Clinical and pharmacological group: & nbsp

Glucocorticosteroids

Included in the formulation
АТХ:

H.02.A.B.03   Fluocortolone

Pharmacodynamics:

Glucocorticosteroid for external and topical application.Has anti-inflammatory, antiexudative, anti-allergic and antipruritic effect.

It binds to specific receptors located in the cytoplasm of cells of target organs and activates the synthesis of mRNA; induces the formation of lipocortin proteins, one of which is lipomodulin, inhibits the activity of phospholipase A2. The disruption of the formation of arachidonic acid actually means inhibition of the synthesis of prostaglandins, since arachidonic acid is a substrate for further metabolism along the cyclooxygenase pathway, and also along the lipoxygenase pathway, with appropriate inhibition of leukotriene synthesis.

The anti-inflammatory effect of fluocortolone is potentiated by its ability to inhibit the expression of COX-2 genes, which also leads to a decrease in the synthesis of prostaglandins in the inflammatory focus, including pro-inflammatory prostaglandins E2 and I2. Fluocortolone inhibits the expression of molecules of intercellular adhesion in the endothelium of blood vessels, violating the penetration of neutrophils and monocytes into the focus of inflammation.

With topical application fluocortolone prevents the accumulation of neutrophils,which leads to a decrease in the production of inflammatory exudates and lymphokines, inhibition of migration of macrophages, a reduction in inflammatory infiltration and granulation.

Pharmacokinetics:Absorption is 5% of the applied or administered amount of the drug. Fluorocortolone pivalate is hydrolyzed by esterases, enzymes of the inflammation focus, with the formation of fluocortolone, 11-ketofluocortolon and trimethylacetic acid. The half-lives from the plasma of fluocortolone and its metabolites after rectal administration were approximately 1.3 and 4 hours, respectively. Fluocortolone is excreted from the body in the form of metabolites mainly along with urine.
Indications:

For external use: various forms of eczema, contact dermatitis, neurodermatitis, seborrheic dermatitis, psoriasis, lichen planus, discoid lupus erythematosus, 1st degree burns, sunburn, insect bites.

For topical application (in combination with a local anesthetic): hemorrhoids, superficial anal fissures, proctitis.

IX.I80-I89.I83   Varicose veins

XII.L20-L30.L20   Atopic dermatitis

XII.L20-L30.L20.8   Other atopic dermatitis

XII.L20-L30.L21   Seborrheic dermatitis

XII.L20-L30.L23   Allergic contact dermatitis

XII.L20-L30.L24   Simple irritant contact dermatitis

XII.L20-L30.L28.0   Simple chronic lichen

XII.L40-L45.L40   Psoriasis

XII.L40-L45.L43   Lichen red flat

XII.L55-L59.L55   Sunburn

XII.L80-L99.L93.0   Discoid lupus erythematosus

XII.L20-L30.L29.3   Anogenital itching, unspecified

XII.L20-L30.L30.1   Dyshidrosis [pomfolix]

XII.L20-L30.L30.3   Infectious dermatitis

XII.L20-L30.L30.9   Dermatitis, unspecified

XII.L50-L54.L53   Other erythematous conditions

XII.L55-L59.L56.2   Photocontact dermatitis [berloque dermatitis]

XII.L80-L99.L87   Transepidermal perforated changes

XIII.M30-M36.M32   Systemic lupus erythematosus

XIX.T08-T14.T14.0   Superficial injury of unspecified area of ​​the body

XIX.T20-T32.T30   Thermal and chemical burns, unspecified

XIX.T66-T78.T78.4   Allergy, unspecified

Contraindications:Bacterial, viral, fungal skin diseases, skin tuberculosis, cutaneous manifestations of syphilis, skin tumors, pregnancy.
Carefully:Do not use for a long time, apply on large surfaces, directly on the calf sores with varicose veins.
Pregnancy and lactation:

Category of recommendations for FDA - S. Qualitative and well-controlled studies on humans and animals have not been conducted.

Contraindicated in pregnancy.

There is no information on the penetration into breast milk. Do not apply!

Dosing and Administration:Apply externally to affected areas 2-3 times a day. When the inflammation subsides, go for a single application. In children under the age of 4, the maximum duration of treatment is 3 weeks. In some cases, you can use an occlusive dressing.
Side effects:Steroid acne, purpura, skin atrophy, telangiectasia, burning, itching, irritation, dry skin, striae, perioral dermatitis, hypertrichosis. With long-term use (more than 4 weeks) and / or when applied to large surfaces, systemic side effects are possible.
Overdose:No data.
Interaction:In proctology, it is used in combination with a local anesthetic with cinchocaine.
Special instructions:

In children under the age of 4, the maximum duration of treatment is 3 weeks.

Avoid contact with ointment in the eyes.

Instructions
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