DIKLAK GEL

Active material: Diclofenac
When ATH: M02AA15
CCF: NSAIDs for outdoor use
ICD-10 codes (testimony): M05, M07, M15, M42, M45, M79, M79.1, T14.0, T14.3
When CSF: 05.01.02
Manufacturer: HEXAL AG (Germany)

Pharmaceutical form, composition and packaging

◊ Gel for external use 5% colorless or slightly yellow, clear, homogeneous and free of bubbles, with a characteristic odor of isopropyl alcohol.

Excipients: isopropyl alcohol, macrogol-7-glyceryl cocoate, gipromelloza, fragrant oil, Purified water.

50 g – aluminum tuba (1) – cardboard boxes.
100 g – aluminum tuba (1) – cardboard boxes.

Pharmacological action

NSAIDs for outdoor use. It has a pronounced analgesic and anti-inflammatory action. Nyeizbiratyelino glory glory ugnyetaya 1 e 2, It gives arachidonic acid metabolism and prostaglandin synthesis, It is the main link in the development of inflammation.

In the field of application Diklak^® It eliminates the pain and reduce swelling, associated with inflammation.

Pharmacokinetics

Data on the pharmacokinetics Diklak^® not provided.

Testimony

- Diseases of the musculoskeletal system: rheumatoid arthritis, psoriaticheskiy arthritis, ankylosing spondylitis, osteoarthritis of peripheral joints and spine;

- Soft tissue rheumatism;

- Muscle pain rheumatic and rheumatic origin;

- Traumatic soft tissue injuries.

Dosage regimen

The drug is used topically.

Adults and children over 6 years drug applied to the skin and lightly rubbed, multiplicity of application – 2-3 times / day. The required amount of the drug is dependent on the size of the affected area. A single dose of the drug – to 2 g (about 4 cm at wide-open mouth of the tube). After applying the medication should wash hands.

The duration of treatment depends on the indication and notes effect. After 2 weeks of treatment, patients should consult with your doctor.

Side effect

Local reactions: eczema, photosensitivity, contact dermatitis (itch, redness, swelling of the treated skin area, papules, vezikuly, peeling).

Systemic reactions: generalized skin rash, allergic reactions (hives, angioedema, bronhospasticskie reaction), photosensitivity.

Contraindications

- “Aspirin” asthma;

- Violation of the integrity of the skin;

- III trimester of pregnancy;

- Lactation (breast-feeding);

- Children up to age 6 years;

- Hypersensitivity to the drug;

- Hypersensitivity to aspirin or other NSAIDs.

FROM caution use in patients with hepatic porphyria (exacerbation), erosive and ulcerative lesions of the gastrointestinal tract, severe violations of liver and kidney function, in chronic heart failure, bronchial asthma, in elderly patients, I and II trimesters.

Pregnancy and lactation

The drug is contraindicated in the III trimester of pregnancy. The need for the appointment of the drug in I and II trimesters of pregnancy, the doctor will determine individually.

Experience with the drug Diklak^® lactation (breast-feeding) not available.

Cautions

Dyklak^® It should only be applied to intact skin, avoiding contact with open wounds. After application do not apply an occlusive dressing.

Do not allow the drug to the eyes and mucous membranes.

Overdose

The extremely low systemic absorption of the active ingredient of the drug when used externally makes it virtually impossible to overdose.

Drug Interactions

Dyklak^® may increase the effects of drugs, cause photosensitivity. No clinically significant interaction with other drugs has not been described.

Conditions of supply of pharmacies

The drug is resolved to application as an agent Valium holidays.

Conditions and terms

The drug should be stored at temperatures not exceeding 25 ° C. Shelf life – 3 year.