20 to 50     : Dose as in normal renal function
10 to 20     : Dose as in normal renal function
<10           : Dose as in normal renal function
DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES
CAPD                :Not dialysed. Dose as in normal renal function
HD                     :Not dialysed. Dose as in normal renal function
HDF/high flux   :Unknown dialysability. Dose as in normal renal function
CAV/VVHD      :Not dialysed. Dose as in normal renal function
IMPORTANT DRUG INTERACTIONS
Potentially hazardous interactions with other drugs
Analgesics: increased risk of nephrotoxicity with NSAIDs; antagonism of diuretic effect with NSAIDs
Anti-arrhythmics: risk of cardiac toxicity with anti-arrhythmics if hypokalaemia occurs; effects of lidocaine and mexiletine antagonised
Antibacterials: increased risk of ototoxicity with aminoglycosides, polymyxins and vancomycin; avoid concomitant use with lymecycline
Antidepressants: increased risk of hypokalaemia with reboxetine; enhanced hypotensive effect with MAOIs; increased risk of postural hypotension with tricyclics
Anti-epileptics: increased risk of hyponatraemia with carbamazepine
Antifungals: increased risk of hypokalaemia with amphotericin
Antihypertensives: enhanced hypotensive effect; increased risk of first dose hypotensive effect with alpha-blockers; increased risk of ventricular arrhythmias with sotalol if hypokalaemia occurs
Antipsychotics: increased risk of ventricular arrhythmias with amisulpride, sertindole or pimozide if hypokalaemia occurs – avoid with pimozide; enhanced hypotensive effect with phenothiazines
Atomoxetine: increased risk of ventricular arrhythmias if hypokalaemia occurs
Cardiac glycosides: increased toxicity if hypokalaemia occurs
Lithium: risk of toxicity
ADMINISTRATION
Reconstition
–
Route
Oral, IV, IM
Rate of Administration
IV infusion
: 2–5 mg in 500 mL of infusion fluid over 30–60 minutesIV bolus: 1–2 mg over 3–4 minutes
Comments
Compatible with glucose 5% or sodium chloride 0.9%
OTHER INFORMATION
1 mg bumetanide ≡ 40 mg furosemide at low doses, but avoid direct substitution at high doses
In patients with severe chronic renal failure given high doses of bumetanide there are reports of musculoskeletal pain and muscle spasm
Orally: diuresis begins within 30 minutes, peaks after 1–2 hours, lasts 3 hours
IV: diuresis begins within few minutes and ceases in about 2 hours
Use with caution in patients receiving nephrotoxic or ototoxic drugs
Smaller doses may be sufficient in the elderly and cirrhotics (500 micrograms)