{"description":"All treated population included all participants who received at least one dose of study treatment.","eventGroups":[{"deathsNumAffected":3,"deathsNumAtRisk":12,"description":"Participants with Relapsed or Refractory Multiple Myeloma (RRMM) received belantamab mafodotin as 1.9 milligram (mg)/kilogram (kg) dose on Day 1 of every alternate 28-day cycles (C1, C3, C5, C7 and so on) as a 30-60 minute infusion. Along with belantamab mafodotin, Lenalidomide (Len) was administered as 25 mg or 10 mg per oral (PO) on Days 1-21 of each 28-day cycle with 40 mg Dexamethasone (Dex) weekly PO/ intravenously (IV) on Days 1, 8, 15 and 22 of each cycle.","id":"EG000","otherNumAffected":12,"otherNumAtRisk":12,"seriousNumAffected":6,"seriousNumAtRisk":12,"title":"Main Study Phase: Belantamab Mafodotin 1.9mg/kg STRETCH + Len/Dex"},{"deathsNumAffected":2,"deathsNumAtRisk":4,"description":"Participants with RRMM received belantamab mafodotin as SINGLE full dose of 1.9 mg/kg on Day 1 of every 28-day cycle as a 30-60 minute infusion. Along with belantamab mafodotin, Lenalidomide was administered as 25 mg or 10 mg PO on Days 1-21 of each 28-day cycle with 40 mg Dexamethasone weekly PO/ IV on Days 1, 8, 15 and 22 of each cycle.","id":"EG001","otherNumAffected":4,"otherNumAtRisk":4,"seriousNumAffected":2,"seriousNumAtRisk":4,"title":"Main Study Phase: Belantamab Mafodotin 1.9mg/kg SINGLE + Len/Dex"},{"deathsNumAffected":6,"deathsNumAtRisk":13,"description":"Participants with RRMM received belantamab mafodotin as two equal divided doses of a total 2.5mg/kg dose as a 1.25 mg/kg dose on Day 1 and a 1.25 mg/kg dose on Day 8 of each 28-day cycle as a 30-60 minute infusion. Along with belantamab mafodotin, Lenalidomide was administered as 25 mg or 10 mg PO on Days 1-21 of each 28-day cycle with 40 mg Dexamethasone weekly PO/ IV on Days 1, 8, 15 and 22 of each cycle.","id":"EG002","otherNumAffected":13,"otherNumAtRisk":13,"seriousNumAffected":6,"seriousNumAtRisk":13,"title":"Main Study Phase: Belantamab Mafodotin 2.5mg/kg SPLIT + Len/Dex"},{"deathsNumAffected":8,"deathsNumAtRisk":16,"description":"Participants with RRMM received belantamab mafodotin as SINGLE full dose of 2.5 mg/kg on Day 1 of every 28-day cycle as a 30-60 minute infusion. Along with belantamab mafodotin, Lenalidomide was administered as 25 mg or 10 mg PO on Days 1-21 of each 28-day cycle with 40 mg Dexamethasone weekly PO/ IV on Days 1, 8, 15 and 22 of each cycle.","id":"EG003","otherNumAffected":16,"otherNumAtRisk":16,"seriousNumAffected":10,"seriousNumAtRisk":16,"title":"Main Study Phase: Belantamab Mafodotin 2.5mg/kg SINGLE + Len/Dex"},{"deathsNumAffected":4,"deathsNumAtRisk":12,"description":"Participants with RRMM received belantamab mafodotin as 1.9 mg/kg dose on Day 1 of every alternate 21-day cycle (C1, C3, C5, C7, and so on) as a 30-60 minute infusion. Along with belantamab mafodotin, Bortezomib (Bor) was administered as 1.3 milligrams per square meters (mg/m\\^2) subcutaneously (SC) /IV on Days 1, 4, 8, and 11 with 20 mg Dexamethasone (Dex) PO/IV on Days 1, 2, 4, 5, 8, 9, 11, and 12 of every 21-day cycle up to 8 