Implications for pharmaceutical care in DRESS syndrome
DOI:
https://doi.org/10.36557/2674-8169.2026v8n4p581-593Keywords:
DRESS syndrome; drug hypersensitivity; pharmacovigilance; pharmaceutical care.Abstract
Objective: to synthesize the evidence on the main drugs implicated in DRESS syndrome and reorganize it into a care flow focused on pharmaceutical practice. Methods: narrative review with an applied clinical perspective, prioritizing systematic reviews, cohorts, multicenter studies, pharmacogenetic investigations, and international consensus documents on drug-induced DRESS. Results: evidence indicates that allopurinol, aromatic anticonvulsants, lamotrigine, vancomycin, sulfonamides, dapsone, and antituberculosis regimens account for a relevant proportion of cases and severe outcomes. The highest-risk window usually occurs between two and eight weeks after treatment initiation, although antibacterials and iodinated contrast agents may trigger earlier presentations. For pharmacists, early recognition of diffuse rash, fever, facial edema, eosinophilia, jaundice, dyspnea, and hepatic or renal deterioration should prompt urgent communication with the care team, chronological medication review, and clear documentation of the suspected reaction. Conclusion: pharmacists play a strategic role in risk stratification, patient education, early treatment monitoring, prevention of re-exposure, and pharmacovigilance, and should incorporate a standardized assessment and referral flow for patients exposed to higher-risk drugs
Downloads
References
BRÜGGEN, M.-C. et al. Management of adult patients with drug reaction with eosinophilia and systemic symptoms: a Delphi-based international consensus. JAMA Dermatology, Chicago, v. 160, n. 1, p. 37-44, 2024. Disponível em: https://doi.org/10.1001/jamadermatol.2023.4450.
CACOUB, P. et al. The DRESS syndrome: a literature review. The American Journal of Medicine, New York, v. 124, n. 7, p. 588-597, 2011. Disponível em: https://doi.org/10.1016/j.amjmed.2011.01.017.
CALLE, A. M. et al. DRESS syndrome: a literature review and treatment algorithm. World Allergy Organization Journal, [s. l.], v. 16, n. 3, e100673, 2023. Disponível em: https://doi.org/10.1016/j.waojou.2022.100673.
JUNG, H. Y. et al. Prevalence and clinical features of drug reactions with eosinophilia and systemic symptoms syndrome caused by antituberculosis drugs: a retrospective cohort study. Allergy, Asthma & Immunology Research, Seoul, v. 11, n. 1, p. 90-103, 2019. Disponível em: https://doi.org/10.4168/aair.2019.11.1.90.
KARDAUN, S. H. et al. Drug reaction with eosinophilia and systemic symptoms (DRESS): an original multisystem adverse drug reaction. Results from the prospective RegiSCAR study. British Journal of Dermatology,
KO, T.-M. et al. Use of HLA-B*58:01 genotyping to prevent allopurinol-induced severe cutaneous adverse reactions in Taiwan: national prospective cohort study. BMJ, London, v. 351, h4848, 2015. Disponível em: https://doi.org/10.1136/bmj.h4848.
KROSHINSKY, D.; CARDONES, A. R.; BLUMENTHAL, K. G. Drug reaction with eosinophilia and systemic symptoms. New England Journal of Medicine, Boston, v. 391, n. 23, p. 2242-2254, 2024. Disponível em: https://doi.org/10.1056/NEJMra2204547.
LIANG, C. et al. Fatal outcome related to drug reaction with eosinophilia and systemic symptoms: a disproportionality analysis of FAERS database and a systematic review of cases. Frontiers in Immunology, Lausanne, v. 15, 1490334, 2024. Disponível em: https://doi.org/10.3389/fimmu.2024.1490334.
MUSHIRODA, T. et al. Association of HLA-A*31:01 screening with the incidence of carbamazepine-induced cutaneous adverse reactions in a Japanese population. JAMA Neurology, Chicago, v. 75, n. 7, p. 842-849, 2018. Disponível em: https://doi.org/10.1001/jamaneurol.2018.0278.
SATO, T. et al. Real-world evidence of population differences in allopurinol-related severe cutaneous adverse reactions in East Asians: a population-based cohort study. Clinical and Translational Science, Alexandria, v. 14, n. 3, p. 1002-1014, 2021. Disponível em: https://doi.org/10.1111/cts.12964.
SATAPORNPONG, P. et al. HLA-B*13:01 is a predictive marker of dapsone-induced severe cutaneous adverse reactions in Thai patients. Frontiers in Immunology, Lausanne, v. 12, 661135, 2021. Disponível em: https://doi.org/10.3389/fimmu.2021.661135.
SIM, D. W. et al. Variation of clinical manifestations according to culprit drugs in DRESS syndrome. Pharmacoepidemiology and Drug Safety, Chichester, v. 28, n. 6, p. 840-848, 2019. Disponível em: https://doi.org/10.1002/pds.4774.
SORIA, A. et al. Drug reaction with eosinophilia and systemic symptoms may occur within 2 weeks of drug exposure: a retrospective study. Journal of the American Academy of Dermatology, St. Louis, v. 82, n. 3, p. 606-611, 2020. Disponível em: https://doi.org/10.1016/j.jaad.2019.09.036.
ZHANG, F.-R. et al. HLA-B*13:01 and the dapsone hypersensitivity syndrome. New England Journal of Medicine, Boston, v. 369, n. 17, p. 1620-1628, 2013. Disponível em: https://doi.org/10.1056/NEJMoa1213096.
ZIEBART, R. L. et al. Vancomycin-associated drug-induced hypersensitivity syndrome: a retrospective cohort study. Journal of the American Academy of Dermatology, St. Louis, v. 91, n. 5, p. 1008-1011, 2024. Disponível em: https://doi.org/10.1016/j.jaad.2024.07.1471.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2026 Cláudio Luiz Ferreira Júnior, Lidiane Lopes Moreira

This work is licensed under a Creative Commons Attribution 4.0 International License.
Authors are copyright holders under a CCBY 4.0 license.



