Bumetanide
Brand names: Burinex
Bumetanide is a loop diuretic used for oedema and for fluid overload in heart failure.
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.
US labelling (FDA)
Reference — US labelling, may differ from UKDOSAGE AND ADMINISTRATION Individualize dosage with careful monitoring of patient response. Oral Administration The usual total daily dosage of bumetanide tablets is 0.5 mg to 2 mg and in most patients is given as a single dose. If the diuretic response to an initial dose of bumetanide tablets is not adequate, in view of its rapid onset and short duration of action, a second or third dose may be given at 4- to 5- hour intervals up to a maximum daily dose of 10 mg. An intermittent dose schedule, whereby bumetanide tablets are given on alternate days or for 3 to 4 days with rest periods of 1 to 2 days in between, is recommended as the safest and most effective method for the continued control …
Source: US FDA prescribing information (openFDA / DailyMed), label dated 2025-01-08. Accessed 2026-06-12. US dosing and indications can differ from UK practice — use UK sources for prescribing decisions.
Clinical monograph
How it works
It inhibits the sodium-potassium-chloride co-transporter in the ascending loop of Henle, producing a brisk diuresis with loss of sodium, potassium and water.
Prescribing in practice
- Monitor U&E for hypokalaemia, hyponatraemia and dehydration, which can be marked with vigorous diuresis.
- It is more reliably absorbed orally than furosemide, making it useful where gut-wall oedema impairs furosemide absorption.
- Gout can be precipitated, and ototoxicity is a risk with high intravenous doses or rapid administration, particularly in renal impairment.
Monitoring
Monitor renal function, electrolytes (especially potassium and sodium) and fluid/volume status, with closer review during dose titration or intercurrent illness.
Counselling the patient
- Expect increased passing of urine; take earlier in the day to avoid disturbed sleep.
- Report muscle cramps, marked weakness, dizziness on standing or significant thirst, which may indicate salt or fluid imbalance.
Evidence & guidelines
Established loop diuretic for oedema and heart failure (NICE NG106).
Reference: ESC Heart Failure Guidelines 2021; 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.
- Hyperkalaemia Management · UK Kidney Association Guidelines 2020; NICE CKD Guidelines
- Rhabdomyolysis · Renal Association 2018; UpToDate 2024
- Hypocalcaemia (Adult) · Society for Endocrinology
- SIADH (Endocrine Perspective) · European Hyponatraemia Guidelines 2014
- Hepatorenal Syndrome · EASL 2018; ICA 2015
- Acute Kidney Injury (AKI) · KDIGO 2012 / NICE AKI 2019