cycles.","id":"EG004","otherNumAffected":12,"otherNumAtRisk":12,"seriousNumAffected":8,"seriousNumAtRisk":12,"title":"Main Study Phase: Belantamab Mafodotin 1.9 mg/kg STRETCH + Bor/Dex"},{"deathsNumAffected":2,"deathsNumAtRisk":12,"description":"Participants with RRMM received belantamab mafodotin as SINGLE full dose of 1.9 mg/kg on Day 1 of every 21-day cycle as a 30-60 minute infusion. Along with belantamab mafodotin, Bortezomib was administered as 1.3 mg/m\\^2 SC /IV on Days 1, 4, 8, and 11 with 20 mg Dexamethasone PO/IV on Days 1, 2, 4, 5, 8, 9, 11, and 12 of every 21-day cycle up to 8 cycles.","id":"EG005","otherNumAffected":12,"otherNumAtRisk":12,"seriousNumAffected":8,"seriousNumAtRisk":12,"title":"Main Study Phase: Belantamab Mafodotin 1.9 mg/kg SINGLE + Bor/Dex"},{"deathsNumAffected":4,"deathsNumAtRisk":12,"description":"Participants with RRMM received belantamab mafodotin as 2.5 mg/kg dose on cycle 1 day 1 (C1D1) followed by 1.9 mg/kg step-down dose on Day 1 of every alternate 21-day cycles C3 onwards (C3, C5, C7, and so on) as a 30-60 minute infusion. Along with belantamab mafodotin, Bortezomib was administered as 1.3 mg/m\\^2 SC /IV on Days 1, 4, 8, and 11 with 20 mg Dexamethasone PO/IV on Days 1, 2, 4, 5, 8, 9, 11, and 12 of every 21-day cycle up to 8 cycles.","id":"EG006","otherNumAffected":12,"otherNumAtRisk":12,"seriousNumAffected":6,"seriousNumAtRisk":12,"title":"Main Study Phase: Belantamab Mafodotin 2.5 mg/kg Step-Down STRETCH+ Bor/Dex"},{"deathsNumAffected":5,"deathsNumAtRisk":12,"description":"Participants with RRMM received belantamab mafodotin as 2.5 mg/kg dose on Day 1 of every alternate 21-day cycles (C1, C3, C5, C7, and so on) as a 30-60 minute infusion. Along with belantamab mafodotin, Bortezomib was administered as 1.3 mg/m\\^2 SC /IV on Days 1, 4, 8, and 11 with 20 mg Dexamethasone PO/IV on Days 1, 2, 4, 5, 8, 9, 11, and 12 of every 21-day cycle up to 8 cycles.","id":"EG007","otherNumAffected":12,"otherNumAtRisk":12,"seriousNumAffected":6,"seriousNumAtRisk":12,"title":"Main Study Phase: Belantamab Mafodotin 2.5 mg/kg STRETCH + Bor/Dex"},{"deathsNumAffected":5,"deathsNumAtRisk":13,"description":"Participants with RRMM received belantamab mafodotin as two equal divided doses of a total 2.5mg/kg dose as a 1.25 mg/kg on Day 1 and 1.25 mg/kg dose on Day 8 of every 21-day cycle as a 30-60 minute infusion. Along with belantamab mafodotin, Bortezomib was administered as 1.3 mg/m\\^2 SC /IV on Days 1, 4, 8, and 11 with 20 mg Dexamethasone PO/IV on Days 1, 2, 4, 5, 8, 9, 11, and 12 of every 21-day cycle up to 8 cycles.","id":"EG008","otherNumAffected":13,"otherNumAtRisk":13,"seriousNumAffected":7,"seriousNumAtRisk":13,"title":"Main Study Phase: Belantamab Mafodotin 2.5 mg/kg SPLIT + Bor/Dex"},{"deathsNumAffected":8,"deathsNumAtRisk":18,"description":"Participants with RRMM received belantamab mafodotin as SINGLE full dose of 2.5 mg/kg on Day 1 of every 21-day cycle as a 30-60 minute infusion. Along with belantamab mafodotin, Bortezomib was administered as 1.3 mg/m\\^2 SC /IV on Days 1, 4, 8, and 11 with 20 mg Dexamethasone PO/IV on Days 1, 2, 4, 5, 8, 9, 11, and 12 of every 