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Quadriderm RF Cream

US Brand Name Quadriderm RF
Generic Name Beclomethasone Dipropionate/ Clotrimazole/ Neomycin
Other Brand Name Quadriderm RF
Packing 5g, 10g
Manufacturer Fulford India
Form Cream
Strength Beclomethasone Dipropionate 0.025%/ Clotrimazole 1%/ Neomycin 0.5%
Country India

  • 10 gm $8.90
  • 5 gm 0.025% + 1% +0.5% Cream $3.35
Available online
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  • Quadriderm RF Cream box
  • Quadriderm Rf 10 Gm Cream (Fulford)
  • Quadriderm Rf Cream Manufacturer Information

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Introduction

Quadriderm RF Cream is an anti-fungal cream to treat itching and infections particularly for private areas. The skin near our thighs is likely to be infected by fungal problems that cause itching. It falls in the category of dermatological drugs. This medication is used for the treatment of the inflammatory signs of corticosteroid responsive dermatoses when complicated by secondary infection or when the possibility of such infection is suspected. Thus it treats balanoposthitis, chronic dermatitis of the extremities, contact dermatitis, photosensitivity dermatitis, eczematoid dermatitis, lichenified inquinal dermatophytosis, follicular dermatitis, paronychia, parakeratosis, anal pruritus, impetigo, intertrigo, neurodermatitis, angular stomatitis, and tinea infections such as tinea cruris, tinea pedis, and tinea corporis.

Drug Composition

Quadriderm Cream is composed of the active compound beclomethasone dipropionate, Clotrimazole and Neomycin for dermatologic use.

Dosage & Administration

Use a small quantity of Quadriderm RF Cream to cover completely the affected area two or three times daily, or as approved by the doctor. How often it will be used and for how long depend on the severity of the condition. In tinea pedis, you may need longer therapy (2 - 4 weeks). Children younger than 12 years of age should not use it. Stop using the drug when you see improvement. If you don't get better within 2 weeks, re-examine the diagnosis.

Drug Contraindications

Quadriderm RF Cream should not be applied in patients who have a history of sensitivity reactions to any of its components.

Side Effects

It has caused HPA axis suppression, linear growth retardation, Cushing's syndrome, intracranial hypertension and delayed weight gain in children using topical corticosteroids. The most common adverse effects are burning, itching irritation, and stinging sensation. Less common side effects are itching, cracking, skin atrophy, and fissuring of the skin, cracking, stinging, erythema, numbness of fingers, folliculitis, skin atrophy and telangiectasia.

The additional local side effects have been reported with topical corticosteroid, such as acneiform eruptions, dryness, hypopigmentation, allergic contact dermatitis, perioral dermatitis, secondary infection, striae, irritation, and miliaria.

Clotrimazole preparation causes erythema, burning, stinging, urticaria, pruritus, and edema and contact dermatitis. Neomycin rarely results in skin sensitization, ototoxicity and nephrotoxicity and most often allergic sensitization.

Necessary Safety Measures

Quadriderm RF Cream is not meant for ophthalmic use. Systemic absorption of topical corticosteroids can create reversible HPA axis suppression, glucocorticosteroid insufficiency, signs of cushing syndrome, glucosuria hyperglycemia by systemic absorption of topical corticosteroids while on therapy.

Patients who apply a topical steroid to a large surface area or to areas under occlusion should be assessed from time to time for checking of HPA axis suppression. Using it for loner period of time may rarely cause overgrowth of non-susceptible organisms. If you feel irritation or sensitization, discontinue treatment and institute appropriate therapy.

The safety of topical corticosteroid using in pregnant women is not confirmed. So drugs of this class should be used during pregnancy if it is quite essential. Don't use the drug in large amounts or for prolonged periods of time in pregnant patients. The mother should stop nursing or the drug using who breast feeds. Avoid this cream's contact with the eyes. Don't cover the treated skin area with bandage, or wrap so as to be occlusive unless directed by the doctor.