The most commonly reported side effects of tipiracil include death, disease progression, and fatigue, based on 10,453 FDA adverse event reports from 2015 to 2025. 3.5% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for tipiracil.
These are voluntary reports and do not establish that tipiracil caused these reactions.
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Seriousness is determined by the reporter, not by OpenClaim.
Other drugs that appear in adverse event reports alongside tipiracil. 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.
41.0% of tipiracil adverse event reports involve female patients and 56.8% involve male patients. The largest age group is adult at 50%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking tipiracil when the adverse event was reported.
Showing 15 of 232 indications
Tipiracil is sold under the brand name Trifluridine; Tipiracil.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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