Powercort (Cream) Instructions for Use
Marketing Authorization Holder
Glenmark Pharmaceuticals, Ltd. (India)
ATC Code
D07AD01 (Clobetasol)
Active Substance
Clobetasol (Rec.INN registered by WHO)
Dosage Form
| Powercort | Cream for external use 0.05%: tube 15 g |
Dosage Form, Packaging, and Composition
Cream for external use homogeneous, white in color.
| 100 g | |
| Clobetasol propionate | 0.05 g |
Excipients: white soft paraffin, liquid paraffin, cetomacrogol, anhydrous disodium phosphate, sodium dihydrogen phosphate dihydrate, butylated hydroxytoluene, methylparaben, propylparaben, propylene glycol, purified water.
15 g – aluminum tubes (1) – cardboard packs.
Clinical-Pharmacological Group
Topical corticosteroids for external use
Pharmacotherapeutic Group
Corticosteroids used in dermatology; corticosteroids; corticosteroids with very high activity (group IV)
Pharmacological Action
Topical glucocorticosteroid.
It prevents the marginal accumulation of neutrophils, reduces inflammatory exudation and the production of lymphokines, inhibits macrophage migration, reduces the intensity of infiltration and granulation processes, and exerts local anti-inflammatory, antipruritic, antiallergic, and anti-exudative effects.
Pharmacokinetics
After application of clobetasol in topical dosage forms to healthy skin, the mean Cmax of the active substance is about 0.63 ng/mL and is reached in plasma approximately 8-13 hours later.
In patients with psoriasis and eczema, the mean Cmax is reached approximately 3 hours after application and is 2.3-4.6 ng/mL.
When applied to large areas of the skin, absorption is possible (damage to the integrity or inflammation of the skin enhances absorption) and systemic effects may occur.
It is metabolized mainly in the liver, a small part – in the kidneys. It is excreted in the urine.
Indications
Psoriasis (except for extensive plaque psoriasis), prevention and treatment of relapses of scalp psoriasis (except for extensive plaque psoriasis); eczema, lichen planus, discoid lupus erythematosus; skin diseases resistant to therapy with less potent topical glucocorticosteroids.
ICD codes
| ICD-10 code | Indication |
| L20.8 | Other atopic dermatitis (neurodermatitis, eczema) |
| L30.0 | Nummular eczema |
| L40 | Psoriasis |
| L43 | Lichen planus |
| L93.0 | Discoid lupus erythematosus |
| ICD-11 code | Indication |
| 9A06.70 | Atopic eczema of the eyelids |
| EA80.0 | Infantile atopic eczema |
| EA80.1 | Childhood atopic eczema |
| EA80.2 | Adult atopic eczema |
| EA80.Z | Atopic eczema, unspecified |
| EA82 | Nummular dermatitis |
| EA85.20 | Atopic hand eczema |
| EA90.Z | Psoriasis, unspecified |
| EA91.Z | Lichen planus, unspecified type |
Dosage Regimen
| The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen. |
Apply a thin layer of cream to the affected skin areas once or twice daily.
Gently rub in until fully absorbed. Limit application to the smallest area necessary.
The total treatment duration should not exceed four weeks. Use the shortest duration sufficient to control symptoms.
For scalp psoriasis, apply a thin layer to the affected areas of the scalp once daily.
Do not use more than 50 grams per week in adults. Avoid occlusive dressings unless specifically directed by a physician.
In pediatric patients, use the minimal effective amount and duration. Medical supervision is required at least weekly.
Discontinue use once control is achieved. If no improvement is seen within two weeks, re-evaluate the diagnosis.
Do not apply to the face, groin, or axillae unless prescribed for those specific areas.
Avoid contact with eyes and eyelids. If contact occurs, rinse immediately with copious water.
Wash hands thoroughly after application, unless the hands are the treated area.
