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25.1","stats":[{"groupId":"EG000","numAffected":2,"numAtRisk":337,"numEvents":2},{"groupId":"EG001","numAffected":1,"numAtRisk":343,"numEvents":1}],"term":"Hyperuricaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Metabolism and nutrition disorders","sourceVocabulary":"MedDRA 25.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":337,"numEvents":0},{"groupId":"EG001","numAffected":1,"numAtRisk":343,"numEvents":1}],"term":"Hyponatraemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Musculoskeletal and connective tissue disorders","sourceVocabulary":"MedDRA 25.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":337,"numEvents":1},{"groupId":"EG001","numAffected":0,"numAtRisk":343,"numEvents":0}],"term":"Bone hypertrophy"}],"timeFrame":"Adverse events with onset date on or after the date of first dose up to and including 28 days following discontinuation of study treatment and before starting subsequent cancer therapy, up to approximately 3 years. All-Cause Mortality assessed up to approximately 7 years."}