{"description":"Participants who received at least one dose of study intervention. Based on the planned safety analysis, adverse events were collected and reported by treatment regimen.\n\nGender specific events only occurring in male or female participants have had the number of participants \"At Risk\" adjusted accordingly.","eventGroups":[{"deathsNumAffected":4,"deathsNumAtRisk":4,"description":"Participants received 0.08 or 0.1 mg of Pegilodecakin once daily (QD) administered subcutaneously (SC).\n\nStudy treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG000","otherNumAffected":4,"otherNumAtRisk":4,"seriousNumAffected":3,"seriousNumAtRisk":4,"title":"Part A: Pegilodecakin 0.08/0.1 mg"},{"deathsNumAffected":6,"deathsNumAtRisk":6,"description":"Participants received 0.2 or 0.25 mg dose of Pegilodecakin QD administered SC Study treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG001","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":2,"seriousNumAtRisk":6,"title":"Part A: Pegilodecakin 0.2/0.25 mg"},{"deathsNumAffected":6,"deathsNumAtRisk":6,"description":"Participants received 0.4 or 0.5 mg dose of Pegilodecakin QD administered SC. Study treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG002","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":2,"seriousNumAtRisk":6,"title":"Part A: Pegilodecakin 0.4/0.5 mg"},{"deathsNumAffected":6,"deathsNumAtRisk":6,"description":"Participants received 0.8 or 1 mg of Pegilodecakin QD administered SC Study treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG003","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":2,"seriousNumAtRisk":6,"title":"Part A: Pegilodecakin 0.8/1 mg"},{"deathsNumAffected":105,"deathsNumAtRisk":117,"description":"Participants received 1.6 or 2 mg of Pegilodecakin QD administered SC Study treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG004","otherNumAffected":116,"otherNumAtRisk":117,"seriousNumAffected":60,"seriousNumAtRisk":117,"title":"Part A: Pegilodecakin 1.6/2 mg"},{"deathsNumAffected":5,"deathsNumAtRisk":5,"description":"Participants received 3.2 or 4 mg of Pegilodecakin QD administered SC Study treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG005","otherNumAffected":5,"otherNumAtRisk":5,"seriousNumAffected":2,"seriousNumAtRisk":5,"title":"Part A: Pegilodecakin 3.2/4 mg"},{"deathsNumAffected":4,"deathsNumAtRisk":4,"description":"Participants received 0.2 or 0.25 mg of Pegilodecakin QD administered SC along with Platinum/Taxane combination on Day 1 of each 21-day cycle for a maximum of 5 or 6 cycles. Participants received:\n\nPaclitaxel 200 or 175 mg/m² intravenously (IV) over 3 hours, or docetaxel 75 or 65 mg/m² IV over 1 hour, followed by carboplatin (AUC 6/5/4; max 6 × 150 mg) IV over 30 minutes or cisplatin 75 mg/m² IV over 6-8 hours.\n\nStudy treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG006","otherNumAffected":4,"otherNumAtRisk":4,"seriousNumAffected":0,"seriousNumAtRisk":4,"title":"Part B: Pegilodecakin 0.2/0.25 mg + Platinum/Taxane"},{"deathsNumAffected":3,"deathsNumAtRisk":3,"description":"Participants received 0.4 or 0.5 mg of Pegilodecakin QD administered SC along with Platinum/Taxane combination on Day 1 of each 21-day cycle for a maximum of 5 or 6 cycles. Participants received:\n\nPaclitaxel 200 or 175 mg/m² intravenously (IV) over 3 hours, or docetaxel 75 or 65 mg/m² IV over 1 hour, followed by carboplatin (AUC 6/5/4; max 6 × 150 mg) IV over 30 minutes or cisplatin 75 mg/m² IV over 6-8 hours.\n\nStudy treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG007","otherNumAffected":3,"otherNumAtRisk":3,"seriousNumAffected":1,"seriousNumAtRisk":3,"title":"Part B: Pegilodecakin 0.4/0.5 mg + Platinum/Taxane"},{"deathsNumAffected":14,"deathsNumAtRisk":18,"description":"Participants received 0.8 or 1 mg of Pegilodecakin QD administered SC along with Platinum/Taxane combination on Day 1 of each 21-day cycle for a maximum of 5 or 6 cycles. Participants received:\n\nPaclitaxel 200 or 175 mg/m² intravenously (IV) over 3 hours, or docetaxel 75 or 65 mg/m² IV over 1 hour, followed by carboplatin (AUC 6/5/4; max 6 × 150 mg) IV over 30 minutes or cisplatin 75 mg/m² IV over 6-8 hours.