21-day cycle up to 8 cycles.","id":"EG009","otherNumAffected":18,"otherNumAtRisk":18,"seriousNumAffected":13,"seriousNumAtRisk":18,"title":"Main Study Phase: Belantamab Mafodotin 2.5 mg/kg SINGLE + Bor/Dex"},{"deathsNumAffected":6,"deathsNumAtRisk":12,"description":"Participants with RRMM received belantamab mafodotin as two equal divided doses of a total 3.4 mg/kg dose as a 1.7 mg/kg dose on Day 1 and 1.7 mg/kg on Day 8 of every 21-day cycle as a 30-60 minute infusion. Along with belantamab mafodotin, Bortezomib was administered as 1.3 mg/m\\^2 SC /IV on Days 1, 4, 8, and 11 with 20 mg Dexamethasone PO/IV on Days 1, 2, 4, 5, 8, 9, 11, and 12 of every 21-day cycle up to 8 cycles.","id":"EG010","otherNumAffected":12,"otherNumAtRisk":12,"seriousNumAffected":6,"seriousNumAtRisk":12,"title":"Main Study Phase: Belantamab Mafodotin 3.4 mg/kg SPLIT + Bor/Dex"},{"deathsNumAffected":4,"deathsNumAtRisk":16,"description":"Participants with RRMM received belantamab mafodotin as SINGLE full dose of 3.4 mg/kg on Day 1 of every 21-day cycle as a 30-60 minute infusion. Along with belantamab mafodotin, Bortezomib was administered as 1.3 mg/m\\^2 SC /IV on Days 1, 4, 8, and 11 with 20 mg Dexamethasone PO/IV on Days 1, 2, 4, 5, 8, 9, 11, and 12 of every 21-day cycle up to 8 cycles.","id":"EG011","otherNumAffected":16,"otherNumAtRisk":16,"seriousNumAffected":9,"seriousNumAtRisk":16,"title":"Main Study Phase: Belantamab Mafodotin 3.4 mg/kg SINGLE + Bor/Dex"},{"deathsNumAffected":0,"deathsNumAtRisk":3,"description":"Participants with Relapsed or Refractory Multiple Myeloma (RRMM) received belantamab mafodotin as 1.9 milligram (mg)/kilogram (kg) dose on Day 1 of every alternate 28-day cycles (C1, C3, C5, C7 and so on) as a 30-60 minute infusion. Along with belantamab mafodotin, Lenalidomide (Len) was administered as 25 mg or 10 mg per oral (PO) on Days 1-21 of each 28-day cycle with 40 mg Dexamethasone (Dex) weekly PO/ intravenously (IV) on Days 1, 8, 15 and 22 of each cycle until PD, death, intolerable toxicity, or consent withdrawn.","id":"EG012","otherNumAffected":0,"otherNumAtRisk":3,"seriousNumAffected":1,"seriousNumAtRisk":3,"title":"PACT Phase: Belantamab Mafodotin 1.9mg/kg STRETCH + Len/Dex"},{"deathsNumAffected":0,"deathsNumAtRisk":1,"description":"Participants with RRMM received belantamab mafodotin as SINGLE full dose of 1.9 mg/kg on Day 1 of every 28-day cycle as a 30-60 minute infusion. Along with belantamab mafodotin, Lenalidomide was administered as 25 mg or 10 mg PO on Days 1-21 of each 28-day cycle with 40 mg Dexamethasone weekly PO/ IV on Days 1, 8, 15 and 22 of each cycle until PD, death, intolerable toxicity, or consent withdrawn.","id":"EG013","otherNumAffected":0,"otherNumAtRisk":1,"seriousNumAffected":0,"seriousNumAtRisk":1,"title":"PACT Phase: Belantamab Mafodotin 1.9mg/kg SINGLE + Len/Dex"},{"deathsNumAffected":0,"deathsNumAtRisk":2,"description":"Participants with RRMM received belantamab mafodotin as two equal divided doses of a total 2.5mg/kg dose as a 1.25 mg/kg dose on Day 1 and a 1.25 mg/kg dose on Day 8 of each 28-day cycle as a 30-60 minute infusion. Along with belantamab