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DARA was administered intravenously (IV) at a starting dose of 16 mg/kg.","id":"EG001","otherNumAffected":112,"otherNumAtRisk":112,"seriousNumAffected":69,"seriousNumAtRisk":112,"title":"Cohort B"},{"deathsNumAffected":8,"deathsNumAtRisk":18,"description":"(Pomalidomide + Daratumumab + low dose Dexamethasone) in Japanese participants with 1 or 2 prior lines of therapy with the most recent line of therapy containing lenalidomide. The starting dose level of POM was 4 mg. The starting dose level of Dex was 40 mg/day (≤75 years old) or 20 mg/day (\\> 75 years old). DARA was administered intravenously (IV) at a starting dose of 16 mg/kg.","id":"EG002","otherNumAffected":18,"otherNumAtRisk":18,"seriousNumAffected":11,"seriousNumAtRisk":18,"title":"Cohort C"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 28.0","stats":[{"groupId":"EG000","numAffected":21,"numAtRisk":56},{"groupId":"EG001","numAffected":33,"numAtRisk":112},{"groupId":"EG002","numAffected":5,"numAtRisk":18}],"term":"Anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 28.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":56},{"groupId":"EG001","numAffected":1,"numAtRisk":112},{"groupId":"EG002","numAffected":1,"numAtRisk":18}],"term":"Febrile neutropenia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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SAEs and Other AEs were assessed from first dose through 30 days following last dose of study treatment (up to approximately 120 months)."}