Febrofid gel 2.5% 50g

$10.56

Febrofid gel 2.5% 50g

Quantity:

Description

Composition
Active substance:
100 g of gel contains: ketoprofen lysine salt (in terms of ketoprofen) 2.50 g (1.60 g).
Excipients:
100 g of gel contains: macrogol-200 – 5.00 g methyl parahydroxybenzoate – 0,15 g propyl parahydroxybenzoate – 0.05 g Carbomer – 1.50 g, trolamine – 2.50 g Purified water up to 100 g
Description:
Clear or slightly opalescent colorless to light yellow gel.
Product form:
Gel for topical application of 2.5%.
30 g or 50 g aluminum tubes. 1 tube with instructions for use in a cardboard box.
Contraindications
• individual hypersensitivity to ketoprofen and / or other components of the drug, acetylsalicylic acid or other NSAIDs (indicating a history of bronchospasm, urticaria and rhinitis caused by the intake of acetylsalicylic acid); • moist dermatitis, eczema, infected abrasions, wounds, burns; • pregnancy (III trimester); • lactation; • children’s age (15 years).
Precautions: erosive and ulcerative lesions of the gastrointestinal tract; expressed human kidney and liver, chronic heart failure, bronchial asthma, pregnancy I-II trimester, hepatic porphyria.
Dosage
2.5%
Indications
• Acute and chronic inflammatory diseases of the musculoskeletal system: back pain, low back pain, sciatica, sciatica, lumbago, neuralgia, rheumatoid arthritis, joint syndrome in exacerbation of gout, spondylitis, osteoarthritis, bursitis, synovitis; • Muscle pain of rheumatic and rheumatic origin; • Injuries of the musculoskeletal system, including those associated with the athletic exercises: muscle pain, damage to ligaments and tendons, tendonitis, bruises and sprains, post-traumatic pain.
Interaction with other drugs
When applied topically as a gel ketoprofen dosage and other interactions are not set, however, it should consult a physician before using the gel if
You are taking other medicines.
Overdose
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).
Pharmacodynamics:
The mechanism of action of the drug associated with inhibition of prostaglandin synthesis.
Ketoprofen has anti-inflammatory, analgesic and antiexudative action.
In the form of gel provides a topical treatment of affected joints, tendons, ligaments, muscles. When the articular syndrome causes a weakening of joint pain at rest and during movement, reducing morning stiffness and swelling of joints.
Pharmacokinetics:
Ketoprofen lysine salt penetrates well through the skin and has a rapid local anti-inflammatory and analgesic effect. Bioavailability gel – approximately 5%. Not accumulates in the body.
Conditions of supply of pharmacies
Without recipe.
side effects
Local reactions: allergic dermatitis, eczema, skin redness, fotodermatit, bullous dermatitis, rash, purpura.
Systemic reactions: urticaria, generalized skin rash, swelling, photosensitivity, stomatitis.
At occurrence of any side effects you must stop using the product and seek medical advice.
special instructions
Avoid contact with the drug on the mucous membranes and eyes.
Do not use on damaged skin.
After drawing should not impose an occlusive bandage.
During prolonged use care must be taken in patients with severe liver failure and / or kidney.
If the rash appears necessary to stop treatment and spend the appropriate therapy.
Storage conditions
In the dark place at a temperature not higher than 25 ° C.
Keep out of the reach of children.
Dosing and Administration
Outwardly.
A small amount of gel (3-5 cm), 2-3 times per day applied to the skin in the inflamed or painful spot and easily rub.
No need to apply dry dressings, since the gel is well absorbed through the skin, does not contain coloring agents, leaves no oily stains, does not stain clothes.
It can be used in phonophoresis.
The duration of treatment should not exceed 14 days without consulting a doctor.
Information
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
Manufacturer

QUINACRINE

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