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(26.1)","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":189},{"groupId":"EG001","numAffected":1,"numAtRisk":175},{"groupId":"EG002","numAffected":0,"numAtRisk":100},{"groupId":"EG003","numAtRisk":0},{"groupId":"EG004","numAtRisk":0},{"groupId":"EG005","numAtRisk":0}],"term":"Peripheral artery occlusion"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA (26.1)","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":189},{"groupId":"EG001","numAffected":2,"numAtRisk":175},{"groupId":"EG002","numAffected":0,"numAtRisk":100},{"groupId":"EG003","numAtRisk":0},{"groupId":"EG004","numAtRisk":0},{"groupId":"EG005","numAtRisk":0}],"term":"Superior vena cava syndrome"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA (26.1)","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":189},{"groupId":"EG001","numAffected":1,"numAtRisk":175},{"groupId":"EG002","numAffected":0,"numAtRisk":100},{"groupId":"EG003","numAtRisk":0},{"groupId":"EG004","numAtRisk":0},{"groupId":"EG005","numAtRisk":0}],"term":"Venous thrombosis limb"}],"timeFrame":"All-cause mortality: from randomization up to approx. 120 months, including post-treatment survival follow-up period. Serious and Other Adverse Events (AEs): from first dose of study treatment until 30 days after last dose (or start of crossover treatment), up to approx. 120 months. For participants who crossed over, AEs were also collected from start of crossover treatment to 30 days post-crossover treatment (extension-treatment period), up to approx. 108 months."}