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CARDIOVASCULAR SYSTEM › CARDIAC THERAPY › CARDIAC GLYCOSIDES › Digitalis glycosides
digoxin
C01AA05
Forms & Strengths
- Oral tablets: 62.5 mcg, 125 mcg, 250 mcg
- Oral solution: 50 mcg/mL
- Injection: 250 mcg/mL
Adult Dosing
- Heart failure: 125 to 250 mcg orally once daily
- Atrial fibrillation (rate control): 0.125 to 0.25 mg orally once daily
- Digitalization (rapid): 0.5 to 1 mg given in divided doses over 24 hours
Pediatric Dosing
- Neonates/Infants/Children: Dosing varies significantly by age and indication; consult specialized pediatric literature and calculate based on lean body weight
- Maintenance: Typically 8 to 10 mcg/kg/day divided every 12 hours orally for children 2-5 years
Indications
- Heart failure with reduced ejection fraction (HFrEF)
- Atrial fibrillation (rate control)
Mechanism of Action
- Inhibition of the Na+/K+-ATPase membrane pump in myocardial cells
- Increases intracellular sodium, leading to increased intracellular calcium via the Na+/Ca2+ exchanger
- Enhances myocardial contractility (positive inotrope)
- Decreases conduction through the AV node via parasympathetic and sympathetic modulation
Contraindications
- Ventricular fibrillation
- Ventricular tachycardia
- Hypersensitivity to digoxin
- Second- or third-degree heart block (unless a functioning artificial pacemaker is present)
- Wolff-Parkinson-White syndrome with pre-excitation
Adverse Reactions
- Nausea, vomiting, diarrhea, anorexia
- Visual disturbances (blurred vision, yellow-green halos)
- Cardiac arrhythmias (bradycardia, heart block, ventricular tachycardia)
- Dizziness, confusion, fatigue
Drug Interactions
- P-glycoprotein inhibitors (e.g., amiodarone, verapamil, dronedarone) increase digoxin concentrations
- Loop and thiazide diuretics cause hypokalemia and hypomagnesemia, increasing toxicity risk
- Beta-blockers and non-dihydropyridine calcium channel blockers increase risk of bradycardia and AV block
- Indducers of P-gp/CYP (e.g., rifampin, St. John's wort) decrease digoxin concentrations
Curated Content: Needs Vetting Before Put to Clinical Use