The most commonly reported side effects of lomitapide include diarrhoea, weight decreased, and therapy cessation, based on 4,001 FDA adverse event reports from 2013 to 2025.
Percentages show how often each reaction appears relative to total reports for lomitapide.
These are voluntary reports and do not establish that lomitapide caused these reactions.
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Other drugs that appear in adverse event reports alongside lomitapide. 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.
49.5% of lomitapide adverse event reports involve female patients and 27.2% involve male patients. The largest age group is adult at 67%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking lomitapide when the adverse event was reported.
Showing 15 of 47 indications
Lomitapide is sold under the brand name Juxtapid.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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