Frusemide (Lasix/Urex)

  • Description and indication for use

    Frusemide is a potent diuretic with a rapid onset of action.  The onset after IV administration is within 5 to 20 minutes with peak diuresis between 1 to 3 hours.  Duration of action is between 4 to 6 hours.

    It can be used to treat acute episodes of fluid overload as sometimes seen in infants with chronic lung disease or associated with oliguria.  Can be used to treat other fluid/electrolyte disturbances.

    We do not routinely give Frusemide in association with top-up transfusions in infants receiving transfusions.

    Please note:  Frusemide may cause deafness.  This is more likely to occur when there are high peak concentrations of the drug, as occurs with bolus intravenous administration, or very large oral doses. See, for example, Laryngoscope 1985; 95(9 Pt 2 Suppl 38): 1-4, J Otolaryngology 1982; 11:127-133, Klinische Wochenschrift 1970; 48:1052-1056.

    Dose

    IV & O:

    0.5 to 2 mg/kg/dose (higher doses may occasionally be used).

    VLBW Daily
    Term  
         Week 1 daily
         Week 2 and over 12 hourly

    Continuous 24 hour IV infusion: 

    0.1 – 1 mg/kg/hr.

    Dose may be increased in resistant cases and in renal impairment.

    Anuric/oliguric renal failure may require doses of 3 mg/kg or higher to establish urine output.

    Reconstitution/Dilution

    Ampoule = 20 mg in 2 mL.

    IV:

    Withdraw required dose further dilute so that the dose can be administered over the appropriate time frame.

    IV administration is recommended. 

    Give IM when no IV access is available.

    IM:

    No dilution is necessary.

    IV Infusion

    DRUG HOW TO MAKE UP DOSE EQUIVALENT DOSE RANGE
    Frusemide 10 mg/kg in 50 mL 1 mL/hr = 0.2 mg/kg/hour 0.1 to 1 mg/kg/hour
    50 mg/kg in 50 mL 1 mL/hr = 1 mg/kg/hour

    Route and method of administration

    IV:

    Never give Frusemide as a bolus intravenously. 

    Administer intravenous doses at a maximum rate of 0.05 mg/kg/min – for example, a 1.0 mg/kg dose should be infused over at least 20 minutes.

    Whenever possible, give high doses by continuous intravenous infusion (because of drug incompatibilities, this will often require another IV cannula to be inserted). 

    If being given in association with top-up transfusion, dose should be given half way through transfusion.

    Side effects

    Hypokalaemia.

    Electrolyte and fluid disturbances.

    Hypercalciuiria and development of renal calculi (long term therapy).

    Hyperglycaemia, glycosuria.

    Dehydration, hypovolaemia, hypotension.

    Thrombophlebitis at injection site.

    Hypochloraemic metabolic alkalosis.

    Chronic therapy may cause nephrocalcinosis and osteopenia with potential for rickets and fractures.

    Risk of ototoxicity is increased with renal impairment, high doses, rapid IV administration and use of other ototoxic drugs.

    Compatible Solutions

    Sodium Chloride 0.9%.

    Glucose 5%.

    Incompatibilities

    Administer alone, or contact pharmacy for further information if required.

    Check compatibilities with other intravenous fluids when mixing is unavoidable.  For example, Frusemide is not compatible with Amphotericin (in saline), Ampicillin, Amrinone, Atracurium, Benztropine, Chlorpromazine, Cimetidine, Cotrimoxazole, Diazepam, Dobutamine, Esmolol, Fentanyl, Gentamicin (in Glucose) Isoprenaline, Magnesium, Metaraminol, Midazolam, Noradrenaline, Ondansetron, Phentolamine, Phenytoin, Prochlorperazine, Promethazine, Protamine, Vancomycin or Verapamil.

    Special precautions

    CAUTION in patients with renal failure.

    CAUTION in patients with acidosis, low serum albumin, hyperbilirubinaemia or jaundice.

    If used long term, monitor potassium and consider potassium supplementation or the addition of a potassium-sparing diuretic.

    Administration of oral Frusemide – divide doses as much as possible throughout the day (i.e. 2 – 3 small doses instead of a single, large daily dose).

Disclaimer:  This Drug information was designed for use by PIPER Neonatal. Whilst great care has been taken to check the information is accurate, it is possible that errors may have been missed. Furthermore, dosage schedules are continually being revised and new side effects recognised. For these reasons, the reader is strongly advised to consult the drug companies' printed information before administering any of the drugs recommended in this book.
Most drugs in this document are appropriate only for specialist use in hospitals.  A number of drugs should only be used in consultation with the appropriate Paediatric subspecialist. 

Note: The electronic version of this guideline is the version currently in use.  Any printed version cannot be assumed to be current. Printed copies of this document are valid for