Anti-Angin® Formula (Anti-Angin® Formula)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Active substanceTetracaine + Chlorhexidine + Ascorbic acidTetracaine + Chlorhexidine + Ascorbic acid
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  • Anti-Angin® Formula
    pills n / az. 
    VALEANT, LLC     Russia
  • Anti-Angin® Formula
    lozenges
    VALEANT, LLC     Russia
    • Dosage form: & nbsplozenges
    Composition:

    For one tablet:

    Active substances:

    Chlorhexidine diacetate 2.00 mg

    Tetracaine hydrochloride 0.20 mg

    Ascorbic acid - 50.00 mg

    Excipients: levomenthol, saccharin, sorbitol, silicon dioxide, magnesium stearate, flavoring "anise", flavor "mint", dye azorubin (H-122).

    Description:

    Tablets are flat, with a beveled edge, from pale pink to reddish pink with lighter and darker patches, with a specific odor. On both sides of the tablet are engraved "NP" against the background of a tree.

    Pharmacotherapeutic group:Antiseptic + local anesthetic
    ATX: & nbsp

    R.02.A.A.20   Other drugs

    R.02.A   Drugs for the treatment of throat diseases

    Pharmacodynamics:

    The antibacterial action of chlorhexidine is carried out due to non-specific binding to phospholipids of bacterial cell membranes.

    Chlorhexidine can have bactericidal and bacteriostatic effects, mainly against gram-positive bacteria and Candida albicans, and to a lesser extent, against gram-negative bacteria. Chlorhexidine particularly active in relation to Streptococcus mutans, Streptococcus salivarius, Escherichia coli, Selenomonas spp. and anaerobic bacteria. The drug is significantly less effective against such microorganisms as Streptococcus sanguis, Proteus, Pseudomonas, Klebsiella veillonella.

    Anesthetic tetracaine has a local anesthetic effect.

    Ascorbic acid is a cofactor in the process of collagen synthesis and tissue regeneration, strengthens immune responses and reduces the permeability of capillaries, thereby helping to reduce inflammation and edema of the mucous membranes of the oral cavity and pharynx.

    Indications:Prevention and treatment of infectious and inflammatory diseases of the oral cavity and pharynx (stomatitis, gingivitis, tonsillitis, pharyngitis, periodontitis, the initial stage of angina, a condition after tonsillectomy or tooth extraction, etc.).
    Contraindications:

    - Hypersensitivity to the components of the drug;

    - children under 5 years;

    - I trimester of pregnancy.

    Carefully:In II and III trimester of pregnancy according to the doctor's prescription, lactation period, diabetes mellitus, deficiency of glucose-6-phosphate dehydrogenase, hemochromatosis, sideroblastic anemia, thalassemia, hyperoxaluria, oxalosis and kidney stone disease.
    Dosing and Administration:

    Locally. Keep in mouth until complete resorption.

    Adults and children from 15 years of age: 6 tablets per day with an interval of 2 hours.

    Children from 5 to 10 years: 3 tablets a day with an interval of 4 hours.

    Children from 10 to 15 years: 4 tablets a day with an interval of 3 hours.

    Side effects:

    Allergic reactions.

    Intensive consumption can cause damage to the tooth enamel.

    Overdose:

    Symptoms of overdose: dizziness, general weakness, cyanosis, agitation, restlessness, muscle tremor, respiratory failure, nausea, vomiting.

    Treatment: gastric lavage, the appointment of salt laxatives; symptomatic therapy.

    Interaction:

    Tetracaine reduces the antibacterial activity of sulfanilamide preparations. Vasoconstrictors extend the effect and reduce the toxicity of tetracaine.

    Ascorbic acid increases the concentration of benzylpenicillin and tetracyclines in the blood, increases the risk of developing crystalluria in the treatment of short-acting salicylates and sulfonamides, and reduces the concentration of oral contraceptives in the blood.

    Special instructions:

    It is not recommended to apply simultaneously with oral and pharyngeal preparations containing iodine (Lugol's solution, povidone-iodine).

    Ascorbic acid, which is part of the drug, can change the results of some laboratory tests, which should be reported in the analysis.

    Effect on the ability to drive transp. cf. and fur:There is no information.
    Form release / dosage:

    Lozenges.

    Packaging:

    By 2, 4, 6, 8, 10, 12 tablets in a blister of PVC / Al.

    For 1, 2, 3, 4, 5, 10, 15 blisters in a cardboard box with instructions for use.
    Storage conditions:

    At a temperature of no higher than 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:Without recipe
    Registration number:P N 015460/01
    Date of registration:15.12.2008 / 01.06.2016
    Expiration Date:Unlimited
    The owner of the registration certificate:VALEANT, LLC VALEANT, LLC Russia
    Manufacturer: & nbsp
    Representation: & nbspVALEANT LLC VALEANT LLC Russia
    Information update date: & nbsp06.09.2017
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