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(14.1)","stats":[{"groupId":"EG000","numAffected":2,"numAtRisk":147},{"groupId":"EG001","numAffected":2,"numAtRisk":134},{"groupId":"EG002","numAffected":0,"numAtRisk":117}],"term":"Pleural Effusion"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Respiratory, thoracic and mediastinal disorders","sourceVocabulary":"MedDRA (14.1)","stats":[{"groupId":"EG000","numAffected":3,"numAtRisk":147},{"groupId":"EG001","numAffected":1,"numAtRisk":134},{"groupId":"EG002","numAffected":0,"numAtRisk":117}],"term":"Pulmonary Embolism"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA (14.1)","stats":[{"groupId":"EG000","numAffected":2,"numAtRisk":147},{"groupId":"EG001","numAffected":3,"numAtRisk":134},{"groupId":"EG002","numAffected":0,"numAtRisk":117}],"term":"Deep Vein Thrombosis"}],"timeFrame":"Study drug initiation through 30 days after the last dose of study drug or EOS, whichever is later; Up to 764 days."}