Composition
- Active ingredient: Flugicasone propionate (micronized) – 0.50 mg;
- Auxiliary substances: Liquid paraffin-400.00 mg; Isopropyl myristate-50.00 mg; Cetostearyl alcohol-52.50 mg; Cetomacrogol 1000-7.50 mg; Propylene glycol-100.00 mg; Imidourea-2.00 mg; Sodium hydrophosphate dodecahydrate-1.50 mg; Citric acid monohydrate-0.50 mg; Purified water – up to 1.00 g.
Pharmacological action
Due to the limited absorption of fluticasone through the skin, the bioavailability of the drug with external use is very low. The oral bioavailability of fluticasone is close to zero due to the very low level of absorption in the gastrointestinal tract and extensive metabolism during the” first pass ” through the liver, which ensures a low level of systemic exposure in case of accidental ingestion of the drug.
Distribution
After entering the systemic circulation, fluticasone quickly enters the bile and is excreted through the intestines. The degree of binding to plasma proteins is quite high (91%). Fluticasone does not accumulate in the tissues and does not bind to melanin.
Metabolism
According to the results of preclinical and clinical studies, fluticasone has a high metabolic clearance followed by rapid elimination from the body. Thus, the drug that enters the systemic circulation through the skin is quickly inactivated. The main route of metabolism is hydrolysis to carboxylic acid; this metabolite has very weak glucocorticosteroid and anti-inflammatory activity.
Deduction
The rate of elimination of intravenously administered fluticasone propionate is linear in the dose range from 250 to 1000 micrograms and is characterized by high plasma clearance (CL=1.1 l / min).
The maximum plasma concentration decreases by approximately 98% over 3-4 hours, and only low plasma concentrations were associated with a final elimination half-life of 7.8 hours. Renal clearance of fluticasone propionate is insignificant (
Pharmacodynamics
Mechanism of action
Glucocorticosteroids for external use have anti-inflammatory properties. Anti-inflammatory properties are due to numerous mechanisms of inhibition of late-phase allergic reactions, including a decrease in the number of mast cells, a decrease in chemotaxis and activation of eosinophils, a decrease in cytokine production by lymphocytes, monocytes, mast cells and eosinophils, as well as inhibition of arachidonic acid metabolism.
Fluticasone belongs to glucocorticosteroids (corticosteroids) with a pronounced local anti-inflammatory effect. Fluticasone propionate is highly lipophilic, which allows it to penetrate the double lipid layer of the target cell and bind to glucocorticoid receptors in the cytoplasm.
In vitro studies have shown that fluticasone is characterized by high selectivity and affinity for glucocorticosteroid receptors.
The Fluticasone propionate-receptor complex stimulates or suppresses mRNA transcription and subsequent protein synthesis. The production of enzymes responsible for anti-inflammatory action increases, while the production of inflammatory mediators decreases.
The production of enzymes responsible for anti-inflammatory action increases, while the production of inflammatory mediators decreases. When applied to the skin, the probability of inhibition of the function of the hypothalamic-pituitary-adrenal system (HPA) is insignificant.
According to clinical studies, when fluticasone enters the systemic circulation, it is rapidly transformed in the liver to an inactive metabolite (17b-carboxylic acid), followed by rapid elimination from the body. Due to these properties, FeniVeyt has a high therapeutic index.
Pharmacodynamic effects
Fluticasone does not cause unexpected hormonal disorders, does not significantly affect the central and peripheral nervous systems, gastrointestinal tract, cardiovascular and respiratory systems.
Indications
FeniVate, which contains the effective glucocorticosteroid fluticasone, is used in adults and children aged 10 years and older to relieve symptoms associated with atopic dermatitis (eczema), seborrheic dermatitis, accompanied by irritation or allergic contact dermatitis.
Use during pregnancy and lactation
Fertility
There are no available data to assess the effect of corticosteroids for external use on human fertility. In animal studies, no effect of fluticasone propionate on fertility was found.
Pregnancy
There is limited data on the use of fluticasone during pregnancy. In studies of reproductive function in animals, undesirable effects characteristic of strong corticosteroids were observed only at a high level of systemic exposure.
As a result of preclinical studies, it was found that external use of corticosteroids in pregnant animals can cause fetal development abnormalities, however, the significance of this phenomenon for humans has not been established.
The use of the drug during pregnancy is not recommended, except in cases where the benefit to the mother exceeds the potential risk to the fetus and only under the supervision of a doctor. Before using during pregnancy, you should consult your doctor. In this case, the ointment should be applied in a minimum amount for the shortest possible period of time, sufficient for the manifestation of a clinical effect.
