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Terlipressin Intravenous for Adults

Who can administer

May be administered by registered competent doctor or nurse/midwife

Important information

Available preparations

Terlipressin 1mg per 5ml vial (EVER Pharma)

Glypressin 1mg in 8.5mL ampoule (not routinely stocked in GUH)

Reconstitution

Terlipressin 1mg per 5ml vial (EVER Pharma)

  • Already in solution

Glypressin

  • Already in solution
  • Draw up using a 5 micron filter needle

Infusion fluids

Not generally required- product ready for use

  • but see under Further Information regarding use as a continuous intravenous infusion

Methods of intravenous administration

Bolus intravenous injection

  • Administer required dose over at least 1 minute (ref 1)

Continuous intravenous infusion (Hepato-Renal Syndrome (HRS) only)

  • Not commonly used in GUH to date
  • May be considered to reduce risk of some adverse effects - see guidance here
  • See under Further Information

    Dose in adults

    Short term management of bleeding oesophageal varices (SPC and ref 2)

    • Different preparations of terlipressin are available (Terlipressin EVER Pharma, Glypressin) -these have different indications and are licensed at different doses for the same indication.
    • Hence, clinical judgement is required when prescribing
    Weight Dose Duration

    Terlipressin

    (Ever pharma)

    <50kg Initially 1mg, then 1mg every 4 to 6 hours 48 to 72 hours
    50 to 70kg Initially 1.5mg, then 1mg every 4 to 6 hours
    70kg or more Initially 2mg, then 1mg every 4 to 6 hours

    Glypressin

    <50kg Initially, 2mg every four hours until bleeding controlled, then reduced to 1mg every four hours, if required maximum of 48 hours
    >50kg Initially, 2mg every four hours until bleeding controlled, reduced if not tolerated to 1mg every four hours
    Type 1 Hepato-renal syndrome (HRS)
    • Dose below is as per BNF - the doses in the product SPCs can differ from this
    • Hence, clinical judgement is required when prescribing
    Dose Duration Comment

    Give 1mg every 4 to 6 hours, increased if necessary up to 2mg every four hours

    Dose to be increased if serum creatinine does not decrease by at least 25% after 3 days

    Usual total duration of treatment: 7 days (up to a max of 14 days)

    Discontinue treatment when serum creatinine falls below 133 micromol/L

    Note new safety concerns with the use of this drug in HRS

    Renal impairment

    • Hepatorenal syndrome

      • Avoid in advanced renal dysfunction i.e.baseline serum creatinine >442 micromol/L unless the benefit is judged to outweigh the risk
      • See also new safety warnings - see guidance here

    Hepatic impairment

    • Hepatorenal syndrome

      • Avoid in severe liver disease defined as Acute-on-Chronic Liver failure (ACLF) grade 3 and/or MELD score 39 or more unless the benefit is judged to outweigh the risk
      • See also new safety warnings - see guidance here

    Monitoring

    • Monitor blood pressure, heart rate, haematology, fluid balance and electrolytes
    • HRS: respiratory adverse effects have been reported - see new safety guidance here

    Further information

    Continuous intravenous infusion (HRS only)

    • Not commonly used in GUH to date
    • Suggested as an option to reduce risk of some adverse effects - see guidance here
    • Dilution options (ref 1)
      • Using 1mg in 50mL Glucose 5% (20 micrograms/mL)
      • Using 2mg in 100mL Glucose 5% (20 micrograms/mL)
      • Using 5mg in 250mL Glucose 5% (20 micrograms/mL)
    • Dose (HRS)
      • Starting dose 2mg over 24 hours
      • Increased to a maximum of 12mg over 24 hours
      • Adjust dose according to response

    Storage

    • Store between 2 to 80C
    • Do not freeze

    References

    Terlipressin 1mg per 5ml via (EVER Pharma) March 2025

    Glypressin SPC March 2023

    1. Injectable Medicines Administration Guide downloaded from Medusa 20th March 2025

    2. BNF accessed online via medicinescomplete 19/06/2025

    Therapeutic classification

    Posterior pituitary hormone

    IV Guide Type