The most commonly reported side effects of terlipressin include electrocardiogram qt prolonged, renal impairment, and ascites, based on 303 FDA adverse event reports from 2004 to 2025. 11.9% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for terlipressin.
These are voluntary reports and do not establish that terlipressin caused these reactions.
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Other drugs that appear in adverse event reports alongside terlipressin. 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.
31.4% of terlipressin adverse event reports involve female patients and 56.4% involve male patients. The largest age group is adult at 64%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking terlipressin when the adverse event was reported.
Showing 15 of 57 indications
Terlipressin is sold under the brand name Terlivaz.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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