{"description":"SAEs and other AEs: The safety analysis set included all participants who received at least 1 dose of any study treatment (partial or complete). All-cause mortality: all randomized analysis set included all participants who were randomized in the study .","eventGroups":[{"deathsNumAffected":59,"deathsNumAtRisk":198,"description":"Participants with multiple myeloma received a single dose of bortezomib 1.3 milligrams per square meter (mg/m\\^2) as subcutaneous (SC) injection twice weekly on Days 1, 4, 8 and 11 of Cycles 1 to 8. Lenalidomide 25 milligrams (mg) capsule were administered orally once daily from Day 1 to Day 14 of Cycles 1 to 8. Starting from Cycle 9, Lenalidomide capsules were administered orally once daily from Day 1 to Day 21 until disease progression or unacceptable toxicity during treatment phase. Dexamethasone 20 mg was administered as a single dose oral tablet on Days 1, 2, 4, 5, 8, 9, 11, 12 during Cycle 1 to 8. Participants aged greater than \\[\\>\\]75 years or underweight (body mass index \\[BMI\\] less than \\[\\<\\]18.5 kilograms per meters \\[kg/m\\^2\\]) were administered with Dexamethasone 20 mg oral tablets on Days 1, 4, 8, and 11 of each cycle. Starting from Cycle 9, Dexamethasone 40 mg was administered as a single tablet orally on Days 1, 8, 15, and 22 of each cycle until disease progression or unacceptable toxicity during treatment phase. Cycles 1 to 8 were 21 days each while Cycles 9 and beyond were 28 days each.","id":"EG000","otherNumAffected":191,"otherNumAtRisk":195,"seriousNumAffected":131,"seriousNumAtRisk":195,"title":"Arm A: Bortezomib-lenalidomide-dexamethasone (VRd)"},{"deathsNumAffected":51,"deathsNumAtRisk":197,"description":"Participants with multiple myeloma received a single dose of daratumumab 1800 mg as SC injection once every week in Cycles 1-2, every 3 weeks in Cycles 3-8, and every 4 weeks in Cycle 9 and beyond until disease progression or unacceptable toxicity. Bortezomib 1.3 mg/m\\^2 SC injection was administered twice weekly on Days 1, 4, 8 and 11 of Cycles 1 to 8. Lenalidomide 25 mg capsule was administered orally once daily from Day 1 to Day 14 of Cycles 1 to 8. Starting from Cycle 9, Lenalidomide capsules were administered orally once daily from Day 1 to Day 21 of each cycle until disease progression or unacceptable toxicity during treatment phase. Dexamethasone 20 mg was administered as a single oral tablet on Days 1, 2, 4, 5, 8, 9, 11, 12 of Cycle 1 to 8. Participants aged \\>75 years or underweight (BMI \\<18.5 kg/m\\^2) were administered with Dexamethasone 20 mg oral tablets on Days 1, 4, 8, and 11 of each cycle. Starting from Cycle 9, Dexamethasone 40 mg was administered as a single tablet orally on Days 1, 8, 15, and 22 of each cycle until disease progression or unacceptable toxicity during treatment phase. Cycles 1 to 8 were 21 days each while Cycles 9 and beyond were 28 days each.","id":"EG001","otherNumAffected":196,"otherNumAtRisk":197,"seriousNumAffected":142,"seriousNumAtRisk":197,"title":"Arm B: Daratumumab-bortezomib-lenalidomide-dexamethasone (D-VRd)"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA Version 23.0","stats":[{"groupId":"EG000","numAffected":62,"numAtRisk":195},{"groupId":"EG001","numAffected":71,"numAtRisk":197}],"term":"Anaemia"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA Version 23.0","stats":[{"groupId":"EG000","numAffected":19,"numAtRisk":195},{"groupId":"EG001","numAffected":28,"numAtRisk":197}],"term":"Leukopenia"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA Version 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Fibrillation"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Ear and labyrinth disorders","sourceVocabulary":"MedDRA Version 23.0","stats":[{"groupId":"EG000","numAffected":4,"numAtRisk":195},{"groupId":"EG001","numAffected":12,"numAtRisk":197}],"term":"Tinnitus"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Ear and labyrinth disorders","sourceVocabulary":"MedDRA Version 23.0","stats":[{"groupId":"EG000","numAffected":13,"numAtRisk":195},{"groupId":"EG001","numAffected":16,"numAtRisk":197}],"term":"Vertigo"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Eye disorders","sourceVocabulary":"MedDRA Version 23.0","stats":[{"groupId":"EG000","numAffected":50,"numAtRisk":195},{"groupId":"EG001","numAffected":53,"numAtRisk":197}],"term":"Cataract"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Eye disorders","sourceVocabulary":"MedDRA Version 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