Clinical and pharmacological group: & nbsp

Antiviral drugs (excluding HIV)

Included in the formulation
  • Relenza®
    powder d / inhal. 
  • АТХ:

    J.05.A.H.01   Zanamivir

    Pharmacodynamics:

    An antiviral agent. Selectively inhibits neuraminidase, the surface enzyme of the influenza virus. It disrupts the replication of influenza A and B viruses, neutralizes all known subtypes of influenza A neuraminidase. Inhibits the release of viruses from the epithelial cells of the respiratory tract.

    Pharmacokinetics:

    Means for topical application. With inhalation, absorption is low, systemic effects on the body do not.

    Indications:

    It is used for treatment and prevention of influenza A and B.

    X.J10-J18.J10   Influenza caused by an identified influenza virus

    Contraindications:

    Age up to 5 years, individual intolerance.

    Carefully:

    Pregnancy and lactation, hypersensitivity.

    Pregnancy and lactation:

    Recommendations for FDA - Category B. Applicable with caution, in cases where the expected effect exceeds the risk to the fetus and newborn.

    Dosing and Administration:

    Inhalation of 5 mg, the first day after 2 hours, then after 12 hours at the same time. The course of treatment is 5 days. Possible use with a preventive goal up to 1 month.

    The highest daily dose: 60 mg.

    The highest single dose: 5 mg.

    Side effects:

    Central and peripheral nervous system: headache, fatigue.

    Respiratory system: rhinitis, rarely - bronchospasm.

    Musculoskeletal system: myalgia, arthralgia.

    Dermatological reactions: hives.

    Allergic reactions.

    Overdose:

    Cases of overdose are not described.

    Treatment is symptomatic.

    Interaction:

    Inhalation bronchodilators are used before inhalation of zanamivir.

    Special instructions:

    It is recommended for use in the first two days of clinical manifestations of influenza.

    Instructions
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