The most commonly reported side effects of deferasirox include death, death, and diarrhoea, based on 26,755 FDA adverse event reports from 2005 to 2025.
Percentages show how often each reaction appears relative to total reports for deferasirox.
These are voluntary reports and do not establish that deferasirox caused these reactions.
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Other drugs that appear in adverse event reports alongside deferasirox. 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.
44.8% of deferasirox adverse event reports involve female patients and 46.2% involve male patients. The largest age group is elderly at 43%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking deferasirox when the adverse event was reported.
Showing 15 of 477 indications
Deferasirox is sold under the brand name Jadenu.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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