The most commonly reported side effects of taurolidine include vascular device infection, vomiting, and abdominal pain, based on 161 FDA adverse event reports from 2009 to 2025.
Percentages show how often each reaction appears relative to total reports for taurolidine.
These are voluntary reports and do not establish that taurolidine caused these reactions.
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Other drugs that appear in adverse event reports alongside taurolidine. 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.
64.0% of taurolidine adverse event reports involve female patients and 29.8% involve male patients. The largest age group is adult at 49%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking taurolidine when the adverse event was reported.
Showing 15 of 32 indications
Taurolidine is sold under the brand name Defencath.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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