Ibuprofen-Verte - instructions for use, dose, side effects, contraindications

Excipients: propylene glycol 10.0 g; ethanol 95% (ethyl alcohol 95%) - 15.0 g; carbomer - 1.25 g; dimethylsulfoxide - 2.5 g; trolamine (triethanolamine) - 5.5 g; methyl parahydroxybenzoate (methylparaben, nipagin) 0.15 g; orange flowers oil (neroli oil) - 0.05 g; lavender oil - 0.1 g; purified water - up to 100.0 g.

Description:Colorless or with a light yellow tinge transparent gel with a specific odor.

Opalescence and air bubbles are allowed.

Pharmacotherapeutic group:Non-steroidal anti-inflammatory drug (NSAID).

ATX: & nbsp

M.01.A.E.01 Ibuprofen

Indications:

Inflammatory and degenerative diseases of the musculoskeletal system; arthritis (rheumatoid, psoriatic); pain syndrome with rheumatism, with exacerbation of gout; humeroscapular periarthritis; Bechterew's disease (ankylosing spondylitis); deforming osteoarthritis; osteochondrosis with radicular syndrome; radiculitis; sciatica; Myalgia (rheumatic and non-rheumatic origin); lumbago; tendonitis, tendovaginitis, bursitis; traumas (sports, industrial, household) without disrupting the integrity of soft tissues (including bruises, posttraumatic swelling of soft tissues).

Contraindications:Increased individual sensitivity to ibuprofen or other components of the drug, including other NSAIDs; increased sensitivity to acetylsalicylic acid and other NSAIDs, manifested by an attack of bronchial asthma or other allergic reactions; wetting dermatoses,eczema; violation of the integrity of the skin (including infected wounds and abrasions); children's age (up to 6 years), pregnancy (III trimester).

Carefully:

Care should be taken when:

hepatic porphyria (exacerbation), erosive and ulcerative lesions of the gastrointestinal tract, severe violations of liver and kidney function, use in childhood (up to 12 years), pregnancy (I and II trimester), and lactation (breastfeeding).

The drug should not be applied to the open wound surface, damaged skin or mucous membranes (avoid contact with the eyes). After applying, do not apply an occlusive dressing.

After applying the drug, you should wash your hands thoroughly.

If the therapy is ineffective, you should consult your doctor.

In severe cases, it is recommended to combine local therapy with the intake of NSAIDs inside.

Pregnancy and lactation:The drug should not be used in the III trimester of pregnancy. Use in breastfeeding, in the I and II trimesters of pregnancy is possible after consultation with a doctor.

Dosing and Administration:

Outwardly. Adults and children from 12 years of a strip of gel length of 4 - 10 cm (corresponding to 50 - 125 mg ibuprofen) are applied to the affected area and carefully rubbed with light movements until completely absorbed.Repeated use of the drug is possible only after 4 hours and no more than 4 times a day. The required amount of the drug depends on the size of the painful area.

For children from 6 to 12 years, a strip of gel 2-4 cm long is applied to the lesion area no more than 3 times a day.

Duration of treatment - 2-3 weeks.

Side effects:Allergic reactions: possible - bronchospasm (with increased sensitivity to NSAIDs); rarely - skin hyperemia, rash, swelling, burning sensation, tingling or itching of the skin.

Overdose:

Symptoms: when using large amounts of gel on a large surface of the skin or entering the oral cavity, abdominal pain, nausea, vomiting, drowsiness, and headache may occur.

Treatment: remove gel residues from the skin surface or from the oral cavity. When large amounts of the drug enter the oral cavity, gastric lavage, the use of salt laxatives and symptomatic therapy are indicated.

Interaction:

Clinically significant interaction with other drugs has not been described.

Can enhance the systemic effect of other NSAIDs taken orally.

Effect on the ability to drive transp. cf. and fur:Application of gel Ibuprofen does not affect the activities requiring increased attention, coordination of movements, high speed of mental and physical reactions (including drivers of transport, persons servicing cars).

Form release / dosage:

Gel for external use 5%.

Packaging:By 20 g, 30 g, 50 g or 100 g in aluminum tubes. Each tube together with the instruction for use is placed in a pack of cardboard.

Storage conditions:Store at a temperature not exceeding 25 ° C. Keep out of the reach of children.

Shelf life:

2 years.

Do not use after expiry date.

Terms of leave from pharmacies:Without recipe

Registration number:LS-001967

Date of registration:20.09.2011

The owner of the registration certificate:VERTEKS, AO VERTEKS, AO Russia

Manufacturer: & nbsp

VERTEKS, AO Russia

Representation: & nbspVERTEKS CJSC VERTEKS CJSC Russia

Information update date: & nbsp20.09.2011

Illustrated instructions

Instructions

Ibuprofen-Verte (Ibuprofen-Verte)