mafodotin, Lenalidomide was administered as 25 mg or 10 mg PO on Days 1-21 of each 28-day cycle with 40 mg Dexamethasone weekly PO/ IV on Days 1, 8, 15 and 22 of each cycle until PD, death, intolerable toxicity, or consent withdrawn.","id":"EG014","otherNumAffected":0,"otherNumAtRisk":2,"seriousNumAffected":0,"seriousNumAtRisk":2,"title":"PACT Phase: Belantamab Mafodotin 2.5mg/kg SPLIT + Len/Dex"},{"deathsNumAffected":0,"deathsNumAtRisk":4,"description":"Participants with RRMM received belantamab mafodotin as SINGLE full dose of 2.5 mg/kg on Day 1 of every 28-day cycle as a 30-60 minute infusion. Along with belantamab mafodotin, Lenalidomide was administered as 25 mg or 10 mg PO on Days 1-21 of each 28-day cycle with 40 mg Dexamethasone weekly PO/ IV on Days 1, 8, 15 and 22 of each cycle until PD, death, intolerable toxicity, or consent withdrawn.","id":"EG015","otherNumAffected":0,"otherNumAtRisk":4,"seriousNumAffected":2,"seriousNumAtRisk":4,"title":"PACT Phase: Belantamab Mafodotin 2.5mg/kg SINGLE + Len/Dex"},{"deathsNumAffected":0,"deathsNumAtRisk":2,"description":"Participants with RRMM received belantamab mafodotin as 1.9 mg/kg dose on Day 1 of every alternate 21-day cycle (C1, C3, C5, C7, and so on) as a 30-60 minute infusion. Along with belantamab mafodotin, Bortezomib (Bor) was administered as 1.3 milligrams per square meters (mg/m\\^2) subcutaneously (SC) /IV on Days 1, 4, 8, and 11 with 20 mg Dexamethasone (Dex) PO/IV on Days 1, 2, 4, 5, 8, 9, 11, and 12 of every 21-day cycle up to 8 cycles followed by belantamab mafodotin monotherapy as 1.9 mg/kg dose until PD, death, intolerable toxicity, or consent withdrawn.","id":"EG016","otherNumAffected":0,"otherNumAtRisk":2,"seriousNumAffected":1,"seriousNumAtRisk":2,"title":"PACT Phase: Belantamab Mafodotin 1.9 mg/kg STRETCH + Bor/Dex"},{"deathsNumAffected":0,"deathsNumAtRisk":4,"description":"Participants with RRMM received belantamab mafodotin as SINGLE full dose of 1.9 mg/kg on Day 1 of every 21-day cycle as a 30-60 minute infusion. Along with belantamab mafodotin, Bortezomib was administered as 1.3 mg/m\\^2 SC /IV on Days 1, 4, 8, and 11 with 20 mg Dexamethasone PO/IV on Days 1, 2, 4, 5, 8, 9, 11, and 12 of every 21-day cycle up to 8 cycles followed by belantamab mafodotin monotherapy as 1.9 mg/kg dose until PD, death, intolerable toxicity, or consent withdrawn.","id":"EG017","otherNumAffected":0,"otherNumAtRisk":4,"seriousNumAffected":1,"seriousNumAtRisk":4,"title":"PACT Phase: Belantamab Mafodotin 1.9 mg/kg SINGLE + Bor/Dex"},{"deathsNumAffected":0,"deathsNumAtRisk":4,"description":"Participants with RRMM received belantamab mafodotin as 2.5 mg/kg dose on cycle 1 day 1 (C1D1) followed by 1.9 mg/kg step-down dose on Day 1 of every alternate 21-day cycles C3 onwards (C3, C5, C7, and so on) as a 30-60 minute infusion. Along with belantamab mafodotin, Bortezomib was administered as 1.3 mg/m\\^2 SC /IV on Days 1, 4, 8, and 11 with 20 mg Dexamethasone PO/IV on Days 1, 2, 4, 5, 8, 9, 11, and 12 of every 21-day cycle up to 8 cycles followed by belantamab mafodotin monotherapy as 2.5 mg/kg dose until PD, death, intolerable