The most commonly reported side effects of digoxin include dyspnoea, fatigue, and nausea, based on 75,361 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for digoxin.
These are voluntary reports and do not establish that digoxin caused these reactions.
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Other drugs that appear in adverse event reports alongside digoxin. 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.
50.3% of digoxin adverse event reports involve female patients and 44.1% involve male patients. The largest age group is elderly at 72%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking digoxin when the adverse event was reported.
Showing 15 of 633 indications
Digoxin is sold under the brand name Lanoxicaps.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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