2018The Journal of Allergy and Clinical Immunology In PracticeOpen access

Drug-induced Stevens-Johnson syndrome and toxic epidermal necrolysis: Proportion and determinants of underreporting to pharmacovigilance

G. Chaby, Bénédicte Lebrun‐Vignes, Cynthia Haddad, F. Hémery, S. Oro, Nicolas de Prost, P. Wolkenstein, O. Chosidow, L. Fardet

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Abstract

Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are immunologically mediated severe cutaneous adverse reactions (SCARs) secondary in most cases to the administration of a drug.1 Reporting to national pharmacovigilance databases is an important source of information on adverse drug reactions (ADRs). In France, health care professionals, including physicians and pharmacists, are legally required to report to pharmacovigilance all suspected ADRs. However, it has been estimated that only 5% to 15% of serious ADRs are reported to pharmacovigilance, even though very little accurate data are available.

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What this paper is about

Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are immunologically mediated severe cutaneous adverse reactions (SCARs) secondary in most cases to the administration of a drug.1 Reporting to national pharmacovigilance databases is an important source of information on adverse drug reactions (ADRs). In France, health care professionals, including physicians and pharmacists, are legally required to report to pharmacovigilance all suspected ADRs. However, it has been estimated that only 5% to 15% of serious ADRs are reported to pharmacovigilance, even though very little accurate data are available.

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Available abstract

Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are immunologically mediated severe cutaneous adverse reactions (SCARs) secondary in most cases to the administration of a drug.1 Reporting to national pharmacovigilance databases is an important source of information on adverse drug reactions (ADRs). In France, health care professionals, including physicians and pharmacists, are legally required to report to pharmacovigilance all suspected ADRs. However, it has been estimated that only 5% to 15% of serious ADRs are reported to pharmacovigilance, even though very little accurate data are available.

Key concepts: Toxic epidermal necrolysis, Pharmacovigilance, Medicine, Drug reaction, Adverse drug reaction, Dermatology, Drug, Scars

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