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(24.1)","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":554},{"groupId":"EG001","numAffected":1,"numAtRisk":548},{"groupId":"EG002","numAtRisk":0},{"groupId":"EG003","numAtRisk":0}],"term":"Haematoma"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA (24.1)","stats":[{"groupId":"EG000","numAffected":7,"numAtRisk":554},{"groupId":"EG001","numAffected":6,"numAtRisk":548},{"groupId":"EG002","numAtRisk":0},{"groupId":"EG003","numAtRisk":0}],"term":"Hypertension"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA (24.1)","stats":[{"groupId":"EG000","numAffected":2,"numAtRisk":554},{"groupId":"EG001","numAffected":1,"numAtRisk":548},{"groupId":"EG002","numAtRisk":0},{"groupId":"EG003","numAtRisk":0}],"term":"Hypertensive crisis"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA (24.1)","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":554},{"groupId":"EG001","numAffected":1,"numAtRisk":548},{"groupId":"EG002","numAtRisk":0},{"groupId":"EG003","numAtRisk":0}],"term":"Hypotension"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA (24.1)","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":554},{"groupId":"EG001","numAffected":1,"numAtRisk":548},{"groupId":"EG002","numAtRisk":0},{"groupId":"EG003","numAtRisk":0}],"term":"Orthostatic hypotension"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA (24.1)","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":554},{"groupId":"EG001","numAffected":1,"numAtRisk":548},{"groupId":"EG002","numAtRisk":0},{"groupId":"EG003","numAtRisk":0}],"term":"Thrombosis"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA (24.1)","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":554},{"groupId":"EG001","numAffected":1,"numAtRisk":548},{"groupId":"EG002","numAtRisk":0},{"groupId":"EG003","numAtRisk":0}],"term":"Vena cava thrombosis"}],"timeFrame":"Adverse Events (AEs) were collected from first dose of study medication until the last dose plus 28 days post-treat follow-up, assessed up to approximately 129 months. Deaths were recorded from study start date until end of survival follow-up phase (end of study), assessed up to approximately 152 months."}