The most commonly reported side effects of enzalutamide include fatigue, death, and malignant neoplasm progression, based on 57,858 FDA adverse event reports from 2012 to 2025. 7.0% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for enzalutamide.
These are voluntary reports and do not establish that enzalutamide caused these reactions.
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Other drugs that appear in adverse event reports alongside enzalutamide. 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.
0.6% of enzalutamide adverse event reports involve female patients and 95.3% involve male patients. The largest age group is elderly at 86%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking enzalutamide when the adverse event was reported.
Showing 15 of 366 indications
Enzalutamide is sold under the brand name Enzalutamide.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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