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

    Active substance:

    Aloe extract dry - 4 g

    (with the content of the sum of anthracene derivatives in terms of aloe-emodin not less than 0.5%)

    Excipients:

    Sodium chloride 8.5 g

    Water for injection - enough to obtain 1 liter of extract.

    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 some antimicrobial activity against streptococci, staphylococci, typhoid and dysentery rods, 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, pregnancy, severe renal dysfunction, chronic heart failure, arterial hypertension, acute inflammatory diseases of the gastrointestinal tract, children under 18 years.

    Pregnancy and lactation:

    It is recommended to stop breastfeeding during the period of application of the drug.

    Dosing and Administration:Subcutaneously. Daily 1 ml (the maximum daily dose - 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.
    Overdose:

    It is possible to increase dose-dependent side effects.

    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 performance of potentially hazardous activities requiring increased concentration of attention and speed of psychomotor reactions (vehicle management, work with moving mechanisms).

    Form release / dosage:

    Solution for subcutaneous administration.

    Packaging:

    1 ml per ampoule of neutral glass.

    For 10 ampoules together with instructions for use and a knife for opening ampoules or a scarifier ampoule in a box of cardboard.

    5 ampoules per contour cell packaging made of polyvinyl chloride film. 2 contoured cell packs together with instructions for use and a knife for opening ampoules or a scarifier ampullum in a pack of cardboard. When using ampoules with notches, rings and break points, the ampoule opener opener or ampoule scarifier is allowed not to be inserted.

    Storage conditions:

    In the dark place at a temperature of 15 to 25 ° C.

    Keep out of the reach of children.

    Shelf life:

    3 years.Do not use after the expiration date printed on the package.

    Terms of leave from pharmacies:On prescription
    Registration number:LP-001319
    Date of registration:02.12.2011 / 01.06.2015
    Expiration Date:Unlimited
    The owner of the registration certificate:DALHIMFARM, OJSC DALHIMFARM, OJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp12.07.2017
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