Vyxeos is supplied in a single dose vial containing 44 mg of daunorubicin and 100 mg of cytarabine1

  • Prior to initiating each cycle, calculate the prior cumulative anthracycline exposure for the patient
  • Assess cardiac function, complete blood counts, and liver and renal function before each consolidation cycle
  • Do not start consolidation until the absolute neutrophil count recovers to greater than 0.5 Gi/L and the platelet count recovers to greater than 50 Gi/L in the absence of unacceptable toxicity
  • Administer the second consolidation cycle 5 to 8 weeks after the start of the first consolidation cycle in patients who do not show disease progression on unacceptable toxicity


  1. Vyxeos summary of product characteristics





Reporting of side effects: Adverse events should be reported. Healthcare professionals are asked to report any suspected adverse reactions via their national reporting system. In the United Kingdom, reporting forms and information can be found at Adverse events should also be reported by email: or by fax to +44 (0) 1865 598765



EURW-INTVYX-0020a(1) | September 2019