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ISCHAEMIC ATTACK"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Renal and urinary disorders","sourceVocabulary":"MedDRA 21.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":68,"numEvents":0},{"groupId":"EG001","numAffected":1,"numAtRisk":142,"numEvents":1}],"term":"ACUTE KIDNEY INJURY"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Renal and urinary disorders","sourceVocabulary":"MedDRA 21.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":68,"numEvents":0},{"groupId":"EG001","numAffected":1,"numAtRisk":142,"numEvents":1}],"term":"URINARY RETENTION"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Respiratory, thoracic and mediastinal disorders","sourceVocabulary":"MedDRA 21.0","stats":[{"groupId":"EG000","numAffected":2,"numAtRisk":68,"numEvents":2},{"groupId":"EG001","numAffected":0,"numAtRisk":142,"numEvents":0}],"term":"ACUTE RESPIRATORY FAILURE"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Respiratory, thoracic and 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21.0","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":68,"numEvents":1},{"groupId":"EG001","numAffected":2,"numAtRisk":142,"numEvents":2}],"term":"RESPIRATORY FAILURE"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Skin and subcutaneous tissue disorders","sourceVocabulary":"MedDRA 21.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":68,"numEvents":0},{"groupId":"EG001","numAffected":1,"numAtRisk":142,"numEvents":1}],"term":"SKIN DISCOLOURATION"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA 21.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":68,"numEvents":0},{"groupId":"EG001","numAffected":2,"numAtRisk":142,"numEvents":2}],"term":"DEEP VEIN THROMBOSIS"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA 21.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":68,"numEvents":0},{"groupId":"EG001","numAffected":1,"numAtRisk":142,"numEvents":1}],"term":"HYPOTENSION"}],"timeFrame":"All-cause mortality includes all deaths up to the data cut-off date of 15 August 2019; median time on study was 17.7 months (range: 0.2-20.8) in the placebo arm and 17.5 months (range: 0.1-23.5) in the venetoclax arm. Adverse events are reported from the first dose of study drug up to 30 days after the last dose, to the data cut-off date of 15 August 2019; median duration of treatment was 1.7 months (range: 0.1-20.2) in the placebo arm and 4.1 months (range: 0.0-23.5) in the venetoclax arm."}