Breast-feeding period
The safety of corticosteroid therapy for external use during breastfeeding has not been established.
There are no available data to support the possibility of systemic absorption of corticosteroids for external use in a volume sufficient for their detection in breast milk.
As a result of preclinical studies, it was found that during breastfeeding, when administered subcutaneously in quantities sufficient for determination in plasma, fluticasone was detected in milk.
The use of the drug during breastfeeding is not recommended, except in cases where the intended benefit to the mother exceeds any possible risks to the child. Before using during breastfeeding, you should consult your doctor.
When using the drug during breastfeeding, the drug should not be applied to the area of the mammary glands to prevent its accidental ingestion by the child.
Contraindications
- Hypersensitivity to the Active ingredient or any other component that is part of the drug;
- Skin infections without prescribed therapy;
- Primary skin lesions of bacterial, viral and fungal etiology;
- Rosacea;
- Common acne;
- Perioral dermatitis;
- Perianal and genital pruritus;
- Pruritus without symptoms of inflammation;
- Children under 10 years of age.
Do not apply to closed areas of the skin (for example, on diaper rash or under occlusive dressings).
With caution:
Kidney failure, liver failure, elderly age, children’s age (from 10 to 12 years).
Side effects
The adverse reactions listed below are listed according to the lesion of organs and organ systems and frequency of occurrence. The frequency of occurrence is determined as follows: very common (≥ 1/10), common (≥ 1/100) and
the frequency of occurrence of adverse reactions
Infectious and parasitic diseases: Very rarely – Opportunistic infections.
Immune system disorders: Very rare-Hypersensitivity*: itching at the application site, rash, swelling.
Endocrine system disorders (HPA inhibition): Very rarely-Weight gain or obesity; Slow weight gain or stunted growth in children; Kushingoid features (for example, moon-shaped face, central obesity); Decreased endogenous cortisol concentration; Hyperglycemia or glucosuria; Arterial hypertension; Osteoporosis; Cataracts; Glaucoma.
Disorders of the skin and subcutaneous tissues
Often – Itching at the site of application of the ointment.
Infrequently-Burning sensation at the application site.
Very rarely – Thinning of the skin, atrophy, striae, telangiectasia, pigmentation changes, hypertrichosis, allergic contact dermatitis, exacerbation of symptoms of the underlying disease, pustular psoriasis, erythema, rash, urticaria.
* Local hypersensitivity reactions may resemble the symptoms of the disease for which this therapy is used.
You should inform your doctor if you experience any of the adverse reactions listed above. The decision on the future treatment strategy should be made by the doctor.
If any of the adverse reactions listed in the instructions get worse, or you notice any other adverse reactions not listed in the instructions, tell your doctor.
Interaction
Concomitant therapy with drugs that have an inhibitory effect on the CYP3A4 isoenzyme (for example, ritonavir, itraconazole) may lead to inhibition of corticosteroid metabolism, which is accompanied by increased systemic exposure. The degree of clinical significance of such interactions depends on the activity of the inhibitor of the CYP3A4 isoenzyme, the dose and method of administration of corticosteroids, but such an interaction is unlikely with the external method of application.
How to take it, course of administration and dosage
Externally. It is indicated for adults, the elderly, and children 10 years and older. The use of the cream is especially indicated for the treatment of wet or wet affected surfaces.Apply FeniVeyt cream in a thin layer in an amount not greater than necessary to cover the entire affected area, and gently rub 1 or 2 times a day until the effect is achieved, but not more than 4 weeks. It is necessary to allow sufficient time for FeniVeyt cream to be absorbed before applying the emollient. If the condition worsens or does not improve within 2 weeks, the treatment and diagnosis should be re-evaluated. When using the drug, care should be taken to ensure that the minimum amount of application that has a therapeutic effect is applied. Resumption of the initial symptoms of dermatosis may occur when corticosteroid therapy for external use is discontinued, especially in the case of highly active drugs.
Overdose
Symptoms
When applied externally, fluticasone can be absorbed in sufficient quantities to manifest a systemic effect. The probability of an acute overdose is extremely low, but with a chronic overdose or improper use of the drug FeniVeyt, signs of hypercorticism (Itsenko-Cushing syndrome) may develop.
Treatment
In case of fluticasone overdose, discontinuation of the drug is carried out gradually – by reducing the frequency of its application or switching to less active corticosteroids in order to avoid the risk of developing glucocorticoid insufficiency. If the clinical picture of drug overdose develops, symptomatic therapy is indicated.
Active ingredient
Fluticasone
Dosage form
cream
Best price for FeniVate cream for external use 0.05%, 15g in our online pharmacy!
Side effects of FeniVate cream for external use 0.05%, 15g.
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