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disorders","sourceVocabulary":"25.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":182},{"groupId":"EG001","numAffected":1,"numAtRisk":179}],"term":"Haematoma"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"25.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":182},{"groupId":"EG001","numAffected":0,"numAtRisk":179}],"term":"Hypertensive urgency"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"25.1","stats":[{"groupId":"EG000","numAffected":3,"numAtRisk":182},{"groupId":"EG001","numAffected":0,"numAtRisk":179}],"term":"Hypotension"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"25.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":182},{"groupId":"EG001","numAffected":0,"numAtRisk":179}],"term":"Orthostatic hypotension"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"25.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":182},{"groupId":"EG001","numAffected":0,"numAtRisk":179}],"term":"Peripheral ischaemia"}],"timeFrame":"All-cause mortality was assessed from a participants first dose to primary completion (up to approximately 221 weeks). SAEs and Other AEs were assessed from first dose to 42 days post last dose (up to approximately an average of 72 weeks and a maximum of 208 weeks)."}