The most commonly reported side effects of vemurafenib include rash, arthralgia, and fatigue, based on 11,922 FDA adverse event reports from 2006 to 2025.
Percentages show how often each reaction appears relative to total reports for vemurafenib.
These are voluntary reports and do not establish that vemurafenib caused these reactions.
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Other drugs that appear in adverse event reports alongside vemurafenib. 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.
39.3% of vemurafenib adverse event reports involve female patients and 50.7% involve male patients. The largest age group is adult at 58%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking vemurafenib when the adverse event was reported.
Showing 15 of 401 indications
Vemurafenib is sold under the brand name Zelboraf.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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