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. 2023 Jul 14;78(11):2980–2993. doi: 10.1111/all.15814

TABLE 1.

Study cohort HLA and drug hypersensitivity information.

Study ID HLA‐B ALP exposure cADR Collection date Time post‐reaction
CU001 58:01 No No 13/10/2010
CU002 58:01 Yes SJS 29/09/2010 4 years
CU003 58:01 Yes SJS 27/09/2010 6 years
CU004 58:01 No No 13/10/2010
CU005 58:01 Yes TEN 28/09/2010 5 years
CU006 58:01 Yes SJS 10/04/2010 7 years
AP012 57:01, 58:01 No No 23/07/2014
AP013 15:01, 58:01 No No 24/07/2014
AP014 41:01, 58:01 No No 30/07/2014
AP015 40:06, 58:01 No No 31/07/2014
AP016 27:04, 58:01 No No 13/08/2014
AP018 39:24, 58:01 No No 27/08/2014
AP025 07:02, 58:01 No No 22/09/2014
AP027 15:02, 58 No No 30/09/2014
AP101 44, 58 No No 12/03/2014
AP105 7, 8 No No 20/03/2014
AP108 14:01, 51:01 No No 31/03/2014
AP111 44, 57 No No 18/06/2014

Note: Patients are denoted as CU and healthy participants are denoted as AP. For CU patients, it is unknown whether HLA‐B*58:01 is homozygous or heterozygous.

Abbreviations: cADR, cutaneous adverse drug reaction; SJS, Stevens–Johnson syndrome; TEN, toxic epidermal necrolysis.