The most commonly reported side effects of axitinib include death, diarrhoea, and fatigue, based on 19,006 FDA adverse event reports from 2008 to 2025.
Percentages show how often each reaction appears relative to total reports for axitinib.
These are voluntary reports and do not establish that axitinib caused these reactions.
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Other drugs that appear in adverse event reports alongside axitinib. 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.
27.0% of axitinib adverse event reports involve female patients and 65.3% involve male patients. The largest age group is elderly at 55%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking axitinib when the adverse event was reported.
Showing 15 of 442 indications
Axitinib is sold under the brand name Axitinib.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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