The most commonly reported side effects of phenprocoumon include general physical health deterioration, dyspnoea, and anaemia, based on 2,801 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for phenprocoumon.
These are voluntary reports and do not establish that phenprocoumon caused these reactions.
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Other drugs that appear in adverse event reports alongside phenprocoumon. 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.
43.6% of phenprocoumon adverse event reports involve female patients and 49.9% involve male patients. The largest age group is elderly at 78%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking phenprocoumon when the adverse event was reported.
Showing 15 of 118 indications
Phenprocoumon is sold under the brand name Liquamar.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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