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(23.0)","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":49,"numEvents":0},{"groupId":"EG001","numAffected":1,"numAtRisk":41,"numEvents":1},{"groupId":"EG002","numAffected":0,"numAtRisk":91,"numEvents":0}],"term":"Disease Complication"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Injury, poisoning and procedural complications","sourceVocabulary":"MedDRA (23.0)","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":49,"numEvents":0},{"groupId":"EG001","numAffected":0,"numAtRisk":41,"numEvents":0},{"groupId":"EG002","numAffected":1,"numAtRisk":91,"numEvents":1}],"term":"Femur Fracture"}],"timeFrame":"Adverse events (AE) were collected from the date of signing the informed consent form up to 47 days after last dose of the study drug, up 36 months."}