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Otherwise, zero means that the term is part of the MedDRA version but no events were observed.\n\nIncluded in MedDRA 25.1 but not in MedDRA 27.0: Myxoedema coma Included in MedDRA 27.0 but not in MedDRA 25.1: Bile acids increased","eventGroups":[{"deathsNumAffected":82,"deathsNumAtRisk":241,"description":"Platinum-based chemotherapy (paclitaxel and carboplatin) Q3W for a maximum of 6 cycles with durvalumab placebo (IV) Q3W.\n\nFollowing completion of chemotherapy treatment, patients without objective disease progression received durvalumab placebo (IV) Q4W and olaparib placebo (tablets) twice bd orally as maintenance treatment until disease progression.","id":"EG000","otherNumAffected":233,"otherNumAtRisk":236,"seriousNumAffected":73,"seriousNumAtRisk":236,"title":"Global Cohort - SoC"},{"deathsNumAffected":65,"deathsNumAtRisk":238,"description":"Platinum-based chemotherapy (paclitaxel and carboplatin) Q3W for a maximum of 6 cycles with 1120 mg durvalumab (IV) Q3W.\n\nFollowing completion of chemotherapy treatment, patients without objective disease progression received 1500 mg durvalumab (IV) Q4W with olaparib placebo (tablets) bd orally as maintenance treatment until disease progression.","id":"EG001","otherNumAffected":228,"otherNumAtRisk":235,"seriousNumAffected":73,"seriousNumAtRisk":235,"title":"Global Cohort - SoC + Durvalumab"},{"deathsNumAffected":52,"deathsNumAtRisk":239,"description":"Platinum-based chemotherapy (paclitaxel and carboplatin) Q3W for a maximum of 6 cycles with 1120 mg durvalumab (IV) Q3W.\n\nFollowing completion of chemotherapy treatment, patients without objective disease progression received 1500 mg durvalumab (IV) Q4W with 300 mg olaparib (tablets) bd orally as maintenance treatment until disease progression.","id":"EG002","otherNumAffected":236,"otherNumAtRisk":238,"seriousNumAffected":85,"seriousNumAtRisk":238,"title":"Global Cohort - SoC + Durvalumab + Olaparib"},{"deathsNumAffected":12,"deathsNumAtRisk":44,"description":"Platinum-based chemotherapy (paclitaxel and carboplatin) Q3W for a maximum of 6 cycles with durvalumab placebo (IV) Q3W.\n\nFollowing completion of chemotherapy treatment, participants without objective disease progression received durvalumab placebo (IV) Q4W and olaparib placebo (tablets) twice bd orally as maintenance treatment until disease progression.","id":"EG003","otherNumAffected":44,"otherNumAtRisk":44,"seriousNumAffected":14,"seriousNumAtRisk":44,"title":"China Cohort - SoC"},{"deathsNumAffected":11,"deathsNumAtRisk":43,"description":"Platinum-based chemotherapy (paclitaxel and carboplatin) Q3W for a maximum of 6 cycles with 1120 mg durvalumab (IV) Q3W.\n\nFollowing completion of chemotherapy treatment, participants without objective disease progression received 1500 mg durvalumab (IV) Q4W with olaparib placebo (tablets) bd orally as maintenance treatment until disease progression.","id":"EG004","otherNumAffected":41,"otherNumAtRisk":41,"seriousNumAffected":8,"seriousNumAtRisk":41,"title":"China Cohort - SoC + Durvalumab"},{"deathsNumAffected":14,"deathsNumAtRisk":42,"description":"Platinum-based chemotherapy (paclitaxel and carboplatin) Q3W for a maximum of 6 cycles with 1120 mg durvalumab (IV) Q3W.\n\nFollowing completion of chemotherapy treatment, patients without objective disease progression received 1500 mg durvalumab (IV) Q4W with 300 mg olaparib (tablets) bd orally as maintenance treatment until disease progression.","id":"EG005","otherNumAffected":39,"otherNumAtRisk":41,"seriousNumAffected":19,"seriousNumAtRisk":41,"title":"China Cohort - SoC + Durvalumab + Olaparib"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Infections and infestations","sourceVocabulary":"MedDRA 25.1, 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infection"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Infections and infestations","sourceVocabulary":"MedDRA 25.1, 27.0","stats":[{"groupId":"EG000","numAffected":47,"numAtRisk":236,"numEvents":65},{"groupId":"EG001","numAffected":32,"numAtRisk":235,"numEvents":62},{"groupId":"EG002","numAffected":46,"numAtRisk":238,"numEvents":67},{"groupId":"EG003","numAffected":8,"numAtRisk":44,"numEvents":12},{"groupId":"EG004","numAffected":4,"numAtRisk":41,"numEvents":10},{"groupId":"EG005","numAffected":5,"numAtRisk":41,"numEvents":8}],"term":"Urinary