Active substanceDiclofenacDiclofenac
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  • Dosage form: & nbspGel for external use.
    Composition:
    Active substance: diclofenac sodium - 5.0 g;

    Excipients: ethanol, propylene glycol, carbomer, methyl parahydroxybenzoate, trolamine, lavender oil, purified water.
    Description:Homogeneous, white or white with a yellowish or creamy shade gel with a specific odor.
    Pharmacotherapeutic group:Non-steroidal anti-inflammatory drug (NSAID).
    ATX: & nbsp

    S.01.B.C.03   Diclofenac

    M.01.A.B.05   Diclofenac

    Pharmacodynamics:
    The active component of the drug diclofenac - Non-steroidal anti-inflammatory drug (NSAID), which has pronounced analgesic (analgesic) and anti-inflammatory properties. Indiscriminately inhibiting cyclooxygenase type 1 and 2, disrupts the metabolism of arachidonic acid and the synthesis of prostaglandins, which are the main link in the development of inflammation.

    Gel Diclofenac 5% is used to eliminate the pain syndrome and reduce the swelling associated with the inflammatory process.When topical application causes weakening or disappearance of pain in joints at rest and during movement. Reduces the morning stiffness and swelling of the joints, contributes to an increase in the volume of movements.

    With the recommended method of applying the drug, no more than 6% of diclofenac is absorbed.
    Indications:
    - Post-traumatic inflammation of soft tissues and joints, for example due to stretching, overstrain and bruises.

    - Rheumatic diseases of soft tissues (tendovaginitis, bursitis, lesion of periarticular tissues);

    - Pain syndrome and swelling associated with diseases of the muscles and joints (rheumatoid arthritis, osteoarthritis, radiculitis, lumbago, sciatica, muscular pain of rheumatic and non-rheumatic origin).
    Contraindications:
    Hypersensitivity to diclofenac or other components of the drug, acetylsalicylic acid or other NSAIDs, anamnestic data on a bronchial asthma attack, rhinitis, urticaria after taking acetylsalicylic acid or other NSAIDs, pregnancy (III trimester), lactation period, children's age (up to 6 years), violation the integrity of the skin.


    Carefully:
    hepatic porphyria (exacerbation), erosive and ulcerative lesions of the gastrointestinal tract, severe violations of the liver and kidney function, chronic heart failure, bronchial asthma, blood clotting disorders (including hemophilia, lengthening bleeding time, tendency to bleeding), elderly age, pregnancy I and II trimester.

    Pregnancy and lactation:The drug should not be used in the III trimester of pregnancy. Experience in using the drug during lactation is not available. Use in I and II trimesters is possible only after consultation with a doctor.
    Dosing and Administration:
    Outwardly. Adults and children over 12 years of age, the drug is applied to the skin 2-3 times a day and lightly rubbed. The required amount of the drug depends on the size of the painful area. A single dose of the drug - up to 2 g (about 4 cm with a fully open neck of the tube). Children from 6 to 12 years of age should not be used more than 2 times a day, a single dose of the drug to 1 g (about 2 cm with a fully open neck of the tube). After applying the product, the hands should be washed.

    The duration of treatment depends on the indications and the effect observed. After 2 weeks of use, consult a physician.
    Side effects:
    Local reactions: eczema, photosensitivity, contact dermatitis (itching, redness, swelling of the treated area of ​​the skin, papules, vesicles, peeling).

    Systemic reactions: generalized skin rash, allergic reactions (hives, angioedema, bronchospastic reactions), photosensitization.
    Overdose:Extremely low systemic absorption of active components of the drug with external application makes an overdose almost impossible. In case of accidental ingestion of large amounts of gel (more than 20 g), systemic undesirable reactions characteristic of NSAIDs are possible. It is necessary to wash the stomach, taking activated charcoal.
    Interaction:The drug may enhance the effect of drugs that cause photosensitivity. Clinically significant interaction with other drugs has not been described.
    Special instructions:
    The gel should only be applied to intact skin, avoiding contact with open wounds. After applying, do not apply an occlusive dressing. Do not allow the product to get into the eyes and mucous membranes.

    With prolonged use of large amounts of the drug, it is impossible to exclude the occurrence of systemic side effects, characteristic for NSAIDs.
    Form release / dosage:
    Gel for external use 5%.
    Packaging:
    For 30 g, 50 g, 100 g in aluminum tubes with screwed polymeric buds or laminated tubing with screwed polymer bush.

    Each tube with instructions for use in a pack of cardboard.

    Storage conditions:
    At a temperature of 15 to 25 ° C. Freezing is not allowed.

    Keep out of the reach of children.
    Shelf life:3 years. Do not use the product after the expiry date printed on the package.
    Terms of leave from pharmacies:Without recipe
    Registration number:LSR-000077
    Date of registration:28.05.2007
    The owner of the registration certificate:SYNTHESIS, OJSC SYNTHESIS, OJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp10.03.2016
    Illustrated instructions
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