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Mitoxangtrone FDA adverse reports: 1. View All Mitoxangtrone FDA Adverse Reports

Mitoxangtrone FDA safety alerts: No

Reported hospitalizations: 1

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Mitoxangtrone Side Effects Report: 5369887-2,Acute Myeloid Leukaemia, Blood Potassium Decreased, Capillary Leak Syndrome, Disease Progression, Fluid Overload, Leukocytosis, Lung Infiltration, Polyneuropathy, Respiratory Distress
on Jun 11, 2007 Male patient from UNITED STATES, , 29 years of age, was diagnosed with acute myeloid leukaemia and was treated with Mitoxangtrone. After Mitoxangtrone was administered, patient had the following side effects: Mitoxangtrone and acute myeloid leukaemia, Mitoxangtrone and blood potassium decreased, Mitoxangtrone and capillary leak syndrome, Mitoxangtrone and disease progression, Mitoxangtrone and fluid overload, Mitoxangtrone and leukocytosis, Mitoxangtrone and lung infiltration, Mitoxangtrone and polyneuropathy, Mitoxangtrone and respiratory distress. Mitoxangtrone dosage: . During the same period patient was treated with ARSENIC TRIOXIDE, IDARURICIN. Patient was hospitalized.


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During the same period patient was treated with MITOXANTRONE (See Image) (View Mitoxantrone Review and Mitoxantrone Label ). Patient was hospitalized.

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Mitoxangtrone Side Effects
Mitoxangtrone and Acute myeloid leukaemia
Mitoxangtrone and Blood potassium decreased
Mitoxangtrone and Capillary leak syndrome
Mitoxangtrone and Disease progression
Mitoxangtrone and Fluid overload
Mitoxangtrone and Leukocytosis
Mitoxangtrone and Lung infiltration
Mitoxangtrone and Polyneuropathy
Mitoxangtrone and Respiratory distress

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