Artrozilen gel appearance. 5% 50g tuba


Artrozilen gel appearance. 5% 50g tuba



Active substance:
Ketoprofen lysine (ketoprofen lysine salt) 5.0 g (in terms of ketoprofen 3.125 g).
Carbomer 1.0 g, 1.9 g trolamine, polysorbate-80, 0.8 g, 95% ethanol 5.0 g Methyl parahydroxybenzoate 0.1 g, lavender and neroli flavor 0.2 g Purified water 86.0 ml.
Transparent gel of a light yellow color with a characteristic odor.
Product form:
Gel for topical application 5%.
50 g in an aluminum tube. The tube together with instructions for use in a stack of cardboard.
Hypersensitivity to ketoprofen and other ingredients, acetylsalicylic acid or other NSAIDs, fenofibrate, sunscreens (including history);
complete or partial combination of asthma, recurrent nasal polyposis or paranasal sinuses and intolerance to acetylsalicylic acid and other NSAIDs (including history); photosensitization reactions (history); violation of integrity of the skin (moist dermatitis, eczema, infected abrasions, wounds) at the site of the intended application; pregnancy (III trimester), breastfeeding, children’s age (up to 6 years).
Exposure to the sun’s rays, even on cloudy days, the solarium is contraindicated during treatment and for two weeks after the last treatment.
Hepatic porphyria (exacerbation), erosive and ulcerative lesions of the gastrointestinal tract,
heavy human liver and kidneys, chronic heart failure,
asthma, elderly, children (6 to 12 years), pregnancy (I and II
5 %
Diseases of the musculoskeletal system: rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, osteoarthritis of peripheral joints and spine, rheumatic soft tissue.
Muscular pain of rheumatic and rheumatic origin.
Traumatic (including sports), soft tissue damage.
The drug is intended for the symptomatic therapy reduce pain and inflammation at the time of use, does not affect the progression of the disease.
Interaction with other drugs
The drug can increase the effects of drugs that cause photosensitization.
Although the interaction with other drugs used topically or systemically,
it is unlikely in the case of prolonged treatment or treatment with high doses, it is necessary to take into account the possibility of competition between the absorbed ketoprofen and other drugs that are easily bound to plasma proteins.
Patients taking coumarin anticoagulants, it is advisable to carry out regular monitoring of the international normalized ratio (INR).
Very low systemic absorption of the active components of the preparation for external application makes it virtually impossible to overdose. Accidental ingestion of large amounts of gel (20 g) may cause systemic adverse reactions typical of NSAIDs. Necessary gastric lavage, administration of activated charcoal.
pharmachologic effect
Pharmacological group:
Nonsteroidal anti-inflammatory drug (NSAID).
It has a local anti-inflammatory, analgesic and antiekssudativnoe action. In the form of gel provides local therapeutic effect on affected joints, tendons,
ligaments, muscles. When the articular syndrome, reduces joint pain at rest and in motion,
morning stiffness and swelling of joints. Ketoprofen does not have a catabolic effect on articular cartilage.
When applied topically absorbed slowly. A dose of 50-150 mg every 5-8 h plasma levels creates 0.08-0.15 mcg / ml. Bioavailability gel – approximately 5%.
Pregnancy and breast-feeding
Use of the drug in the III trimester of pregnancy is contraindicated.
Use of the drug in the I and II trimesters of pregnancy only after consultation with your doctor if the intended benefits to the mother outweighs the potential risk to the fetus.
Use of the drug in the breastfeeding period is not recommended.
Conditions of supply of pharmacies
Without recipe.
side effects
Local skin reactions, such as erythema, rash, burning, itching. Sometimes these reactions can extend beyond the zone of application of the drug and very rarely can be severe and generalized.
Allergic reactions, dermatitis, contact eczema, urticaria, bullous dermatitis, photosensitivity reaction.
Very rarely occur systemic side reactions, such as impaired renal function.
In the case of any adverse event, should consult a doctor.
special instructions
The drug should only be applied to intact skin.
Avoid gel eyes and mucous membranes.
In order to avoid the manifestations of hypersensitivity and photosensitivity, it is recommended to avoid exposure of the skin to sunlight during the course of treatment and two weeks after its completion.
After the drug is necessary to wash your hands thoroughly.
Do not use occlusive dressing.
It should stop using the product in the event of any skin reaction while applying sunscreen or other cosmetics containing octocrylene.
Impact on the management of vehicles and mechanisms.
Information about the negative impact of the drug on the ability to drive and engage in other potentially hazardous activities that require concentration and speed of psychomotor reactions there.
Storage conditions
At temperatures above 25 ° C.
Keep out of the reach of children!
Dosing and Administration
Once using 1-1.5 g product (volume cherries). The drug is applied to the surface of the skin 2 times per day according to the size of the treated area and the prescribing physician gently massaging until complete absorption. In iontophoresis a drug is applied to the negative pole.
The dosage in children aged 6 to 12 years corresponds to that of adults, depending on the area of ​​application and the doctor’s recommendations.
The duration of the treatment – the drug is used both in acute and chronic diseases, for a period varying from a few days to 3-4 weeks.
Appearance may differ from that depicted in the picture. There are contraindications. You need to read the manual or consult with a specialist

Additional information

Weight0.100 kg


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