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The Medication Risk of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Asians: The Major Drug Causality and Comparison With the US FDA Label.
Wang, Yu-Hsin; Chen, Chun-Bing; Tassaneeyakul, Wichittra; Saito, Yoshiro; Aihara, Michiko; Choon, Siew Eng; Lee, Haur Yueh; Chang, Mimi Mee; Roa, Francisca D; Wu, Cheng-Wei; Zhang, Jing; Nakkam, Nontaya; Konyoung, Parinya; Okamoto-Uchida, Yoshimi; Cheung, Christina Man-Tung; Huang, Jin-Wen; Ji, Chao; Cheng, Bo; Hui, Rosaline Chung-Yee; Chu, Chia-Yu; Chen, Yi-Ju; Wu, Ching-Ying; Hsu, Chao-Kai; Chiu, Tsu-Man; Huang, Yu-Huei; Lu, Chun-Wei; Yang, Chin-Yi; Lin, Yi-Ting; Chi, Min-Hui; Ho, Hsin-Chun; Lin, Jing-Yi; Yang, Chih-Hsun; Chang, Ya-Ching; Su, Shih-Chi; Wang, Chuang Wei; Fan, Wen-Lang; Hung, Shuen-Iu; Chung, Wen-Hung.
Afiliación
  • Wang YH; Chang Gung Memorial Hospital, Linkou, Taiwan.
  • Chen CB; Department of Dermatology, Drug Hypersensitivity Clinical and Research Center, Chang Gung Memorial Hospital, Taipei, Linkou, and Keelung, Taiwan.
  • Tassaneeyakul W; Chang Gung Memorial Hospital, Linkou, Taiwan.
  • Saito Y; Department of Dermatology, Drug Hypersensitivity Clinical and Research Center, Chang Gung Memorial Hospital, Taipei, Linkou, and Keelung, Taiwan.
  • Aihara M; College of Medicine, Chang Gung University, Taoyuan, Taiwan.
  • Choon SE; Graduate Institute of Clinical Medical Sciences, College of Medicine, Chang Gung University, Taoyuan, Taiwan.
  • Lee HY; Whole-Genome Research Core Laboratory of Human Diseases, Chang Gung Memorial Hospital, Keelung, Taiwan.
  • Chang MM; Chang Gung Immunology Consortium, Chang Gung Memorial Hospital and Chang Gung University, Taoyuan, Taiwan.
  • Roa FD; Chang Gung Memorial Hospital, Xiamen, China.
  • Wu CW; Department of Pharmacology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
  • Zhang J; Division of Medicinal Safety Science, National Institute of Health Sciences, Japan.
  • Nakkam N; Department of Environmental Immuno-Dermatology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Konyoung P; Hospital Sultanah Aminah Johor Bahru, Clinical School of Medicine and Health Sciences, Monash University Malaysia.
  • Okamoto-Uchida Y; Department of Dermatology, Singapore General Hospital, Singapore.
  • Cheung CM; Duke-NUS medical school, Singapore.
  • Huang JW; Division of Dermatology, Department of Medicine and Therapeutics, Prince of Wales Hospital, the Chinese University of Hong Kong.
  • Ji C; University of the Philippines-Philippine, General Hospital, Manila, Philippines.
  • Cheng B; Chang Gung Memorial Hospital, Kaohsiung, Taiwan.
  • Hui RC; Department of Dermatology, the First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, China.
  • Chu CY; Department of Pharmacology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
  • Chen YJ; Pharmacy Unit, Udon Thani Hospital, Udon Thani, Thailand.
  • Wu CY; Division of Medicinal Safety Science, National Institute of Health Sciences, Japan.
  • Hsu CK; Division of Dermatology, Department of Medicine and Therapeutics, Prince of Wales Hospital, the Chinese University of Hong Kong.
  • Chiu TM; Department of Dermatology, the First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, China.
  • Huang YH; Department of Dermatology, the First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, China.
  • Lu CW; Department of Dermatology, the First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, China.
  • Yang CY; Chang Gung Memorial Hospital, Linkou, Taiwan.
  • Lin YT; Department of Dermatology, Drug Hypersensitivity Clinical and Research Center, Chang Gung Memorial Hospital, Taipei, Linkou, and Keelung, Taiwan.
  • Chi MH; College of Medicine, Chang Gung University, Taoyuan, Taiwan.
  • Ho HC; Department of Dermatology, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.
  • Lin JY; Department of Dermatology, Taichung Veterans General Hospital, National Yang Ming University, Taichung, Taiwan.
  • Yang CH; Department of dermatology, municipal Ta-Tong hospital, Kaohsiung medical university, Taiwan.
  • Chang YC; Department of Dermatology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
  • Su SC; Department of Dermatology, Changhua Christian Hospital, Changhua, Taiwan.
  • Wang CW; Chang Gung Memorial Hospital, Linkou, Taiwan.
  • Fan WL; Department of Dermatology, Drug Hypersensitivity Clinical and Research Center, Chang Gung Memorial Hospital, Taipei, Linkou, and Keelung, Taiwan.
  • Hung SI; College of Medicine, Chang Gung University, Taoyuan, Taiwan.
  • Chung WH; Chang Gung Memorial Hospital, Linkou, Taiwan.
Clin Pharmacol Ther ; 105(1): 112-120, 2019 01.
Article en En | MEDLINE | ID: mdl-29569740
Specific ethnic genetic backgrounds are associated with the risk of Stevens-Johnson syndrome / toxic epidermal necrolysis (SJS/TEN) especially in Asians. However, there have been no large cohort, multiple-country epidemiological studies of medication risk related to SJS/TEN in Asian populations. Thus, we analyzed the registration databases from multiple Asian countries who were treated during 1998-2017. A total 1,028 SJS/TEN cases were identified with the algorithm of drug causality for epidermal necrolysis. Furthermore, those medications labeled by the US Food and Drug Administration (FDA) as carrying a risk of SJS/TEN were also compared with the common causes of SJS/TEN in Asian countries. Oxcarbazepine, sulfasalazine, COX-II inhibitors, and strontium ranelate were identified as new potential causes. In addition to sulfa drugs and beta-lactam antibiotics, quinolones were also a common cause. Only one acetaminophen-induced SJS was identified, while several medications (e.g., oseltamivir, terbinafine, isotretinoin, and sorafenib) labeled as carrying a risk of SJS/TEN by the FDA were not found to have caused any of the cases in the Asian countries investigated in this study.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: United States Food and Drug Administration / Síndrome de Stevens-Johnson / Pueblo Asiatico / Etiquetado de Medicamentos Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: Clin Pharmacol Ther Año: 2019 Tipo del documento: Article País de afiliación: Taiwán

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: United States Food and Drug Administration / Síndrome de Stevens-Johnson / Pueblo Asiatico / Etiquetado de Medicamentos Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: Clin Pharmacol Ther Año: 2019 Tipo del documento: Article País de afiliación: Taiwán
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