The most commonly reported side effects of conivaptan include blood sodium increased, atrial fibrillation, and death, based on 54 FDA adverse event reports from 2006 to 2024. 13.0% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for conivaptan.
These are voluntary reports and do not establish that conivaptan caused these reactions.
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Other drugs that appear in adverse event reports alongside conivaptan. 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.
46.3% of conivaptan adverse event reports involve female patients and 38.9% involve male patients. The largest age group is elderly at 50%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking conivaptan when the adverse event was reported.
Conivaptan is sold under the brand name Vaprisol.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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