Azulan (Azulan)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Active substanceChamomile flowersChamomile flowers
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  • Azulan
    solution locally inwards externally 
    VIFITEH, CJSC     Russia
  • Romazulan®
    solution locally inwards externally 
    K.O.Biopharm S.A.     Romania
    • Dosage form: & nbspsolution for oral, local and external use
    Composition:

    Composition per 100 g of the preparation

    Active components

    Chamomile extract liquid (44: 100) * - 95.881 g

    with the content of the sum of flavonoids in terms of routine 0.25%

    Gvayazulen

    in terms of 100% of the substance - 0.037 g

    Auxiliary component

    Tween 80 (polysorbate 80) - 4.082 g

    * Chamomile extract liquid (44: 100) was obtained from chamomile flowers (daisy peeled) - Chamomilla recutita (L.) Rausch. (Matricaria recutita L., M. chamomilla L.), the family of asters - Asteraceae; extractant - ethyl alcohol 50%, ammonia solution 10% to pH (8.0-8.5), ratio of raw materials: final extract - 44: 100.

    Description:

    The liquid is from brown with a greenish tint to a dark brown with a reddish tint of color with a characteristic odor. During storage, a deposit may occur.

    Pharmacotherapeutic group:Anti-inflammatory agent of plant origin
    ATX: & nbsp

    A.01.A.B   Antimicrobials for topical use in diseases of the oral cavity

    Pharmacodynamics:

    Combined drug. Has anti-inflammatory, antispasmodic and carminative action, has moderate antimicrobial properties.

    Pharmacokinetics:

    No data available.

    Indications:

    Inside: in complex therapy of gastritis, duodenitis, colitis, flatulence. Locally: with inflammatory diseases of the mucous membranes of the mouth (stomatitis, gingivitis, periodontitis), vaginitis.

    Outer: with inflammatory skin diseases (cracks, bites insects, etc.).

    Contraindications:

    Hypersensitivity to the components of the drug and plants of the family of astroids.

    Ingestion: pregnancy, the period of breastfeeding, children under 12 years.

    Carefully:

    Bronchial asthma, atopic dermatitis in history.

    When administered orally: liver disease, alcoholism, craniocerebral trauma, brain disease.

    If you have any of these diseases, consult a doctor before taking the drug.

    Dosing and Administration:

    Inside, adults and children from 12 years with gastrointestinal diseases: the drug is taken in a diluted form - 2.5 ml (1/2 a teaspoonful) on a glass (200 ml) of warm water 2-3 times a day. The course of treatment is 2-3 weeks. Conducting repeated courses of treatment is possible on the recommendation of a doctor. Outer in inflammatory skin diseases (bandages, lavage,compresses) and topically with inflammatory diseases of mucous membranes (in the form of microclysters of 50-100 ml, rinses, vaginal douches), the drug is used in diluted form - 7.5 ml (1/2 tablespoon) for 1 liter of water.

    Side effects:

    Allergic reactions are possible (contact dermatitis, allergic conjunctivitis, bronchospasm, Quincke's edema, anaphylactic shock).

    If any of the side effects listed in the manual are aggravated, or if you notice any other side effects not listed in the instructions, inform the doctor about it.

    Overdose:

    To date, cases of overdose have not been reported.

    Interaction:

    In connection with the inhibitory effect of the extract of chamomile on microsomal enzymes of the liver, simultaneous use of the drug with anticoagulants is not recommended (warfarin) due to an increased risk of bleeding.

    Special instructions:

    Before using the drug, you should consult your doctor. If the symptoms of the disease persist or worsen when the drug is used within 14 days, you should inform your doctor about it.

    The alcohol content in the preparation is not less than 32.0%.

    When administered inside the maximum single dose of the drug content of absolute ethyl alcohol (ethanol) is about 0.63 grams, in a maximum daily dose - about 1.89 g.

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

    During the period of treatment with taking the drug inside, care should be taken when carrying out potentially dangerous activities requiring increased concentration of attention and speed of psychomotor reactions (vehicle management, work with moving mechanisms, dispatcher and operator work).

    Form release / dosage:Solution for oral, local and external use.
    Packaging:

    To 50 or 100 ml in bottles of orange glass, sealed with stoppers and caps screwed on. To 100 ml in bottles of orange glass, ukuporennye caps aluminum with perforation with gaskets polymeric. 100 ml in bottles of polyethylene terephthalate brown with caps of the first opening control system. Each bottle, together with the instructions for use, is placed in a pack of cardboard.

    Storage conditions:

    In the dark place at a temperature of no higher than 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:LP-004311
    Date of registration:24.05.2017
    Expiration Date:24.05.2022
    The owner of the registration certificate:VIFITEH, CJSC VIFITEH, CJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp22.06.2017
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