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Adverse events for arm \"Gemcitabine or Pralatrexate or Romidepsin\" were reported separately for each treatment received and reported as Gemcitabine, Pralatrexate, and Romidepsin.","eventGroups":[{"deathsNumAffected":11,"deathsNumAtRisk":137,"description":"Alisertib 50 mg, enteric-coated tablet formulation, orally, twice daily for 7 consecutive days (Cycle Days 1-7) in a 21-day cycle (Up to 148 Weeks).","id":"EG000","otherNumAffected":134,"otherNumAtRisk":137,"seriousNumAffected":75,"seriousNumAtRisk":137,"title":"Alisertib"},{"deathsNumAffected":5,"deathsNumAtRisk":29,"description":"Gemcitabine 1,000 mg/m\\^2 over 30 minutes, intravenously, on Days 1, 8, and 15 of a 28-day cycle until the absence of disease progression or unacceptable toxicity (Up to 32 Weeks).","id":"EG001","otherNumAffected":29,"otherNumAtRisk":29,"seriousNumAffected":18,"seriousNumAtRisk":29,"title":"Gemcitabine"},{"deathsNumAffected":8,"deathsNumAtRisk":76,"description":"Pralatrexate 30 mg/m\\^2, intravenous (IV) push over 3 to 5 minutes, once weekly, for 6 weeks in 7-week cycles with concurrent vitamin B12 and folic acid supplementation. Cycles were repeated every 7-weeks provided the participant continued to benefit from and tolerate the therapy (Up to 115 Weeks).","id":"EG002","otherNumAffected":72,"otherNumAtRisk":76,"seriousNumAffected":46,"seriousNumAtRisk":76,"title":"Pralatrexate"},{"deathsNumAffected":2,"deathsNumAtRisk":22,"description":"Romidepsin 14 mg/m\\^2, intravenously over a 4-hour period, on Days 1, 8, and 15 of a 28-cycle. Cycles were repeated every 28 days provided the patient continued to benefit from and tolerate the therapy (Up to 30 Weeks).","id":"EG003","otherNumAffected":21,"otherNumAtRisk":22,"seriousNumAffected":6,"seriousNumAtRisk":22,"title":"Romidepsin"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA version 15.0","stats":[{"groupId":"EG000","numAffected":61,"numAtRisk":137},{"groupId":"EG001","numAffected":5,"numAtRisk":29},{"groupId":"EG002","numAffected":18,"numAtRisk":76},{"groupId":"EG003","numAffected":10,"numAtRisk":22}],"term":"Diarrhoea"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA version 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