The most commonly reported side effects of vorasidenib include alanine aminotransferase increased, aspartate aminotransferase increased, and fatigue, based on 348 FDA adverse event reports from 2023 to 2025.
Percentages show how often each reaction appears relative to total reports for vorasidenib.
These are voluntary reports and do not establish that vorasidenib caused these reactions.
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Other drugs that appear in adverse event reports alongside vorasidenib. 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.
0.9% of vorasidenib adverse event reports involve female patients and 2.3% involve male patients. The largest age group is adult at 75%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking vorasidenib when the adverse event was reported.
Showing 15 of 20 indications
Vorasidenib is sold under the brand name Voranigo.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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