\n\nStudy treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG008","otherNumAffected":18,"otherNumAtRisk":18,"seriousNumAffected":10,"seriousNumAtRisk":18,"title":"Part B: Pegilodecakin 0.8/1 mg + Platinum/Taxane"},{"deathsNumAffected":4,"deathsNumAtRisk":4,"description":"Participants received 0.2 or 0.25 mg dose of Pegilodecakin QD administered SC and FOLFOX treatment on Day 1 of each 14-day cycle for a maximum of 12 cycles. Participants received:\n\noxaliplatin 85 mg/m2 IV over 2 hours, and leucovorin 200 mg/m2 IV over 2 hours, followed by 5-FU 400 mg/m2 IV bolus over 2-4 minutes, 5-FU 600 mg/m2/day IV over 22 hours, and leucovorin 200 mg/m2 over 2 hours on Day 2 followed by 5-FU 400 mg/m2 IV bolus over 2-4 minutes, and 5-FU 600 mg/m2/day IV over 22 hours.\n\nStudy treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG009","otherNumAffected":4,"otherNumAtRisk":4,"seriousNumAffected":3,"seriousNumAtRisk":4,"title":"Part C: Pegilodecakin 0.2/0.25 mg + FOLFOX"},{"deathsNumAffected":27,"deathsNumAtRisk":29,"description":"Participants received 0.4 or 0.5 mg of Pegilodecakin QD administered SC and FOLFOX treatment on Day 1 of each 14-day cycle for a maximum of 12 cycles. Participants received:\n\noxaliplatin 85 mg/m2 IV over 2 hours, and leucovorin 200 mg/m2 IV over 2 hours, followed by 5-FU 400 mg/m2 IV bolus over 2-4 minutes, 5-FU 600 mg/m2/day IV over 22 hours, and leucovorin 200 mg/m2 over 2 hours on Day 2 followed by 5-FU 400 mg/m2 IV bolus over 2-4 minutes, and 5-FU 600 mg/m2/day IV over 22 hours.\n\nStudy treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG010","otherNumAffected":29,"otherNumAtRisk":29,"seriousNumAffected":14,"seriousNumAtRisk":29,"title":"Part C: Pegilodecakin 0.4/0.5 mg + FOLFOX"},{"deathsNumAffected":6,"deathsNumAtRisk":6,"description":"Participants received 0.8 or 1 mg dose of Pegilodecakin QD administered SC and FOLFOX treatment on Day 1 of each 14-day cycle for a maximum of 12 cycles. Participants received:\n\noxaliplatin 85 mg/m2 IV over 2 hours, and leucovorin 200 mg/m2 IV over 2 hours, followed by 5-FU 400 mg/m2 IV bolus over 2-4 minutes, 5-FU 600 mg/m2/day IV over 22 hours, and leucovorin 200 mg/m2 over 2 hours on Day 2 followed by 5-FU 400 mg/m2 IV bolus over 2-4 minutes, and 5-FU 600 mg/m2/day IV over 22 hours.\n\nStudy treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG011","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":3,"seriousNumAtRisk":6,"title":"Part C: Pegilodecakin 0.8/1 mg + FOLFOX"},{"deathsNumAffected":6,"deathsNumAtRisk":6,"description":"Participants received 0.4 or 0.5 mg of Pegilodecakin QD administered SC with Gemcitabine 1000 mg/m2 IV over 30 minutes plus nab-paclitaxel 125 mg/m2 IV over 30 to 40 minutes on Days 1, 8, and 15 of every 28-day cycle.\n\nStudy treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG012","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":2,"seriousNumAtRisk":6,"title":"Part D: Pegilodecakin 0.4/0.5 mg + Gemcitabine/Nab-Paclitaxel"},{"deathsNumAffected":6,"deathsNumAtRisk":6,"description":"Participants received 0.8 or 1 mg of Pegilodecakin QD administered SC with Capecitabine 1000 mg/m² orally twice daily (BID) on Days 1 through 14 of each 21-day cycle.\n\nStudy treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG013","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":4,"seriousNumAtRisk":6,"title":"Part E: Pegilodecakin 0.8/1 mg + Capecitabine"},{"deathsNumAffected":6,"deathsNumAtRisk":6,"description":"Participants received 0.8 or 1 mg of Pegilodecakin QD administered SC with Paclitaxel 80 mg/m2 IV over 3 hours on Days 1, 8, and 15 of every 28-day cycle.\n\nStudy treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG014","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":4,"seriousNumAtRisk":6,"title":"Part F: Pegilodecakin 0.8/1 mg + Paclitaxel"},{"deathsNumAffected":4,"deathsNumAtRisk":6,"description":"Participants received a 0.8 or 1 mg of Pegilodecakin QD administered SC with Pazopanib 800 mg orally QD.