tract infection"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 25.1, 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27.0","stats":[{"groupId":"EG000","numAffected":10,"numAtRisk":236,"numEvents":10},{"groupId":"EG001","numAffected":14,"numAtRisk":235,"numEvents":14},{"groupId":"EG002","numAffected":15,"numAtRisk":238,"numEvents":19},{"groupId":"EG003","numAffected":0,"numAtRisk":44,"numEvents":0},{"groupId":"EG004","numAffected":0,"numAtRisk":41,"numEvents":0},{"groupId":"EG005","numAffected":0,"numAtRisk":41,"numEvents":0}],"term":"Fall"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Injury, poisoning and procedural complications","sourceVocabulary":"MedDRA 25.1, 27.0","stats":[{"groupId":"EG000","numAffected":22,"numAtRisk":236,"numEvents":28},{"groupId":"EG001","numAffected":14,"numAtRisk":235,"numEvents":19},{"groupId":"EG002","numAffected":12,"numAtRisk":238,"numEvents":17},{"groupId":"EG003","numAffected":1,"numAtRisk":44,"numEvents":2},{"groupId":"EG004","numAffected":1,"numAtRisk":41,"numEvents":1},{"groupId":"EG005","numAffected":2,"numAtRisk":41,"numEvents":2}],"term":"Infusion related reaction"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Investigations","sourceVocabulary":"MedDRA 25.1, 27.0","stats":[{"groupId":"EG000","numAffected":18,"numAtRisk":236,"numEvents":24},{"groupId":"EG001","numAffected":30,"numAtRisk":235,"numEvents":37},{"groupId":"EG002","numAffected":30,"numAtRisk":238,"numEvents":41},{"groupId":"EG003","numAffected":17,"numAtRisk":44,"numEvents":33},{"groupId":"EG004","numAffected":16,"numAtRisk":41,"numEvents":28},{"groupId":"EG005","numAffected":11,"numAtRisk":41,"numEvents":22}],"term":"Alanine aminotransferase increased"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Investigations","sourceVocabulary":"MedDRA 25.1, 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acids increased"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Investigations","sourceVocabulary":"MedDRA 25.1, 27.0","stats":[{"groupId":"EG000","numAffected":6,"numAtRisk":236,"numEvents":8},{"groupId":"EG001","numAffected":11,"numAtRisk":235,"numEvents":13},{"groupId":"EG002","numAffected":8,"numAtRisk":238,"numEvents":9},{"groupId":"EG003","numAffected":4,"numAtRisk":44,"numEvents":4},{"groupId":"EG004","numAffected":5,"numAtRisk":41,"numEvents":7},{"groupId":"EG005","numAffected":5,"numAtRisk":41,"numEvents":6}],"term":"Blood alkaline phosphatase increased"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Investigations","sourceVocabulary":"MedDRA 25.1, 27.0","stats":[{"groupId":"EG000","numAffected":4,"numAtRisk":236,"numEvents":7},{"groupId":"EG001","numAffected":4,"numAtRisk":235,"numEvents":7},{"groupId":"EG002","numAffected":0,"numAtRisk":238,"numEvents":0},{"groupId":"EG003","numAffected":5,"numAtRisk":44,"numEvents":8},{"groupId":"EG004","numAffected":1,"numAtRisk":41,"numEvents":1},{"groupId":"EG005","numAffected":4,"numAtRisk":41,"numEvents":8}],"term":"Blood bilirubin increased"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Investigations","sourceVocabulary":"MedDRA 25.1, 27.0","stats":[{"groupId":"EG000","numAffected":13,"numAtRisk":236,"numEvents":20},{"groupId":"EG001","numAffected":10,"numAtRisk":235,"numEvents":13},{"groupId":"EG002","numAffected":24,"numAtRisk":238,"numEvents":42},{"groupId":"EG003","numAffected":2,"numAtRisk":44,"numEvents":3},{"groupId":"EG004","numAffected":4,"numAtRisk":41,"numEvents":7},{"groupId":"EG005","numAffected":10,"numAtRisk":41,"numEvents":21}],"term":"Blood creatinine increased"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Investigations","sourceVocabulary":"MedDRA 25.1, 27.0","stats":[{"groupId":"EG000","numAffected":14,"numAtRisk":236,"numEvents":19},{"groupId":"EG001","numAffected":9,"numAtRisk":235,"numEvents":15},{"groupId":"EG002","numAffected":8,"numAtRisk":238,"numEvents":14},{"groupId":"EG003","numAffected":4,"numAtRisk":44,"numEvents":5},{"groupId":"EG004","numAffected":5,"numAtRisk":41,"numEvents":8},{"groupId":"EG005","numAffected":7,"numAtRisk":41,"numEvents":10}],"term":"Blood lactate dehydrogenase increased"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Investigations","sourceVocabulary":"MedDRA 25.1, 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