The most commonly reported side effects of triheptanoin include vomiting, diarrhoea, and rhabdomyolysis, based on 515 FDA adverse event reports from 2020 to 2025.
Percentages show how often each reaction appears relative to total reports for triheptanoin.
These are voluntary reports and do not establish that triheptanoin caused these reactions.
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Other drugs that appear in adverse event reports alongside triheptanoin. 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.
44.5% of triheptanoin adverse event reports involve female patients and 47.2% involve male patients. The largest age group is child at 40%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking triheptanoin when the adverse event was reported.
Showing 15 of 42 indications
Triheptanoin is sold under the brand name Dojolvi.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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