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(23.0)","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":232},{"groupId":"EG001","numAffected":0,"numAtRisk":113},{"groupId":"EG002","numAffected":1,"numAtRisk":80}],"term":"Musculoskeletal chest pain"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","sourceVocabulary":"MedDRA (23.0)","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":232},{"groupId":"EG001","numAffected":0,"numAtRisk":113},{"groupId":"EG002","numAffected":1,"numAtRisk":80}],"term":"Arterial occlusive disease"}],"timeFrame":"Adverse events were reported from date of first dose of study drug until 28 days after last dose of study drug, approximately 3.5 years."}