\n\nStudy treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG015","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":1,"seriousNumAtRisk":6,"title":"Part G: Pegilodecakin 0.8/1 mg + Pazopanib"},{"deathsNumAffected":8,"deathsNumAtRisk":14,"description":"Participants received 0.8 or 1 mg of Pegilodecakin QD administered SC with Pembrolizumab 2 mg/kg bolus IV infusion over 30 minutes on Day 1 of each 21-day cycle.\n\nStudy treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG016","otherNumAffected":14,"otherNumAtRisk":14,"seriousNumAffected":8,"seriousNumAtRisk":14,"title":"Part H: Pegilodecakin 0.8/1 mg + Pembrolizumab"},{"deathsNumAffected":29,"deathsNumAtRisk":34,"description":"Participants received 1.6 or 2 mg of Pegilodecakin QD administered SC with Pembrolizumab 2 mg/kg bolus IV infusion over 30 minutes on Day 1 of each 21-day cycle.\n\nStudy treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG017","otherNumAffected":34,"otherNumAtRisk":34,"seriousNumAffected":16,"seriousNumAtRisk":34,"title":"Part H: Pegilodecakin 1.6/2 mg + Pembrolizumab"},{"deathsNumAffected":3,"deathsNumAtRisk":5,"description":"Participants received 3.2 or 4 mg of Pegilodecakin QD administered SC with Pembrolizumab 2 mg/kg bolus IV infusion over 30 minutes on Day 1 of each 21-day cycle.\n\nStudy treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG018","otherNumAffected":5,"otherNumAtRisk":5,"seriousNumAffected":3,"seriousNumAtRisk":5,"title":"Part H: Pegilodecakin 3.2/4 mg + Pembrolizumab"},{"deathsNumAffected":0,"deathsNumAtRisk":1,"description":"Participants received 0.8 or 1 mg of Pegilodecakin QD administered SC with Nivolumab 3 mg/kg IV infusion over 60 minutes on Day 1 of each 14-day cycle.\n\nStudy treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG019","otherNumAffected":1,"otherNumAtRisk":1,"seriousNumAffected":1,"seriousNumAtRisk":1,"title":"Part I: Pegilodecakin 0.8/1 mg + Nivolumab"},{"deathsNumAffected":33,"deathsNumAtRisk":57,"description":"Participants received 1.6 or 2 mg of Pegilodecakin QD administered SC with Nivolumab 3 mg/kg IV infusion over 60 minutes on Day 1 of each 14-day cycle.\n\nStudy treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG020","otherNumAffected":56,"otherNumAtRisk":57,"seriousNumAffected":32,"seriousNumAtRisk":57,"title":"Part I: Pegilodecakin 1.6/2 mg + Nivolumab"},{"deathsNumAffected":5,"deathsNumAtRisk":5,"description":"Participants received 0.4 or 0.5 mg of Pegilodecakin QD administered SC with gemcitabine 500 mg/m2 IV over 30 minutes followed by carboplatin targeting an AUC2 IV over 60 minutes on Days 1 and 8 of each 21-day cycle.\n\nStudy treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG021","otherNumAffected":5,"otherNumAtRisk":5,"seriousNumAffected":2,"seriousNumAtRisk":5,"title":"Part J: Pegilodecakin 0.4/0.5 mg + Gemcitabine/Carboplatin"},{"deathsNumAffected":5,"deathsNumAtRisk":5,"description":"Participants received 0.8 or 1 mg of Pegilodecakin QD administered SC with gemcitabine 500 mg/m2 IV over 30 minutes followed by carboplatin targeting an AUC2 IV over 60 minutes on Days 1 and 8 of each 21-day cycle.\n\nStudy treatment continued until disease progression, death, unacceptable toxicity, or end of trial.","id":"EG022","otherNumAffected":5,"otherNumAtRisk":5,"seriousNumAffected":1,"seriousNumAtRisk":5,"title":"Part J: Pegilodecakin 0.8/1 mg + Gemcitabine/Carboplatin"}],"frequencyThreshold":"0","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 28.1","stats":[{"groupId":"EG000","numAffected":2,"numAtRisk":4,"numEvents":2},{"groupId":"EG001","numAffected":3,"numAtRisk":6,"numEvents":3},{"groupId":"EG002","numAffected":5,"numAtRisk":6,"numEvents":5},{"groupId":"EG003","numAffected":5,"numAtRisk":6,"numEvents":5},{"groupId":"EG004","numAffected":88,"numAtRisk":117,"numEvents":88},{"groupId":"EG005","numAffected":4,"numAtRisk":5,"numEvents":4},{"groupId":"EG006","numAffected":3,"numAtRisk":4,"numEvents":3},{"groupId":"EG007","numAffected":3,"numAtRisk":3,"numEvents":3},{"groupId":"EG008","numAffected":14,"numAtRisk":18,"numEvents":14},{"groupId":"EG009","numAffected":2,"numAtRisk":4,"numEvents":2},{"groupId":"EG010","numAffected":19,"numAtRisk":29,"numEvents":19},{"groupId":"EG011","numAffected":4,"numAtRisk":6,"numEvents":4},{"groupId":"EG012","numAffected":2,"numAtRisk":6,"numEvents":2},{"groupId":"EG013","numAffected":5,"numAtRisk":6,"numEvents":5},{