| Drug Overview | |
|---|---|
| Drug Class | Cardiac Glycoside |
| Subclass | Na⁺/K⁺ ATPase Inhibitor |
| Primary Uses | HFrEF; Atrial Fibrillation |
| Route | Oral / IV |
| Onset (IV) | 5–30 minutes |
| Half-life | ~36–48 hours (normal renal function) |
| Metabolism | Minimal hepatic |
| Elimination | Renal |
| Renal Adjustment | Yes |
| Hepatic Adjustment | No |
| Therapeutic Level | 0.5–0.9 ng/mL (HF) |
| Black Box Warning | No |
Digoxin is a cardiac glycoside that increases inotropy and enhances vagal tone.
It is used in:
It is NOT first-line therapy in modern heart failure but remains useful in select patients.
Primary Target:
Cellular Effect:
Result:
Autonomic Effect:
Net Effects:
Cardiovascular:
Not used for:
See also:
Heart Failure (maintenance):
Atrial Fibrillation:
Renal dosing:
Target serum concentration:
Absolute:
Relative:
Common:
Cardiac:
Visual:
Toxicity Risk Increases With:
Mechanism:
ECG Findings:
Treatment:
See:
Increase Digoxin Levels:
Electrolyte-mediated Risk:
Additive AV Nodal Suppression:
Monitor especially in:
Unlike:
Digoxin: