The most commonly reported side effects of taletrectinib include diarrhoea, vomiting, and nausea, based on 27 FDA adverse event reports from 2025 to 2025.
Percentages show how often each reaction appears relative to total reports for taletrectinib.
These are voluntary reports and do not establish that taletrectinib caused these reactions.
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Other drugs that appear in adverse event reports alongside taletrectinib. Drugs flagged as a suspected cause appear in the first column. Drugs taken at the same time but not suspected appear in the second.
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 taletrectinib adverse event reports involve female patients and 33.3% involve male patients. The largest age group is adult at 56%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking taletrectinib when the adverse event was reported.
Taletrectinib is sold under the brand name Ibtrozi.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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