Digoxin
Brand names: Lanoxin
Digoxin is a cardiac glycoside used for rate control in atrial fibrillation and in heart failure; in older people its narrow therapeutic index and reliance on renal clearance make toxicity a key concern.
ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.
Clinical monograph
How it works
It inhibits the myocardial sodium-potassium ATPase, raising intracellular calcium to increase contractility, and enhances vagal tone to slow atrioventricular conduction.
Prescribing in practice
- Older patients are highly susceptible to toxicity because of declining renal function and low body mass, so use lower doses, account for renal impairment, and recognise that hypokalaemia, hypomagnesaemia and hypercalcaemia potentiate toxicity.
- Many interacting drugs (including amiodarone, verapamil, diuretics and macrolides) raise levels or precipitate toxicity, so review co-prescriptions carefully.
- Toxicity may present atypically as confusion, nausea, anorexia, visual disturbance or new arrhythmia.
Monitoring
Monitor renal function and electrolytes (particularly potassium), heart rate and clinical response, with digoxin level measurement guided by symptoms and taken at an appropriate interval after dosing.
Counselling the patient
- Report nausea, loss of appetite, confusion, visual changes or palpitations, which can signal toxicity.
- Do not stop or change the dose without advice, and keep regular blood tests.
- Tell clinicians about all new medicines, as many interact with digoxin.
Evidence & guidelines
Long-standing trial and registry data support digoxin for rate control and symptom relief, while pharmacokinetic principles underpin cautious dosing and monitoring in older patients with reduced renal reserve.
Reference: NICE NG106 (Chronic Heart Failure); ESC AF Guidelines 2020; STOPP/START v3; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- Falls Assessment in Older Adults · NICE CG161 2013
- Delirium Outside ICU · NICE CG103
- Comprehensive Geriatric Assessment (CGA) · BGS / NICE
- Delirium Assessment and Management · NICE CG103 2010
- Frailty Recognition and Management · BGS Frailty Framework / NHS NHSE
- Polypharmacy and Medicines Optimisation · STOPP/START v2 2014 / NICE NG5