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disorders","sourceVocabulary":"24.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":176},{"groupId":"EG001","numAffected":0,"numAtRisk":180}],"term":"Pruritus"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Skin and subcutaneous tissue disorders","sourceVocabulary":"24.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":176},{"groupId":"EG001","numAffected":0,"numAtRisk":180}],"term":"Rash maculo-papular"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"24.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":176},{"groupId":"EG001","numAffected":0,"numAtRisk":180}],"term":"Deep vein thrombosis"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"24.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":176},{"groupId":"EG001","numAffected":0,"numAtRisk":180}],"term":"Lymphoedema"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"24.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":176},{"groupId":"EG001","numAffected":1,"numAtRisk":180}],"term":"Peripheral arterial occlusive disease"}],"timeFrame":"Other (Not including Serious) Adverse Events (AEs) and Serious Adverse Events (SAEs) are collected from first dose to 28 days post last dose (Average of 55.71 months and a maximum up to 95.2 months). Participants were assessed for All-cause mortality from their date of randomization to study completion (Up to approximately 100 months)."}