This site is intended for UK healthcare professionals
Medscape UK Univadis Logo
Medscape UK Univadis Logo

Typhoid vaccine oral

Updated 2 Feb 2023 | Typhoid vaccine

Presentation

Oral vaccine containing Salmonella enterica serovar Typhi Ty21a

Drugs List

  • typhoid oral vaccine gastro-resistant capsules
  • VIVOTIF gastro-resistant capsules
  • Therapeutic Indications

    Uses

    Vaccination against typhoid fever

    Active oral immunisation against typhoid fever.

    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

    Dosage

    Adults

    One capsule to be taken on day 1. The second capsule should be taken on day 3 and the third capsule on day 5.

    The vaccine schedule should be completed at least 1 week before the risk of exposure to typhoid fever.

    Revaccination
    In patients who remain at risk of exposure to typhoid fever, revaccination comprises the ingestion of three capsules on days 1, 3 and 5.

    Children

    Children aged 5 years and above
    One capsule to be taken on day 1. The second capsule should be taken on day 3 and the third capsule on day 5.

    The vaccine schedule should be completed at least 1 week before the risk of exposure to typhoid fever.

    Revaccination
    In patients who remain at risk of exposure to typhoid fever, revaccination comprises the ingestion of three capsules on days 1, 3 and 5.

    Additional Dosage Information

    The vaccine contains live Salmonella and a course of treatment should not be started until 3 days after completion of any antibacterial therapy; it is also preferred that antibacterial therapy is not started until 3 days after completion of the vaccine course of treatment.

    If concurrent malaria prophylaxis is required, there should be an interval of at least 3 days between completion of the course of vaccine and the first dose of malaria prophylaxis, except that the fixed dose combination of proguanil and atovaquone may be used concurrently, as may mefloquine, provided that for mefloquine the dose is taken at least 12 hours after the vaccine dose.

    Contraindications

    Children under 5 years
    Febrile disorder
    Immunosuppression
    Breastfeeding
    Galactosaemia
    Gastrointestinal disorder
    Hereditary fructose intolerance
    Immunodeficiency syndromes
    Pregnancy

    Precautions and Warnings

    Glucose-galactose malabsorption syndrome
    Lactose intolerance

    Live vaccine must not be given during/within 6 months of chemotherapy
    Live vaccine must not be given during/within 6 months of radiotherapy
    Postpone immunisation if there is active or suspected infection
    Advise ability to drive/operate machinery may be affected by side effects
    Previous/Concurrent medicine consider washout period: See prescribing info
    Vaccine may not be effective in 100% of patients
    Contains lactose
    Preparation contains sucrose
    Follow national immunisation guidelines
    Advise patient on timing of malaria prophylaxis if required concurrently

    Unless the immunisation schedule of 3 vaccine capsules is completed, an optimal immune response may not be achieved.

    Even after three doses, not all recipients of typhoid oral vaccine will be fully protected against typhoid fever. Therefore, travellers should take all necessary precautions to avoid contact with or ingestion of potentially contaminated food or water.

    Protection against typhoid fever commences approximately 7 to 10 days after ingesting the third dose of vaccine.

    Under conditions of repeated or continuous exposure to S. typhi protection persists for at least 3 years. In the case of travel from a non-endemic area to an area where typhoid fever is endemic, a booster consisting of three doses is recommended every 3 years.

    Pregnancy and Lactation

    Pregnancy

    Typhoid oral vaccine is contraindicated during pregnancy.

    The manufacturer states that typhoid oral vaccine should not be administered during pregnancy unless it is clearly needed when there is an increased risk of infection. At the time of writing there is limited published information regarding the use of the live oral typhoid vaccine during pregnancy. Potential risks are unknown. The Green book suggests that this vaccine should only be considered if there is no alternative vaccine.

    Lactation

    Typhoid oral vaccine is contraindicated during breastfeeding.

    The manufacturer does not recommend using typhoid oral vaccine during breastfeeding. It is not known if typhoid oral vaccine is excreted in human milk. There is also no data available regarding the extent the inactive ingredient dibutyl phthalate (DBP) may be excreted with breast milk. Effects on exposed infants are unknown.

    Side Effects

    Abdominal distension
    Abdominal pain
    Anaphylactic reaction
    Arthralgia
    Asthenia
    Back pain
    Chills
    Decreased appetite
    Dermatitis
    Diarrhoea
    Dizziness
    Fatigue
    Fever
    Flatulence
    Headache
    Hypersensitivity reactions
    Influenza-like symptoms
    Malaise
    Myalgia
    Nausea
    Paraesthesia
    Pruritus
    Rash
    Shock
    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: January 2020

    Reference Sources

    Drugs During Pregnancy and Lactation: Treatment Options and Risk Assessment, 3rd edition (2015) ed. Schaefer, C., Peters, P. and Miller, R. Elsevier, London.

    Drugs in Pregnancy and Lactation: A Reference Guide to Fetal and Neonatal Risk, 10th edition (2015) ed. Briggs, G., Freeman, R. Wolters Kluwer Health, Philadelphia.

    Summary of Product Characteristics: Vivotif Gastro-resistant capsules, hard. PaxVax Ltd. Revised July 2018.

    Immunisation against infectious disease - The Green Book.
    Available at https://www.gov.uk/government/collections/immunisation-against-infectious-disease-the-green-book
    Last accessed: 21 January 2020.

    NICE Evidence Services Available at: www.nice.org.uk Last accessed: 21 January 2020

    Access the full UK drug database with a FREE Medscape UK Account
    It takes just a few minutes, and you’ll get unlimited access to information on over 11,000 UK drugs.
    Register for Free

    Already a member? Log in

    Medscape UK | Univadis prescription drug monographs & interactions are based on FDB Multilex Content

    FDB Logo

    FDB Disclaimer : FDB Multilex is intended for the use of healthcare professionals and is provided on the basis that the healthcare professionals will retain FULL and SOLE responsibility for deciding what treatment to prescribe or dispense for any particular patient or circumstance.