toxicity, or consent withdrawn.","id":"EG018","otherNumAffected":0,"otherNumAtRisk":4,"seriousNumAffected":1,"seriousNumAtRisk":4,"title":"PACT Phase: Belantamab Mafodotin 2.5 mg/kg Step-Down STRETCH+ Bor/Dex"},{"deathsNumAffected":0,"deathsNumAtRisk":2,"description":"Participants with RRMM received belantamab mafodotin as two equal divided doses of a total 2.5mg/kg dose as a 1.25 mg/kg on Day 1 and 1.25 mg/kg dose on Day 8 of every 21-day cycle as a 30-60 minute infusion. Along with belantamab mafodotin, Bortezomib was administered as 1.3 mg/m\\^2 SC /IV on Days 1, 4, 8, and 11 with 20 mg Dexamethasone PO/IV on Days 1, 2, 4, 5, 8, 9, 11, and 12 of every 21-day cycle up to 8 cycles followed by belantamab mafodotin monotherapy as 2.5 mg/kg dose until PD, death, intolerable toxicity, or consent withdrawn.","id":"EG019","otherNumAffected":0,"otherNumAtRisk":2,"seriousNumAffected":0,"seriousNumAtRisk":2,"title":"PACT Phase: Belantamab Mafodotin 2.5 mg/kg SPLIT + Bor/Dex"},{"deathsNumAffected":0,"deathsNumAtRisk":2,"description":"Participants with RRMM received belantamab mafodotin as SINGLE full dose of 2.5 mg/kg on Day 1 of every 21-day cycle as a 30-60 minute infusion. Along with belantamab mafodotin, Bortezomib was administered as 1.3 mg/m\\^2 SC /IV on Days 1, 4, 8, and 11 with 20 mg Dexamethasone PO/IV on Days 1, 2, 4, 5, 8, 9, 11, and 12 of every 21-day cycle up to 8 cycles followed by belantamab mafodotin monotherapy as 2.5 mg/kg dose until PD, death, intolerable toxicity, or consent withdrawn.","id":"EG020","otherNumAffected":0,"otherNumAtRisk":2,"seriousNumAffected":0,"seriousNumAtRisk":2,"title":"PACT Phase: Belantamab Mafodotin 2.5 mg/kg SINGLE + Bor/Dex"},{"deathsNumAffected":0,"deathsNumAtRisk":1,"description":"Participants with RRMM received belantamab mafodotin as two equal divided doses of a total 3.4 mg/kg dose as a 1.7 mg/kg dose on Day 1 and 1.7 mg/kg on Day 8 of every 21-day cycle as a 30-60 minute infusion. Along with belantamab mafodotin, Bortezomib was administered as 1.3 mg/m\\^2 SC /IV on Days 1, 4, 8, and 11 with 20 mg Dexamethasone PO/IV on Days 1, 2, 4, 5, 8, 9, 11, and 12 of every 21-day cycle up to 8 cycles followed by belantamab mafodotin monotherapy as 3.4 mg/kg dose until PD, death, intolerable toxicity, or consent withdrawn.","id":"EG021","otherNumAffected":0,"otherNumAtRisk":1,"seriousNumAffected":0,"seriousNumAtRisk":1,"title":"PACT Phase: Belantamab Mafodotin 3.4 mg/kg SPLIT + Bor/Dex"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA v 25.1","stats":[{"groupId":"EG000","numAffected":2,"numAtRisk":12,"numEvents":2},{"groupId":"EG001","numAffected":0,"numAtRisk":4,"numEvents":0},{"groupId":"EG002","numAffected":4,"numAtRisk":13,"numEvents":5},{"groupId":"EG003","numAffected":5,"numAtRisk":16,"numEvents":5},{"groupId":"EG004","numAffected":1,"numAtRisk":12,"numEvents":1},{"groupId":"EG005","numAffected":3,"numAtRisk":12,"numEvents":6},{"groupId":"EG006","numAffected":2,"numAtRisk":12,"numEvents":2},{"groupId":"EG007","numAffected":3,"numAtRisk":12,"numEvents":3},{"groupId":"EG008","numAffected":3,"numAtRisk":13,"numEvents":3},{"groupId":"EG009","numAffected":4,"numAtRisk":18,"numEvents":5},{"groupId":"EG010","numAffected":2,"numAtRisk":12,"numEvents":2},{"groupId":"EG011","numAffected":2,"numAtRisk":16,"numEvents":2},{"groupId":"EG012","numAffected":0,"numAtRisk":3},{"groupId":"EG013","numAffected":0,"numAtRisk":1},{"groupId":"EG014","numAffected":0,"numAtRisk":2},{"groupId":"EG015","numAffected":0,"numAtRisk":4},{"groupId":"EG016","numAffected":0,"numAtRisk":2},{"groupId":"EG017","numAffected":0,"numAtRisk":4},{"groupId":"EG018","numAffected":0,"numAtRisk":4},{"groupId":"EG019","numAffected":0,"numAtRisk":2},{"groupId":"EG020","numAffected":0,"numAtRisk":2},{"groupId":"EG021","numAffected":0,"numAtRisk":1}],"term":"Anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA v 25.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":12,"numEvents":0},{"groupId":"EG001","numAffected":0,"numAtRisk":4,"numEvents":0},{"groupId":"EG002","numAffected":0,"numAtRisk":13,"numEvents":0},{"groupId":"EG003","numAffected":0,"numAtRisk":16,"numEvents":0},{"groupId":"EG004","numAffected":0,"numAtRisk":12,"numEvents":0},{"groupId":"EG005","numAffected":1,"numAtRisk":12,"numEvents":1},{"groupId":"EG006","numAffected":0,"numAtRisk":12,"numEvents":0},{"groupId":"EG007","numAffected":1,"numAtRisk":12,"numEvents":1},{"groupId":"EG008","numAffected":0,"numAtRisk":13,"numEvents":0},{"groupId":"EG009","numAffected":0,"numAtRisk":18,"numEvents":0},{"groupId":"EG010","numAffected":0,"numAtRisk":12,"numEvents":0},{"groupId":"EG011","numAffected":0,"numAtRisk":16,"numEvents":0},{"groupId":"EG012","numAffected":0,"numAtRisk":3},{"groupId":"EG013","numAffected":0,"numAtRisk":1},{"groupId":"EG014","numAffected":0,"numAtRisk":2},{"groupId":"EG015","numAffected":0,"numAtRisk":4},{"groupId":"EG016","numAffected":0,"numAtRisk":2},{"groupId":"EG017","numAffected":0,"numAtRisk":4},{"groupId":"EG018","numAffected":0,"numAtRisk":4},{"groupId":"EG019","numAffected":0,"numAtRisk":2},{"groupId":"EG020","numAffected":0,"numAtRisk":2},{"groupId":"EG021","numAffected":0,"numAtRisk":1}],"term":"Febrile neutropenia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA v 25.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":12,"numEvents":0},{"groupId":"EG001","numAffected":0,"numAtRisk":4,"numEvents":0},{"groupId":"EG002","numAffected":0,"numAtRisk":13,"numEvents":0},{"groupId":"EG003","numAffected":0,"numAtRisk":16,"numEvents":0},{"groupId":"EG004","numAffected":0,"numAtRisk":12,"numEvents":0},{"groupId":"EG005","numAffected":0,"numAtRisk":12,"numEvents":0},{"groupId":"EG006","numAffected":0,"numAtRisk":12,"numEvents":0},{"groupId":"EG007","numAffected":1,"numAtRisk":12,"numEvents":1},{"groupId":"EG008","numAffected":0,"numAtRisk":13,"numEvents":0},{"groupId":"EG009","numAffected":0,"numAtRisk":18,"numEvents":0},{"groupId":"EG010","numAffected":0,"numAtRisk":12,"numEvents":0},{"groupId":"EG011","numAffected":0,"numAtRisk":16,"numEvents":0},{"groupId":"EG012","numAffected":0,"numAtRisk":3},{"groupId":"EG013","numAffected":0,"numAtRisk":1},{"groupId":"EG014","numAffected":0,"numAtRisk":2},{"groupId":"EG015","numAffected":0,"numAtRisk":4},{"groupId":"EG016","numAffected":0,"numAtRisk":2},{"groupId":"EG017","numAffected":0,"numAtRisk":4},{"groupId":"EG018","numAffected":0,"numAtRisk":4},{"groupId":"EG019","numAffected":0,"numAtRisk":2},{"groupId":"EG020","numAffected":0,"numAtRisk":2},{"groupId":"EG021","numAffected":0,"numAtRisk":1}],"term":"Iron deficiency anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA v 25.