Chlorophyllipt® (Chlorophyllipt®)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Active substanceEucalyptus leaf extractEucalyptus leaf extract
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    • Dosage form: & nbspsolution for oral, local and external use of alcohol
    Composition:

    1 ml contains:

    active substance: chlorophyllipt, extract of thick (eucalyptus leaf extract), in terms of dry matter, with a content of a sum of chlorophylls of not less than 10% - 10 mg;

    Excipients: ethanol 96% - up to 1 ml.

    Description:

    The liquid is dark green in color. In the course of storage, precipitation may occur, forming a dense deposit on the walls and at the bottom of the vial or can.

    Pharmacotherapeutic group:antimicrobial agent of plant origin
    ATX: & nbsp

    D.06.B.X   Other antimicrobials

    Pharmacodynamics:Chlorophyllipt® is an extract from the leaves of eucalyptus, which has antibacterial activity against staphylococci, including antibiotic-resistant strains.
    Pharmacokinetics:

    Not studied.

    Indications:

    In the complex therapy of infection caused by staphylococci, in the treatment of burns, trophic ulcers, cervical erosions; intestinal carriage of staphylococci.

    Contraindications:

    Hypersensitivity to the components of the drug.

    When administered orally - the age of 18 years, pregnancy, the period of breastfeeding, liver disease, craniocerebral trauma, alcoholism, brain diseases.

    Pregnancy and lactation:

    During pregnancy and during breastfeeding, external and local use is possible if the expected benefit to the mother exceeds the potential risk to the fetus and the baby. It is necessary to consult a doctor.

    Dosing and Administration:

    Adults the drug is prescribed inside, topically, externally.

    Children under 18 years the drug is prescribed topically and externally.

    Inside. When used in adults with intestinal carriage of staphylococci, 5 ml of 1% alcohol solution diluted with 30 ml of water, 3 times a day for 40 minutes before meals every day.

    Outwardly (treatment of burns and trophic ulcers). 1% Alcohol solution is diluted 1: 5 with 0.2% solution of novocaine.

    Locally.

    With intestinal carriage of staphylococci Chlorophyllipt® is also prescribed rectally in enema (20 ml of 1% alcohol solution is diluted in 1 liter of water - this is a dose for one enema). The enema with the drug is put every two days. Children in volume (in ml), corresponding to age. The course of treatment consists of 10 procedures.

    In the treatment of cervical erosion pre-swab with all the folds of the vaginal mucosa and vaginal part of the cervix and lubricate 1% alcohol solution Chlorophyllipt® channel of the cervix and erosion. Use also syringing with a solution of the preparation (1 item spoon 1% alcohol solution per 1 liter of water). The course of treatment is 2 weeks.

    Side effects:Allergic reactions (swelling of the lips, mucous membranes, skin rashes).
    Overdose:To date, cases of overdose with proper application of the drug have not been recorded. It is possible to increase dose-dependent side effects.
    Interaction:

    Hydrogen peroxide. It should be borne in mind that when there are residues of hydrogen peroxide in the wound, Chlorophyllipt® precipitates, so after rinsing the wound with residual hydrogen peroxide, it should be removed with a sterile 0.9% solution of sodium chloride.

    Special instructions:

    When administered orally, a single dose of the drug contains 3.8 mg of ethanol, the daily dose of the drug contains 11.4 mg of ethanol (in terms of absolute alcohol).

    Effect on the ability to drive transp. cf. and fur:

    When using the drug inside it is necessary to refrain from driving motor vehicles and practicing potentially dangerous activities that require an increased concentration of attention and speed of psychomotor reactions (driving a car, etc.).

    Form release / dosage:

    Solution for oral administration, local and external use of alcohol, 1%.

    Packaging:

    To 100 ml in bottles or jars of dark glass ukuporennye with plastic stoppers and screwed caps or caps aluminum or in bottles of polymer with polymer caps.

    Vials are labeled with vials or cans.

    Each bottle or jar along with the instruction is put in a pack of cardboard.

    Storage conditions:

    Store in the original packaging at a temperature not exceeding 25 ° C.

    Keep out of the reach of children
    Shelf life:2 years.
    Do not use after the expiration date.
    Terms of leave from pharmacies:Without recipe
    Registration number:LS-001428
    Date of registration:12.05.2011 / 12.01.2016
    Manufacturer: & nbsp
    Representation: & nbspARTERIUM Corporation ARTERIUM Corporation Ukraine
    Information update date: & nbsp31.01.2016
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