"groupId":"EG014","numAffected":5,"numAtRisk":6,"numEvents":5},{"groupId":"EG015","numAffected":1,"numAtRisk":6,"numEvents":1},{"groupId":"EG016","numAffected":8,"numAtRisk":14,"numEvents":8},{"groupId":"EG017","numAffected":26,"numAtRisk":34,"numEvents":26},{"groupId":"EG018","numAffected":4,"numAtRisk":5,"numEvents":4},{"groupId":"EG019","numAffected":1,"numAtRisk":1,"numEvents":1},{"groupId":"EG020","numAffected":39,"numAtRisk":57,"numEvents":39},{"groupId":"EG021","numAffected":4,"numAtRisk":5,"numEvents":4},{"groupId":"EG022","numAffected":5,"numAtRisk":5,"numEvents":5}],"term":"Anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 28.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":4,"numEvents":0},{"groupId":"EG001","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG002","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG003","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG004","numAffected":0,"numAtRisk":117,"numEvents":0},{"groupId":"EG005","numAffected":0,"numAtRisk":5,"numEvents":0},{"groupId":"EG006","numAffected":0,"numAtRisk":4,"numEvents":0},{"groupId":"EG007","numAffected":0,"numAtRisk":3,"numEvents":0},{"groupId":"EG008","numAffected":0,"numAtRisk":18,"numEvents":0},{"groupId":"EG009","numAffected":0,"numAtRisk":4,"numEvents":0},{"groupId":"EG010","numAffected":0,"numAtRisk":29,"numEvents":0},{"groupId":"EG011","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG012","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG013","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG014","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG015","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG016","numAffected":0,"numAtRisk":14,"numEvents":0},{"groupId":"EG017","numAffected":0,"numAtRisk":34,"numEvents":0},{"groupId":"EG018","numAffected":0,"numAtRisk":5,"numEvents":0},{"groupId":"EG019","numAffected":0,"numAtRisk":1,"numEvents":0},{"groupId":"EG020","numAffected":1,"numAtRisk":57,"numEvents":1},{"groupId":"EG021","numAffected":0,"numAtRisk":5,"numEvents":0},{"groupId":"EG022","numAffected":0,"numAtRisk":5,"numEvents":0}],"term":"Anisocytosis"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 28.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":4,"numEvents":0},{"groupId":"EG001","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG002","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG003","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG004","numAffected":1,"numAtRisk":117,"numEvents":1},{"groupId":"EG005","numAffected":0,"numAtRisk":5,"numEvents":0},{"groupId":"EG006","numAffected":0,"numAtRisk":4,"numEvents":0},{"groupId":"EG007","numAffected":0,"numAtRisk":3,"numEvents":0},{"groupId":"EG008","numAffected":0,"numAtRisk":18,"numEvents":0},{"groupId":"EG009","numAffected":0,"numAtRisk":4,"numEvents":0},{"groupId":"EG010","numAffected":0,"numAtRisk":29,"numEvents":0},{"groupId":"EG011","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG012","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG013","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG014","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG015","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG016","numAffected":0,"numAtRisk":14,"numEvents":0},{"groupId":"EG017","numAffected":0,"numAtRisk":34,"numEvents":0},{"groupId":"EG018","numAffected":0,"numAtRisk":5,"numEvents":0},{"groupId":"EG019","numAffected":0,"numAtRisk":1,"numEvents":0},{"groupId":"EG020","numAffected":0,"numAtRisk":57,"numEvents":0},{"groupId":"EG021","numAffected":0,"numAtRisk":5,"numEvents":0},{"groupId":"EG022","numAffected":0,"numAtRisk":5,"numEvents":0}],"term":"Coagulopathy"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 28.