The most commonly reported side effects of vorinostat include febrile neutropenia, product use in unapproved indication, and thrombocytopenia, based on 2,512 FDA adverse event reports from 2006 to 2025.
Percentages show how often each reaction appears relative to total reports for vorinostat.
These are voluntary reports and do not establish that vorinostat caused these reactions.
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Other drugs that appear in adverse event reports alongside vorinostat. 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.
38.5% of vorinostat adverse event reports involve female patients and 44.3% involve male patients. The largest age group is adult at 45%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking vorinostat when the adverse event was reported.
Showing 15 of 264 indications
Vorinostat is sold under the brand name Zolinza.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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