1995
DOI: 10.1056/nejm199512143332404
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Medication Use and the Risk of Stevens–Johnson Syndrome or Toxic Epidermal Necrolysis

Abstract: The use of antibacterial sulfonamides, anticonvulsant agents, oxicam NSAIDs, allopurinol, chlormezanone, and corticosteroids is associated with large increases in the risk of Stevens-Johnson syndrome or toxic epidermal necrolysis. But for none of the drugs does the excess risk exceed five cases per million users per week.

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Cited by 1,239 publications
(584 citation statements)
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References 34 publications
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“…Patient developed TEN about 6 weeks after initiation of ATT which manifested in the classic form. A delayed onset could be attributed to a short course of systemic steroids on initiation of ATT [4]. Management in ICU with burns protocol of fluid and electrolyte replenishment and intravenous antibiotics was beneficial to the patient.…”
Section: Discussionmentioning
confidence: 99%
“…Patient developed TEN about 6 weeks after initiation of ATT which manifested in the classic form. A delayed onset could be attributed to a short course of systemic steroids on initiation of ATT [4]. Management in ICU with burns protocol of fluid and electrolyte replenishment and intravenous antibiotics was beneficial to the patient.…”
Section: Discussionmentioning
confidence: 99%
“…A limited number of drugs are associated with a high risk for SJS and TEN: several antiepileptic agents, especially carbamazepine, phenytoin, phenobarbital and lamotrigine, antibacterial sulfonamides, anti-inflammatory drugs of the oxicam family, allopurinol and the antiretroviral agent nevirapine. 1,2 Although the pathophysiology of SJS and TEN remains largely unknown, previous work suggests an immune mechanism involving a drug-dependent cytotoxic cell response against epidermal cells. Cytokines like TNFa and Fas ligand (FasL) may play a role in the final apoptosis of the keratinocytes, but the initial events triggering the adverse reaction remain to be identified.…”
Section: Introductionmentioning
confidence: 99%
“…Case histories were [1][2][3][4]. We have previously published the results of a population-based cohort study providing quantitative inforreviewed by the authors who gave strong consideration to the clinical diagnoses made by the physicians who cared for mation on the risk of co-trimoxazole-associated serious blood and skin disorders using data from the General Practice the patients.…”
mentioning
confidence: 99%