The most commonly reported side effects of dicumarol include chest pain, rib fracture, and upper respiratory tract infection, based on 67 FDA adverse event reports from 2004 to 2024.
Percentages show how often each reaction appears relative to total reports for dicumarol.
These are voluntary reports and do not establish that dicumarol caused these reactions.
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Other drugs that appear in adverse event reports alongside dicumarol. 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.
65.7% of dicumarol adverse event reports involve female patients and 28.4% involve male patients. The largest age group is adult at 69%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking dicumarol when the adverse event was reported.
Dicumarol is sold under the brand name Dicumarol.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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