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Shingles (herpes zoster) recombinant adjuvant virus antigen vaccine

Presentation

Vaccine containing recombinant, adjuvanted varicella zoster virus glycoprotein E antigen.

For comprehensive information or advice on this product or the immunisation programme in the UK, the following website should be accessed.

https://www.gov.uk/government/collections/immunisation-against-infectious-disease-the-green-book

Drugs List

  • shingles (herpes zoster) recombinant adjuvanted vaccine
  • SHINGRIX vaccine vial
  • Therapeutic Indications

    Uses

    Herpes zoster (shingles): prevention
    Herpes zoster related post herpatic neuralgia: prevention

    Dosage

    Adults

    Adults aged 50 years old and older
    Initial dose of 0.5ml.
    Additional 0.5ml dose to be administered 2 to 6 months after initial dose. Alternatively, in patients who are or may become immunodeficient or immunosuppressed, the second dose may be administered 1 to 2 months after the initial dose.

    Adults aged 18 years old and older at an increased risk of herpes zoster
    Initial dose of 0.5ml.
    Additional 0.5ml dose to be administered 2 to 6 months after initial dose. Alternatively, in patients who are or may become immunodeficient or immunosuppressed, the second dose may be administered 1 to 2 months after the initial dose.

    Administration

    To be administered by intramuscular injection only, preferably into the deltoid muscle.

    Contraindications

    Children under 18 years
    Febrile disorder
    Pregnancy

    Precautions and Warnings

    History of herpes zoster infection
    Immunosuppression
    Patients under 50 years
    Breastfeeding
    Coagulopathy
    Immunodeficiency syndromes
    Thrombocytopenia

    Postpone immunisation if there is active or suspected infection
    Advise ability to drive/operate machinery may be affected by side effects
    Impaired response possible in immunocompromised patients
    Vaccine may not be effective in 100% of patients
    Contains polysorbate
    Inject other vaccines at different sites
    Record name and batch number of administered product
    Resuscitation facilities must be immediately available
    Risk of Guillain-Barre syndrome may be increased
    Follow national immunisation guidelines

    Pregnancy and Lactation

    Pregnancy

    The shingles (herpes zoster) virus antigen vaccine is contraindicated during pregnancy.

    The manufacturer recommends as a precautionary measure to avoid the use of shingles (herpes zoster) virus antigen vaccine during pregnancy. At the time of writing, limited published information is available regarding the use of the shingles (herpes zoster) virus antigen vaccine during pregnancy.

    Lactation

    Use the shingles (herpes zoster) virus antigen vaccine with caution during breastfeeding.

    The manufacturer does not make any recommendations regarding the use of the shingles (herpes zoster) virus antigen vaccine during breastfeeding. The effect of the shingles (herpes zoster) virus antigen vaccine on breastfeeding has not been studied. It is unknown if the shingles (herpes zoster) virus antigen vaccine is excreted into breast milk.

    Side Effects

    Abdominal pain
    Angioedema
    Arthralgia
    Chills
    Diarrhoea
    Fatigue
    Headache
    Injection site reactions
    Lymphadenopathy
    Malaise
    Myalgia
    Nausea
    Pain / soreness (injection site)
    Pruritus
    Pyrexia
    Rash
    Swelling (injection site)
    Urticaria
    Vomiting

    Overdosage

    It is strongly recommended that the UK National Poisons Information Service be consulted on cases of suspected or actual overdose where there is doubt over the degree of risk or about appropriate management.

    The following number will direct the caller to the relevant local centre (0844) 892 0111

    Information may be obtained if you have access to ToxBase the primary clinical toxicology database of the National Poisons Information Service. This is available via password on the internet ( www.toxbase.org ) or if this is unavailable at the backup site ( www.toxbasebackup.org ).

    Further Information

    Last Full Review Date: November 2022

    Reference Sources

    Summary of Product Characteristics: Shingrix powder and suspension for suspension for injection. GlaxoSmithKline Ltd. Revised June 2022.

    NICE Evidence Services Available at: www.nice.org.uk Last accessed: 07 November 2022.

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