Active substanceHuman albuminHuman albumin
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  • Dosage form: & nbspsolution for infusions
    Composition:

    100 ml of 10% solution contain:

    Albumin 10 g

    sodium caprylate 0.3 g

    sodium chloride 0.4 g

    water for injection up to 100 ml

    Description:Transparent liquid of light yellow color. A greenish shade is allowed.
    Pharmacotherapeutic group:Plasmasuberant
    ATX: & nbsp

    B.05.A.A.01   Albumen

    Pharmacodynamics:Plasma-replacing agent obtained by fractionating blood, plasma, placenta, serum from healthy donors. . Replenishes the deficiency of plasma albumin, supports the colloid-osmotic oncotic) blood pressure, rapidly increases blood pressure and bcc. Promotes the transition of fluid from tissues into the bloodstream, has detoxification properties.
    Indications:

    Shock (traumatic, operational, toxic), burns, accompanied by dehydration and "thickening" of blood; hypoproteinemia, hypoalbuminemia, developing with alimentary dystrophy, nephrotic syndrome, glomerulonephritis, liver cirrhosis, long-term ongoing purulent processes, gastrointestinal disease with impaired absorption or obstruction.

    Contraindications:Thrombosis, arterial hypertension, bleeding, heart failure II-III degree, severe anemia, increased individual sensitivity.
    Pregnancy and lactation:

    Albumin solution should be used during pregnancy and during breastfeeding only if the potential benefit to the mother exceeds the possible risk to the fetus or child.

    Dosing and Administration:

    Intravenously drip at a speed of 40-50 drops per minute, a single dose is determined individually, taking into account the age and severity of the patient's condition.

    In pediatric practice, albumin 10% is prescribed in a dose of not more than 3 ml / kg of body weight.

    Side effects:

    Allergic reactions (urticaria, anaphylactic shock), hyperthermia, pain in the lumbar region.

    Special instructions:

    Before use, it is necessary to make a visual inspection of the preparation and packaging: the solution must be transparent, not containing any inclusions, the glass packaging must be hermetic, without cracks. In the case history, it is necessary to register the label data (name of the preparation, manufacturer, serial number, production date).

    Administration of the drug during dehydration is possible only after preliminary ensuring sufficient intake of fluid (inside or parenterally).In the elderly, rapid administration of a 10% solution should be avoided, as this can lead to an overload of the cardiovascular system. Data on the use of albumin during lactation are absent.

    With the use of drugs made from human plasma, it is impossible to completely eliminate the risk of transmission of known and unknown yet viral infections.
    Form release / dosage:Solution for infusions 10%.
    Packaging:For 50, 100 and 200 ml in glass bottles for blood, transfusion and infusion preparations with a capacity of 50, 100 and 250 ml. Each bottle, along with instructions for use, is placed in a cardboard package.
    Storage conditions:At a temperature of +2 to +10 ° C.
    Shelf life:5 years.
    Terms of leave from pharmacies:On prescription
    Registration number:P N003840 / 01
    Date of registration:15.12.2009 / 09.01.2013
    Expiration Date:Unlimited
    The owner of the registration certificate:LIPETSK REGIONAL STATION OF BLOOD TRANSFUSION LIPETSK REGIONAL STATION OF BLOOD TRANSFUSION Russia
    Manufacturer: & nbsp
    Information update date: & nbsp15.07.2017
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