The most commonly reported side effects of levopropoxyphene include chronic kidney disease, renal failure, and acute kidney injury, based on 110 FDA adverse event reports from 2004 to 2023. 5.5% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for levopropoxyphene.
These are voluntary reports and do not establish that levopropoxyphene caused these reactions.
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Other drugs that appear in adverse event reports alongside levopropoxyphene. 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.
71.8% of levopropoxyphene adverse event reports involve female patients and 27.3% involve male patients. The largest age group is adult at 57%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking levopropoxyphene when the adverse event was reported.
Levopropoxyphene is sold under the brand name Novrad.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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