Sodium bicarbonate (Sodium hydrocarbonate)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Active substanceSodium bicarbonateSodium bicarbonate
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    • Dosage form: & nbspPowder for solution for oral administration and topical application
    Composition:Sodium bicarbonate - 10 g.
    Description:

    White crystalline powder odorless, salty-alkaline taste. Aqueous solutions have an alkaline reaction.

    Pharmacotherapeutic group:Antacid agent
    ATX: & nbsp

    B.05.B.B   Solutions affecting the water-electrolyte balance

    Indications:

    Applied as a symptomatic antacid agent for heartburn, acidic eructation, feeling and severity in the epigastric region.

    Locally (in the form of rinses, rinses) are prescribed solutions of sodium bicarbonate in inflammatory diseases of the eyes, mucous membranes of the upper respiratory tract, etc., and also when acids get on the mucous membranes and skin.

    Contraindications:

    Individual intolerance, alkalosis, hypocalcemia, decreased acidity of gastric juice.

    Dosing and Administration:

    Inside, previously dissolved in water:

    adults of 0.5-1 g (about 1/3 of a teaspoonful) 4-6 times a day; children depending on the age of 0.1-0.75 g per reception. The drug is intended for short-term admission.

    For rinsings, washes, inhalations apply 0.5-2% solutions. To neutralize acids on the skin and mucous membranes, use a 2% solution.

    With prolonged use of the drug inside the development of alkalosis, accompanied by loss of appetite, nausea, vomiting, pain in the epigastric region, anxiety, headaches, and in some severe cases tetanic convulsions.
    Special instructions:

    The drug is not recommended for a long time to use inside. This is due to the fact that the neutralization of hydrochloric acid in the stomach with sodium hydrogen carbonate causes the release of carbon dioxide,which exerts an excitatory effect on the receptors of the gastric mucosa, increases the release of gastrin and may cause a secondary enhancement of the silver.

    Form release / dosage:

    Powder for solution for oral administration and topical application.

    Packaging:For 10 grams in heat-sealed bags.
    Storage conditions:

    In a dry place, at a temperature of no higher than 25 ° C.

    Shelf life:

    The drug should not be used after the expiry date indicated on the package.

    Terms of leave from pharmacies:Without recipe
    Registration number:P N000409 / 01-2001
    Date of registration:07.08.2008 / 17.11.2008
    Expiration Date:Unlimited
    The owner of the registration certificate:MOSCOW PHARMACEUTICAL FACTORY, CJSC MOSCOW PHARMACEUTICAL FACTORY, CJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp24.05.2018
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