• Presentation
  • Dose adjustment
  • Maximum dose 60 mg/kg/day Total cumulative dose
  • Administration
  • Neonatal Intensive Care Drug Manual




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    Drug type

    Non-narcotic analgesic and antipyretic.

    Trade name

    Intravenous: Paracetamol Actavis; Paracetamol ACT; Paracetamol BNM; Paracetamol IV Pfizer; Paracetamol Kabi; Paracetamol-AFT; Paramat

    Oral: Dymadon, Febridol, Panadol (Children)



    Presentation

    IV: 500 mg/50 mL, 1000 mg/100 mL (10 mg/mL) vial or infusion bag

    Oral: 100 mg/mL drops



    Dose

    Analgesia/Antipyretic/Adjunct to post-operative analgesia

    Oral/Intravenous/Rectal1-3:



    Weight*

    Loading

    Maintenance

    <2.0 kg

    15 mg/kg

    7.5 mg/kg every 6 hours

    2.0 – 3.0 kg

    15 mg/kg

    10 mg/kg every 6 hours

    >3.0 kg

    20 mg/kg

    10 mg/kg every 6 hours

    *Current/best weight
    Patent Ductus Arteriosus (treatment course 3-7 days with 48-hourly monitoring of liver function)

    Oral/Intravenous4,5:



    Criteria

    Loading

    Maintenance

    ≥28 weeks CGA/PMA and ≥1000 g*

    15 mg/kg

    15 mg/kg every 6 hours

    <28 weeks and/or <1000 g**

    15 mg/kg

    7.5 mg/kg every 6 hours**

    *Current/best weight

    **Higher maintenance doses (15 mg/kg) in extreme preterm infants have been used but there are limited safety data. At Canberra Hospital, a dose of 15mg/kg 6 hourly is used for treatment in all patients



    Dose adjustment


    Therapeutic hypothermia –Caution to be applied with associated hepatic and renal impairment.

    Renal impairment – Refer to precautions section.

    Hepatic impairment – Refer to monitoring and precautions sections.


    Maximum dose

    60 mg/kg/day

    Total cumulative dose




    Route

    IV, oral, rectal

    Preparation

    Intravenous: Use undiluted. Can be diluted to 2 mg/ml for use in ELBW infants using sodium chloride 0.9% or glucose 5%. If diluted, the solution should be used immediately.

    Administration

    Intravenous:

    Administer over 15 minutes via syringe driver.

    Oral:

    Can be given with or without feeds. Shake bottle well before measuring dose.



    Rectal:

    Dilute oral mixture 1:1 with water for rectal doses. Low dose suppositories are not commercially available but can be prepared by selected pharmacy departments. Do not cut suppositories to make part rectal dose.



    Monitoring

    Monitor hepatic and renal function.

    If signs of acute liver injury (example, raised ALT >50 IU/L) – refer to acetylcysteine formulary and contact Poisons Information Centre (13 11 26 for New South Wales) or local toxicology service.




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    Neonatal Intensive Care Drug Manual

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