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22.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":205,"numEvents":1},{"groupId":"EG001","numAffected":0,"numAtRisk":91,"numEvents":0}],"term":"Aortic aneurysm"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA 22.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":205,"numEvents":0},{"groupId":"EG001","numAffected":1,"numAtRisk":91,"numEvents":1}],"term":"Embolism"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA 22.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":205,"numEvents":1},{"groupId":"EG001","numAffected":0,"numAtRisk":91,"numEvents":0}],"term":"Pelvic venous thrombosis"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA 22.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":205,"numEvents":0},{"groupId":"EG001","numAffected":1,"numAtRisk":91,"numEvents":1}],"term":"Phlebitis"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA 22.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":205,"numEvents":0},{"groupId":"EG001","numAffected":1,"numAtRisk":91,"numEvents":1}],"term":"Venous thrombosis"}],"timeFrame":"Adverse events and serious adverse events were collected throughout the study until study completion (up to a maximum of 30 months). 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