The most commonly reported side effects of defibrotide include off label use, venoocclusive disease, and death, based on 4,198 FDA adverse event reports from 2004 to 2025. 3.4% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for defibrotide.
These are voluntary reports and do not establish that defibrotide caused these reactions.
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Other drugs that appear in adverse event reports alongside defibrotide. Drugs flagged as a suspected cause appear in the first column. Drugs taken at the same time but not suspected appear in the second.
Also suspected
Taken alongside
Co-occurrence in adverse event reports does not establish a drug interaction. Patients often take multiple medications, and these lists reflect prescribing patterns rather than causal relationships. Consult a healthcare provider about potential drug interactions.
22.4% of defibrotide adverse event reports involve female patients and 34.4% involve male patients. The largest age group is adult at 55%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking defibrotide when the adverse event was reported.
Showing 15 of 107 indications
Defibrotide is sold under the brand name Defitelio.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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