Country: Bandaríkin
Tungumál: enska
Heimild: NLM (National Library of Medicine)
CLOBETASOL PROPIONATE (UNII: 779619577M) (CLOBETASOL - UNII:ADN79D536H)
Paddock Laboratories, LLC
CLOBETASOL PROPIONATE
CLOBETASOL PROPIONATE 0.5 mg in 1 mL
TOPICAL
PRESCRIPTION DRUG
Clobetasol Propionate Lotion, 0.05%, is a super-high potent topical corticosteroid formulation indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses only in patients 18 years of age or older. Treatment should be limited to 2 consecutive weeks. For moderate to severe plaque psoriasis, treatment may be extended for an additional 2 weeks for localized lesions (less than 10% body surface area) that have not sufficiently improved after the initial 2-week treatment. Any additional benefits of extending treatment should be weighed against the risk of hypothalamic-pituitary-adrenal (HPA) axis suppression before prescribing for more than 2 weeks. The total dosage should not exceed 50 g (50 mL or 1.75 fl. oz.) per week. Patients should be instructed to use Clobetasol Propionate Lotion, 0.05%, for the minimum amount of time necessary to achieve the desired results [see Dosage and Administration (2) ]. Use in patients under 18 years of age is not recommended due
Clobetasol Propionate Lotion, 0.05% is a white liquid, supplied in the following sizes: 2 fl oz/59 mL NDC 0574-2103-02 high density polyethylene bottles 4 fl oz/118 mL NDC 0574-2103-04 high density polyethylene bottles Store at USP controlled room temperature 68° to 77°F (20°-25°C), with excursions permitted between 59° and 86°F (15° - 30°C). Protect from freezing.
New Drug Application Authorized Generic
CLOBETASOL PROPIONATE- CLOBETASOL PROPIONATE LOTION PADDOCK LABORATORIES, LLC ---------- HIGHLIGHTS OF PRESCRIBING INFORMATION THESE HIGHLIGHTS DO NOT INCLUDE ALL THE INFORMATION NEEDED TO USE CLOBETASOL PROPIONATE LOTION, 0.05% SAFELY AND EFFECTIVELY. SEE FULL PRESCRIBING INFORMATION FOR CLOBETASOL PROPIONATE LOTION, 0.05%. CLOBETASOL PROPIONATE LOTION, 0.05%, FOR TOPICAL USE ONLY INITIAL U.S. APPROVAL: 1985 INDICATIONS AND USAGE Clobetasol Propionate Lotion, 0.05% is a corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses, in patients 18 years of age or older (1.1). (1) Limitations of Use: (1) • • • DOSAGE AND ADMINISTRATION • • • • DOSAGE FORMS AND STRENGTHS Lotion, 0.05%. (3) CONTRAINDICATIONS None (4) (4) WARNINGS AND PRECAUTIONS Clobetasol propionate is a highly potent topical corticosteroid that has been shown to suppress the hypothalamic-pituitary- adrenal (HPA) axis at the lowest doses tested (5.1) (5) Cushing’s syndrome, hyperglycemia and unmasking of latent diabetes mellitus can also result from systemic absorption of topical corticosteroids. (5.1) (5) Systemic absorption may require periodic evaluation for HPA axis suppression. Modify use if HPA axis suppression develops. (5.1) (5) Children may be more susceptible to systemic toxicity from use of topical corticosteroids (5.1, 8.4) (5) Local adverse reactions with topical corticosteroids may occur more frequently with the use of occlusive dressings and higher potency corticosteroids, including clobetasol propionate. These reactions include: folliculitis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, secondary infection, striae and miliaria. (5.2) (5) ADVERSE REACTIONS The most common adverse reactions (incidence > 1%) are skin atrophy, telangiectasia, discomfort skin and skin dry (6.1). TO REPORT SUSPECTED ADVERSE REACTIONS, CONTACT PERRIGO, MINNEAPOLIS, MN 55427 1-866-634-9120 OR FDA AT 1-800-FDA-1088 OR _WWW.FDA.GOV/MED Lestu allt skjalið