Adverse Reactions
Dermatological reactions burning, skin itching, steroid acne, dry skin, folliculitis, skin soreness, psoriasis (exacerbation), alopecia, allergic contact dermatitis, erythema; with long-term use – weakening of the skin barrier function; with long-term use in high doses – atrophic changes in the skin, in particular, its thinning, appearance of atrophic striae, dilation of superficial blood vessels, especially when applying occlusive dressings and when applying the product to skinfold areas (the risk of this complication is increased in young children, in which case a diaper can act as an occlusive dressing); skin pigmentation and hypertrichosis may develop.
Gastrointestinal system when applied to large surfaces, gastritis, ulceration of the gastrointestinal mucosa are possible.
Endocrine system when applied to large surfaces, symptoms of hypercorticism, suppression of adrenal function, Cushing’s syndrome are possible.
Organ of vision eye pain/burning, eye irritation, eye strain, glaucoma are possible.
Nervous system: headache.
Other in rare cases – exacerbation of disease symptoms.
Contraindications
Hypersensitivity to clobetasol; rosacea, acne vulgaris, skin cancer, nodular prurigo of Hyde, perioral dermatitis, perianal and genital pruritus, skin manifestations of syphilis, diaper rash, bacterial, viral, and fungal skin diseases (including herpes simplex, chickenpox, skin tuberculosis, actinomycosis), extensive plaque and pustular psoriasis; application of the product to the eyes and eyelids (risk of glaucoma, cataract); pregnancy, lactation (breastfeeding); children’s age – depending on the dosage form.
Use in Pregnancy and Lactation
Contraindicated for use during pregnancy and lactation (breastfeeding).
Pediatric Use
Use in children is possible according to indications, in age-appropriate recommended doses and dosage forms.
It is necessary to strictly follow the instructions in the clobetasol drug leaflets regarding contraindications for use in children of different ages for specific clobetasol dosage forms.
Special Precautions
In rare cases, treatment of psoriasis with topical glucocorticosteroids (or their withdrawal) provokes the development of pustular psoriasis.
Long-term prescription of topical glucocorticosteroids in large doses or their application to extensive areas of the skin may be accompanied by systemic absorption with subsequent development of hypercorticism symptoms.
The risk of this complication is increased in children, especially when using an occlusive dressing, in which case a diaper can act as such a dressing.
In such cases, it is necessary to enhance medical supervision and regularly examine the patient for suppression of the hypothalamic-pituitary-adrenal system.
Provided that clobetasol is used in adults at a dose not exceeding 50 g per week, suppression of pituitary and adrenal function is transient with rapid recovery immediately after the end of the treatment course.
Clobetasol is preferably used short-term.
The use of topical glucocorticosteroids for a prolonged period should be avoided, as this may lead to suppression of adrenal function.
Atrophic skin changes may appear on the face more often than on other parts of the body as a result of long-term use of topical glucocorticosteroids.
Clobetasol should not be applied to the periorbital area, as this may cause the development of glaucoma.
Treatment of psoriasis with topical glucocorticosteroids may be accompanied by the development of disease relapse, tolerance, generalized pustular form of the disease, local or systemic toxic reactions due to impaired skin barrier function, therefore patient monitoring is especially important.
In case of secondary infection, appropriate antibacterial therapy should be administered.
If any signs of infection generalization appear, topical use of glucocorticosteroids should be discontinued and appropriate treatment with antibacterial drugs should be carried out.
The warm, moist conditions created by applying an occlusive dressing promote the occurrence of bacterial infection, so the skin must be cleaned before applying a new dressing.
Clobetasol in the form of a shampoo is indicated only for the treatment of scalp psoriasis; it should not be applied to other parts of the body and skin areas prone to chafing (armpits, genital and anal areas) and to erosive skin areas, as this increases the risk of local adverse reactions such as atrophic skin changes, telangiectasias, or steroid-induced dermatitis.
If shampoo gets into the eyes, they should be rinsed immediately with plenty of water.
Use in pediatrics
The use of clobetasol in children requires medical supervision at least once a week.
The use of topical glucocorticosteroids for a prolonged period in young children should be avoided, as this may lead to suppression of adrenal function.
Storage Conditions
Store at 2°C (36°F) to 25°C (77°F). Keep in original packaging, protected from light. Keep out of reach of children.
Dispensing Status
Rx Only
Important Safety Information
This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.
Medical Disclaimer