The most commonly reported side effects of cedazuridine include death, inappropriate schedule of product administration, and fatigue, based on 663 FDA adverse event reports from 2005 to 2025.
Percentages show how often each reaction appears relative to total reports for cedazuridine.
These are voluntary reports and do not establish that cedazuridine caused these reactions.
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Other drugs that appear in adverse event reports alongside cedazuridine. 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.
35.9% of cedazuridine adverse event reports involve female patients and 50.8% involve male patients. The largest age group is elderly at 88%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking cedazuridine when the adverse event was reported.
Showing 15 of 63 indications
Cedazuridine is sold under the brand name Inqovi.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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