Active substanceCromoglycic acidCromoglycic acid
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  • Dosage form: & nbspeye drops
    Composition:

    1 ml of the solution contains:

    Active component: sodium cromoglicate - 20, 00 mg;

    Auxiliary components: disodium edetate dihydrate 1.00 mg, sorbitol 40.00 mg, water for injection up to 1 ml.

    Description:

    Transparent, colorless or slightly yellowish solution.

    Pharmacotherapeutic group:Antiallergic agent - stabilizer of membranes of mast cells
    ATX: & nbsp

    S.01.G.X.01   Cromoglycic acid

    R.03.B.C.01   Cromoglycic acid

    Pharmacodynamics:

    Antiallergic, has a membrane-stabilizing effect, prevents the degranulation of mast cells and the release of histamine, bradykinin, leukotrienes and other biologically active substances. The drug is most effective for preventive use. A noticeable clinical effect in allergic eye diseases occurs in a few days or weeks.

    Pharmacokinetics:Absorption through the mucous membrane of the eye is negligible. Systemic bioavailability is less than 0.03%. Half-life T1/2 - 5-10 minutes.
    Indications:

    - Treatment (as part of complex therapy) and prevention allergic conjunctivitis (acute and chronic);

    - To alleviate and relieve irritation of the eye mucosa associated with allergic reactions:

    - on environmental factors and household chemicals;

    - on occupational hazards, including smoke, dust, fumes of solvents and other chemicals;

    - on the effect of cosmetics and medications;

    - on plants and pets.

    Contraindications:

    Hypersensitivity to the components of the drug, children's age (up to 4 years).

    Carefully:Not described.
    Pregnancy and lactation:

    Use during pregnancy is only possible if the intended benefit to the mother exceeds the potential risk to the fetus and the baby.

    The active substance of the drug can be excreted in breast milk. When used during lactation, breastfeeding should be discontinued for the period of treatment.

    In studies on animals with parenteral administration in high doses, a decrease in the weight of the fetus was observed.

    Dosing and Administration:

    Treatment

    Adults and children from the age of 4 Bury 1 drop in the conjunctival sac 4 times a day at intervals of 4-6 hours. If necessary, the dose can be increased to 6-8 instillations. Duration of application for allergic seasonal (acute) conjunctivitis - 7 days, with chronic allergic conjunctivitis - up to 4 weeks.

    Prevention

    Adults and children from the age of 4 Bury 1 drop of the drug 4 times a day in the conjunctival bag at regular intervals. The application begins 7-10 days before the possible development of seasonal allergic conjunctivitis and continues for another 7-10 days after the disappearance of the symptoms of the disease.

    Before each instillation it is necessary to remove the protective cap.

    Before the first use of the drug, flip the bottle vertically downwards, holding it with your thumb from below and press the middle and index fingers on the bottom (bottom) of the bottle several times until the first drop appears on the tip of the dropper. Thus, the dropper mechanism is activated and only one drop of the drug is withdrawn. After this, the vial is ready for further use. The special design of the dropper valve system ensures that the droplet is always the same size and the same speed of extraction even with very strong pressure on the base of the bottle.

    Tilt your head slightly back, slightly lift your lower eyelid and drip one drop into the conjunctival sac, as described above. Slowly close your eyes.

    After the procedure is finished, immediately seal the protective cap on the dropper.

    When instilling, avoid contact with the tip of the dropper with the surface of the eye and skin.

    Side effects:

    Temporary impairment of visual clarity, burning sensation, foreign body, dryness in the eye, swelling of the conjunctiva, lacrimation, meibomite.

    Allergic reactions: itching, mild tenderness and congestion hyperemia.

    Overdose:When topical application in the recommended dose of symptoms, there was no overdose.
    Interaction:

    Reduces the need for ophthalmic drugs containing glucocorticosteroids.

    Special instructions:

    Eye drops Allergo-KOMOD® do not contain a preservative, so it is possible to use in patients with intolerance to preservatives or wearing contact lenses. Contact lenses should be removed before instillation and wear not earlier than 15 minutes after instillation.

    After opening the vial and the first instillation, the drug can be used for 12 weeks. On the label of the vial and on the cardboard pack there is a special graph for filling: "Date of first use". It is recommended to record when you first dripped the drug.

    Effect on the ability to drive transp. cf. and fur:During the treatment period, care must be taken when driving vehicles and engaging in other potentially hazardous activities that require increased attention and speed of psychomotor reactions.
    Form release / dosage:

    Eye drops 2%.

    Packaging:For 10 ml in a plastic multi-dose vial with a protective cap. 1 bottle with instructions for use in a pack of cardboard
    Storage conditions:

    At a temperature of no higher than 25 ° C.

    Keep out of the reach of children!

    Shelf life:

    In the closed original packaging - 3 years.

    After opening the bottle, 12 weeks.

    Do not use after the expiry date printed on the package.

    Terms of leave from pharmacies:On prescription
    Registration number:LP-001158
    Date of registration:11.11.2011 / 10.01.2013
    Expiration Date:11.11.2016
    The owner of the registration certificate:Ursafarm Artsnaymittel GmbHUrsafarm Artsnaymittel GmbH Germany
    Manufacturer: & nbsp
    Representation: & nbspURSAFARM ARTSNAYMITTEL GmbH URSAFARM ARTSNAYMITTEL GmbH Germany
    Information update date: & nbsp08.07.2017
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