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":4,"numEvents":0},{"groupId":"EG001","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG002","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG003","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG004","numAffected":0,"numAtRisk":117,"numEvents":0},{"groupId":"EG005","numAffected":0,"numAtRisk":5,"numEvents":0},{"groupId":"EG006","numAffected":0,"numAtRisk":4,"numEvents":0},{"groupId":"EG007","numAffected":0,"numAtRisk":3,"numEvents":0},{"groupId":"EG008","numAffected":0,"numAtRisk":18,"numEvents":0},{"groupId":"EG009","numAffected":0,"numAtRisk":4,"numEvents":0},{"groupId":"EG010","numAffected":0,"numAtRisk":29,"numEvents":0},{"groupId":"EG011","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG012","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG013","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG014","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG015","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG016","numAffected":0,"numAtRisk":14,"numEvents":0},{"groupId":"EG017","numAffected":0,"numAtRisk":34,"numEvents":0},{"groupId":"EG018","numAffected":0,"numAtRisk":5,"numEvents":0},{"groupId":"EG019","numAffected":0,"numAtRisk":1,"numEvents":0},{"groupId":"EG020","numAffected":1,"numAtRisk":57,"numEvents":1},{"groupId":"EG021","numAffected":0,"numAtRisk":5,"numEvents":0},{"groupId":"EG022","numAffected":0,"numAtRisk":5,"numEvents":0}],"term":"Increased tendency to bruise"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 28.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":4,"numEvents":0},{"groupId":"EG001","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG002","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG003","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG004","numAffected":3,"numAtRisk":117,"numEvents":3},{"groupId":"EG005","numAffected":0,"numAtRisk":5,"numEvents":0},{"groupId":"EG006","numAffected":0,"numAtRisk":4,"numEvents":0},{"groupId":"EG007","numAffected":0,"numAtRisk":3,"numEvents":0},{"groupId":"EG008","numAffected":0,"numAtRisk":18,"numEvents":0},{"groupId":"EG009","numAffected":0,"numAtRisk":4,"numEvents":0},{"groupId":"EG010","numAffected":0,"numAtRisk":29,"numEvents":0},{"groupId":"EG011","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG012","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG013","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG014","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG015","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG016","numAffected":0,"numAtRisk":14,"numEvents":0},{"groupId":"EG017","numAffected":0,"numAtRisk":34,"numEvents":0},{"groupId":"EG018","numAffected":0,"numAtRisk":5,"numEvents":0},{"groupId":"EG019","numAffected":0,"numAtRisk":1,"numEvents":0},{"groupId":"EG020","numAffected":2,"numAtRisk":57,"numEvents":2},{"groupId":"EG021","numAffected":0,"numAtRisk":5,"numEvents":0},{"groupId":"EG022","numAffected":0,"numAtRisk":5,"numEvents":0}],"term":"Iron deficiency anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 28.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":4,"numEvents":1},{"groupId":"EG001","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG002","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG003","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG004","numAffected":9,"numAtRisk":117,"numEvents":9},{"groupId":"EG005","numAffected":1,"numAtRisk":5,"numEvents":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4,"numEvents":0},{"groupId":"EG007","numAffected":0,"numAtRisk":3,"numEvents":0},{"groupId":"EG008","numAffected":5,"numAtRisk":18,"numEvents":5},{"groupId":"EG009","numAffected":0,"numAtRisk":4,"numEvents":0},{"groupId":"EG010","numAffected":1,"numAtRisk":29,"numEvents":1},{"groupId":"EG011","numAffected":2,"numAtRisk":6,"numEvents":2},{"groupId":"EG012","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG013","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG014","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG015","numAffected":0,"numAtRisk":6,"numEvents":0},{"groupId":"EG016","numAffected":1,"numAtRisk":14,"numEvents":1},{"groupId":"EG017","numAffected":0,"numAtRisk":34,"numEvents":0},{"groupId":"EG018","numAffected":1,"numAtRisk":5,"numEvents":1},{"groupId":"EG019","numAffected":0,"numAtRisk":1,"numEvents":0},{"groupId":"EG020","numAffected":4,"numAtRisk":57,"numEvents":4},{"groupId":"EG021","numAffected":0,"numAtRisk":5,"numEvents":0},{"groupId":"EG022","numAffected":1,"numAtRisk":5,"numEvents":1}],"term":"Leukocytosis"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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