The most commonly reported side effects of futibatinib include diarrhoea, death, and disease progression, based on 183 FDA adverse event reports from 2021 to 2025.
Percentages show how often each reaction appears relative to total reports for futibatinib.
These are voluntary reports and do not establish that futibatinib caused these reactions.
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Other drugs that appear in adverse event reports alongside futibatinib. 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.
51.9% of futibatinib adverse event reports involve female patients and 39.9% involve male patients. The largest age group is adult at 60%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking futibatinib when the adverse event was reported.
Showing 15 of 33 indications
Futibatinib is sold under the brand name Lytgobi.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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