{"description":"Treatment-emergent adverse events, defined as adverse events that started or worsened during the on-treatment period (either Randomized or Cross-over Period), have been reported for the Safety Set, which included participants who received at least one dose of drug. 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Cycle 6 crossed over to ruxolitinib treatment.","id":"EG002","otherNumAffected":62,"otherNumAtRisk":70,"seriousNumAffected":27,"seriousNumAtRisk":70,"title":"Ruxolitinib Cross-Over Period"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA (25.1)","stats":[{"groupId":"EG000","numAffected":56,"numAtRisk":165},{"groupId":"EG001","numAffected":25,"numAtRisk":158},{"groupId":"EG002","numAffected":15,"numAtRisk":70}],"term":"Anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA (25.1)","stats":[{"groupId":"EG000","numAffected":10,"numAtRisk":165},{"groupId":"EG001","numAffected":2,"numAtRisk":158},{"groupId":"EG002","numAffected":1,"numAtRisk":70}],"term":"Leukopenia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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