Sulfoprocaine (Sulfoprokain)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Active substanceProcaine + Sulphocamphoric acidProcaine + Sulphocamphoric acid
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  • Sulfocamphocaine®
    solution for injections 
    PHARMSTANDART-UFIM VITAMIN FACTORY, OJSC     Russia
  • Sulfoprocaine
    solution for injections 
    BIOSINTEZ, PAO     Russia
    • Dosage form: & nbspinjection
    Composition:

    1 liter of solution contains:

    active substance: sulfo-camphoric acid (in terms of anhydrous) 49.6 g, procaine (novocaine base) 50.4 g;

    Excipients: water for injection up to 1 liter.

    Description:

    Transparent slightly yellowish liquid.

    Pharmacotherapeutic group:analeptic
    ATX: & nbsp

    R.07.A.B   Respiratory stimulants

    Pharmacodynamics:

    Combined drug. Stimulates the respiratory and vasomotor centers of the medulla oblongata. It has a direct effect on the myocardium, enhances the metabolic processes in it, improves its functions and raises its sensitivity to sympathetic impulses. Increases the tone of peripheral blood vessels. Improves pulmonary ventilation, pulmonary blood flow. Increases the secretion of bronchial glands.

    Due to its solubility in water, the drug is rapidly absorbed by subcutaneous and intramuscular injection. Does not cause the formation of infiltrates and complications (oleom).

    Indications:

    - Acute cardiac and respiratory failure;

    - cardiogenic and anaphylactic shock;

    - for stimulation of respiration in chronic respiratory and heart failure, pneumonia, infectious diseases.

    Contraindications:

    Hypersensitivity to the components of the drug (including procaine), pregnancy, lactation, age to 18 years (efficacy and safety not established).

    Carefully:

    Arterial hypotension.

    Dosing and Administration:

    Subcutaneously, intramuscularly 2 ml of 10% solution, if necessary, the frequency of administration is up to 2-3 times per day.

    In acute cases, the drug is administered intravenously (slowly struino or drip) in a single dose - 2.0 ml of a 10% solution.

    In chronic respiratory and heart failure, pneumonia, infectious diseases are administered subcutaneously or intramuscularly.

    The maximum daily dose of 12 ml of a 10% solution (1.2 g). If necessary, the course of treatment can be 20-30 days. Duration of application is set individually.

    Side effects:

    Reduction of blood pressure (especially in patients with initial arterial hypotension), dyspeptic disorders, allergic reactions.

    Interaction:

    Compatible with cardiac glycosides, steroid hormones, analgesics.

    Form release / dosage:

    Injection.

    Packaging:

    2 ml in ampoules.

    For 10 ampoules in a box of cardboard with corrugated septa of paper, paper or bag.

    By 5 ampoules in a contoured cell pack of a polyvinyl chloride film.

    2 contour squares in a pack of cardboard.

    Each instruction pack or box is supplied with instructions for use, an ampoule knife or a scarifier (when packing ampoules with a kink ring, notches and dots, the ampoule knife or scarifier does not insert).

    Storage conditions:

    In the dark place at a temperature of no higher than 25 ° C.

    Keep out of the reach of children.

    Shelf life:

    3 years.

    Do not use after the time specified on the package.

    Terms of leave from pharmacies:On prescription
    Registration number:LSR-001737/09
    Date of registration:10.03.2009
    The owner of the registration certificate:BIOSINTEZ, PAO BIOSINTEZ, PAO Russia
    Manufacturer: & nbsp
    Representation: & nbspBIOSINTEZ JSC BIOSINTEZ JSC Russia
    Information update date: & nbsp04.09.2015
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