Clinical and pharmacological group: & nbsp

Vaccines, serums, phages and toxoids

Included in the formulation
  • Tularemia live vaccine
    lyophilizate in / skin cutaneous 
  • АТХ:

    J.07.A.X   Other vaccines for the prevention of bacterial infections

    Pharmacodynamics:

    Stimulates the appearance of antibodies to the causative agent of tularemia 20-30 days after administration, provides immunity to tularemia for 5 years.

    Pharmacokinetics:

    Not described.

    Indications:

    It is used to prevent tularemia in a planned manner or according to epidemic indications.

    XXI.Z20-Z29.Z23.4   The need for immunization against tularemia

    Contraindications:

    Acute infectious and non-infectious diseases, chronic diseases in the acute stage - vaccinations are given no earlier than 1 month after recovery or remission, pregnancy and lactation, age up to 3 years, individual intolerance.

    Carefully:

    History of hypersensitivity to the introduction of vaccines.

    Pregnancy and lactation:

    Recommendations for FDA - Category C. Contraindicated during pregnancy and lactation.

    Dosing and Administration:

    Nasojno or intradermally, it is single. Revaccination is carried out after 5 years.

    The highest daily dose: with dermal administration - 0.1 ml (200 million microbial bodies); with intradermal administration - 0.1 ml (50 million microbial bodies).

    The highest single dose: with dermal administration - 0.1 ml (200 million microbial bodies); with intradermal administration - 0.1 ml (50 million microbial bodies).

    Side effects:

    Local manifestations: hyperemia, tenderness at the injection site.

    Common reactions: rarely - hyperthermia. Headache.

    Allergic reactions.

    Overdose:

    Cases of overdose not described.

    Treatment is symptomatic.

    Interaction:

    Clinically significant interactions are not described.

    Special instructions:

    On the procedure for the administration of the drug is noted in a special journal indicating the date of the procedure, the name of the drug, the serial number, the manufacturer's company and the response to the inoculation.

    Instructions
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