Active substanceAloe vera leavesAloe vera leaves
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  • Dosage form: & nbsphypodermic solution
    Composition:

    To obtain 1000 ml of the drug it is necessary:

    The active ingredient

    Aloe vera leaves - 360 g

    Auxiliary substances

    Sodium chloride 8.5 g

    Water of the day of injections - a sufficient number of obtaining 1000 ml of the preparation.

    Description:

    The liquid is from light yellow to brownish red with a characteristic odor. Opalescence or sediment is allowed, which forms an opalescence upon shaking.

    Pharmacotherapeutic group:Herbal origin means
    ATX: & nbsp

    S.01.B   Anti-inflammatory drugs

    Pharmacodynamics:

    Biogenic stimulant. Has adaptogenic, tonic, anti-inflammatory effect. Improves cellular metabolism, trophic and tissue regeneration, increases the overall nonspecific resistance of the body and the resistance of tissues, mucous membranes and skin to the action of damaging agents, accelerates the regeneration processes.It has a weak antimicrobial activity, immunostimulating properties.

    Indications:

    As a biogenic stimulant in the complex therapy of chronic diseases: in gastroenterology (peptic ulcer of the stomach and duodenum), respiratory tract (chronic bronchitis, pneumonia), in gynecology (adnexitis, endometritis), trophic ulcers.

    Contraindications:

    Hypersensitivity to the components of the drug, pregnancy, severe renal dysfunction, chronic heart failure, arterial hypertension, acute inflammatory diseases of the gastrointestinal tract, age to 18 years.

    Pregnancy and lactation:During the period of application of the drug, breastfeeding should be discontinued.
    Dosing and Administration:

    Subcutaneously.

    Daily 1 ml (the maximum daily dose of 3-4 ml). The course of treatment is 20-30 injections. On the recommendation of a doctor, it is possible to hold a second course in 2-3 months.

    Side effects:Allergic reactions, increased blood pressure, hyperthermia, diarrhea. If any of these side effects are aggravated, or if you notice any other side effects not listed in the instructions, tell your doctor.
    Overdose:In case of an overdose, dose-dependent side effects may be increased. Treatment: symptomatic.
    Interaction:

    Not described.

    Special instructions:When painful injections are administered previously 0.5 ml of 2% solution of novocaine.
    Effect on the ability to drive transp. cf. and fur:The use of the drug does not affect the ability to perform potentially dangerous activities requiring increased concentration and speed of psychomotor reactions (vehicle management, work with moving mechanisms, dispatcher and operator work).
    Form release / dosage:Solution for subcutaneous administration.
    Packaging:

    1 ml per ampoule of neutral glass or ampoules for ISO.

    5 ampoules per contour mesh package (with foil or paper, or without foil or paper).

    2 contour mesh packages are placed in a pack of cardboard.

    10 ampoules are placed in a pack of cardboard with a loose leaf of paper or with special pockets.

    In each pack you put the instruction on application and scarifier.

    When using ampoules with notches, rings and fracture points, the scarifiers do not insert into the pack.

    Storage conditions:

    In the dark place at a temperature of 12 to 25 ° C.

    Keep out of the reach of children.

    Shelf life:

    3 years.

    Do not use after the expiration date.

    Terms of leave from pharmacies:On prescription
    Registration number:LSR-007787/09
    Date of registration:05.10.2009 / 01.09.2016
    Expiration Date:Unlimited
    The owner of the registration certificate:VIFITEH, CJSC VIFITEH, CJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp12.07.2017
    Illustrated instructions
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