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":12,"numEvents":0},{"groupId":"EG001","numAffected":0,"numAtRisk":4,"numEvents":0},{"groupId":"EG002","numAffected":0,"numAtRisk":13,"numEvents":0},{"groupId":"EG003","numAffected":0,"numAtRisk":16,"numEvents":0},{"groupId":"EG004","numAffected":0,"numAtRisk":12,"numEvents":0},{"groupId":"EG005","numAffected":0,"numAtRisk":12,"numEvents":0},{"groupId":"EG006","numAffected":0,"numAtRisk":12,"numEvents":0},{"groupId":"EG007","numAffected":0,"numAtRisk":12,"numEvents":0},{"groupId":"EG008","numAffected":0,"numAtRisk":13,"numEvents":0},{"groupId":"EG009","numAffected":1,"numAtRisk":18,"numEvents":1},{"groupId":"EG010","numAffected":0,"numAtRisk":12,"numEvents":0},{"groupId":"EG011","numAffected":0,"numAtRisk":16,"numEvents":0},{"groupId":"EG012","numAffected":0,"numAtRisk":3},{"groupId":"EG013","numAffected":0,"numAtRisk":1},{"groupId":"EG014","numAffected":0,"numAtRisk":2},{"groupId":"EG015","numAffected":0,"numAtRisk":4},{"groupId":"EG016","numAffected":0,"numAtRisk":2},{"groupId":"EG017","numAffected":0,"numAtRisk":4},{"groupId":"EG018","numAffected":0,"numAtRisk":4},{"groupId":"EG019","numAffected":0,"numAtRisk":2},{"groupId":"EG020","numAffected":0,"numAtRisk":2},{"groupId":"EG021","numAffected":0,"numAtRisk":1}],"term":"Leukocytosis"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA v 25.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":12,"numEvents":2},{"groupId":"EG001","numAffected":0,"numAtRisk":4,"numEvents":0},{"groupId":"EG002","numAffected":1,"numAtRisk":13,"numEvents":1},{"groupId":"EG003","numAffected":1,"numAtRisk":16,"numEvents":1},{"groupId":"EG004","numAffected":0,"numAtRisk":12,"numEvents":0},{"groupId":"EG005","numAffected":1,"numAtRisk":12,"numEvents":2},{"groupId":"EG006","numAffected":0,"numAtRisk":12,"numEvents":0},{"groupId":"EG007","numAffected":0,"numAtRisk":12,"numEvents":0},{"groupId":"EG008","numAffected":0,"numAtRisk":13,"numEvents":0},{"groupId":"EG009","numAffected":0,"numAtRisk":18,"numEvents":0},{"groupId":"EG010","numAffected":0,"numAtRisk":12,"numEvents":0},{"groupId":"EG011","numAffected":0,"numAtRisk":16,"numEvents":0},{"groupId":"EG012","numAffected":0,"numAtRisk":3},{"groupId":"EG013","numAffected":0,"numAtRisk":1},{"groupId":"EG014","numAffected":0,"numAtRisk":2},{"groupId":"EG015","numAffected":0,"numAtRisk":4},{"groupId":"EG016","numAffected":0,"numAtRisk":2},{"groupId":"EG017","numAffected":0,"numAtRisk":4},{"groupId":"EG018","numAffected":0,"numAtRisk":4},{"groupId":"EG019","numAffected":0,"numAtRisk":2},{"groupId":"EG020","numAffected":0,"numAtRisk":2},{"groupId":"EG021","numAffected":0,"numAtRisk":1}],"term":"Lymphopenia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA v 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