The most commonly reported side effects of capivasertib include diarrhoea, rash, and death, based on 2,056 FDA adverse event reports from 2020 to 2025.
Percentages show how often each reaction appears relative to total reports for capivasertib.
These are voluntary reports and do not establish that capivasertib caused these reactions.
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Other drugs that appear in adverse event reports alongside capivasertib. 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.
89.2% of capivasertib adverse event reports involve female patients and 2.4% involve male patients. The largest age group is elderly at 56%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking capivasertib when the adverse event was reported.
Showing 15 of 69 indications
Capivasertib is sold under the brand name Truqap.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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