{"description":"A serious adverse event (SAE) is any untoward medical occurrence after study treatment initiation that results in death, is life-threatening, requires or prolongs hospitalization, causes disability/incapacity, is a congenital anomaly, or, based on medical judgment, may jeopardize the patient or require intervention to prevent serious outcomes.","eventGroups":[{"deathsNumAffected":23,"deathsNumAtRisk":90,"description":"Induction: Daunorubicin, cytarabine and gilteritinib. 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