Diklogen® plus (Diclogen plus)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Dosage form: & nbspGel for external use
Composition:1 g of gel contains:
Active substances:
Diclofenac diethylamine - 11.6 mg is equivalent to the content of diclofenac sodium - 10 mg.
Methylsalicylate - 100 mg.
Racetenthol 50 mg.
Excipients: flax seed oil, carbomer 940, trolamine, propylene glycol, isopropanol, benzyl alcohol, butylhydroxyanisole, butylhydroxytoluene, polysorbate-60, hydrogenated castor oil, purified water.
Description:Semi-transparent gel from almost white to pale yellow with a characteristic odor.
Pharmacotherapeutic group:anti-inflammatory for topical use.
ATX: & nbsp
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    • Pharmacodynamics:Combined anti-inflammatory drug.
    Diclofenac and methyl salicylate are non-steroidal anti-inflammatory drugs (NSAIDs). They have a local analgesic, anti-inflammatory and anti-exsudative effect. The mechanism of action is due to the suppression of the synthesis of prostaglandins. With topical application reduce pain and inflammation in the joints, morning stiffness and swelling of the joints, contribute to an increase in the volume of movements. Menthol (rapecentol) causes irritation of nerve endings, has a local distracting and easy analgesic effect,causes a feeling of coolness in the place of application.
    Pharmacokinetics:With external application diclofenac and methyl salicylate are absorbed and penetrate into the subcutaneous tissue, muscle tissue and the joint capsule.
    Indications:For sympomatic therapy of diseases of the musculoskeletal system: rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, osteoarthritis of peripheral joints and spine, rheumatic soft tissue injuries, muscular pains of rheumatic and non-rheumatic origin, traumatic injuries of soft tissues.
    Contraindications:Hypersensitivity to diclofenac or other ingredients, to aspirin or other NSAIDs, anamnestic data fit bronchial, rhinitis, urticaria, after receiving aspirin or other NSAIDs, pregnancy (III trimester), lactation, infancy (up to 6 years) violation of the integrity of the skin at the site of the intended application.
    Carefully:Hepatic porphyria (exacerbation), erosive-ulcerative lesions of the gastrointestinal tract, severe violations of the liver and kidney function, chronic heart failure,old age, bronchial asthma, pregnancy (I and II trimester).
    Pregnancy and lactation:The drug is contraindicated in the III trimester of pregnancy. The question of the use of the drug in the first and second trimesters of pregnancy is decided individually. Due to the lack of experience in the use of Diclogen® Plus during lactation, the use of the drug in this period is not recommended.
    Dosing and Administration:Outwardly.
    For adults and children over 12 years old the drug is applied a thin layer over the inflammation focus 3-4 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 is 2-4 g (by volume comparable to the size of a large cherry).
    Children from 6 to 12 years of age should not be used more than 2 times a day, a single dose of the drug up to 2 g.
    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, hives, angioedema, bronchospastic reactions.
    Overdose:At external application in recommended doses extremely low systemic absorption of active components of a preparation does an overdose practically impossible.
    Interaction:Diclofenac can enhance the effect of drugs that cause photosensitivity.
    Clinically significant interaction with other drugs has not been described.
    Special instructions:The drug should be applied only to intact skin, avoiding getting on open wounds.
    After applying, do not apply an occlusive dressing.
    Do not allow the drug to enter the eyes and mucous membranes.
    Form release / dosage:Gel for external use.
    Packaging:30 g or 50 g of gel in an aluminum tube. 1 tube with instructions for use in a cardboard pack.
    Storage conditions:In dry, the dark place at a temperature of no higher than 30 ° C.
    Do not freeze.
    Keep out of the reach of children.
    Shelf life:3 years.
    Do not use the product after the date shown on the package.
    Terms of leave from pharmacies:On prescription
    Registration number:LSR-002602/10
    Date of registration:30.03.2010
    The owner of the registration certificate:Agio Pharmaceuticals Ltd.Agio Pharmaceuticals Ltd. India
    Manufacturer: & nbsp
    Representation: & nbspAgio Pharmaceuticals Ltd.Agio Pharmaceuticals Ltd.
    Information update date: & nbsp2016-02-06
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