA Adverse Event Reporting System (FAERS). The Journal of Allergy and Clinical Immunology: In Practice, 9 (8). 3208-3211.e1.

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Embargoed until May 2022.

Link to Published Version: https://doi.org/10.1016/j.jaip.2021.05.008
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Abstract

Clinical Implications

• Of drug reaction with eosinophilia and systemic symptoms cases identified in the Food and Drug Administration Adverse Event Reporting System, five drugs account for more than 50% of cases and three have actionable HLA risk factors identifying implementation strategies for prevention and earlier diagnosis.

Item Type: Journal Article
Murdoch Affiliation(s): Institute for Immunology and Infectious Diseases
Publisher: Elsevier
Copyright: © 2021 Published by Elsevier Inc. on behalf of the American Academy of Allergy, Asthma & Immunology
URI: http://researchrepository.murdoch.edu.au/id/eprint/60956
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