If a favorable response does not occur promptly, use of Elocon Cream should be discontinued until the infection has been adequately controlled.Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice.In controlled clinical trials involving 319 subjects, the incidence of adverse reactions associated with the use of Elocon Cream was 1.6%. Apply a thin film of ELOCON Cream to the affected skin areas once daily. Select one or more newsletters to continue. ELOCON Cream may be used in pediatric patients 2 years of age or older. Long-term use of topical corticosteroids has not been studied in this population Because of a higher ratio of skin surface area to body mass, pediatric patients are at a greater risk than adults of HPA axis suppression and Cushing's syndrome when they are treated with topical corticosteroids. The following signs of skin atrophy were also observed among 97 subjects treated with Elocon Cream in a clinical trial: shininess, 4; telangiectasia, 1; loss of elasticity, 4; loss of normal skin markings, 4; thinness, 1; and bruising, 1.Because adverse reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.Postmarketing reports for local adverse reactions to topical corticosteroids include irritation, dryness, folliculitis, hypertrichosis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, secondary infection, striae, and miliaria. A focus group of optometrists who work with children came up with these guidelines to follow when prescribing for younger patients. It is not for oral, ophthalmic, or intravaginal use.Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.The easiest way to lookup drug information, identify pills, check interactions and set up your own personal medication records. It is not for oral, ophthalmic, or intravaginal use.Cream, 0.1%. The results show that the drug caused a slight lowering of adrenal corticosteroid secretion.If HPA axis suppression is noted, an attempt should be made to gradually withdraw the drug, to reduce the frequency of application, or to substitute a less potent corticosteroid. Pediatric patients may be more susceptible than adults to skin atrophy, including striae, when they are treated with topical corticosteroids. It is not known whether topical administration of corticosteroids could result in sufficient systemic absorption to produce detectable quantities in human milk. Similar effects were not observed at 7.5 mcg/kg. Such an observation should be corroborated with appropriate diagnostic patch testing.If concomitant skin infections are present or develop, an appropriate antifungal or antibacterial agent should be used. Fetal survival was reduced at 180 mcg/kg. Select one or more newsletters to continue. In a 2-year carcinogenicity study in Sprague Dawley rats, mometasone furoate demonstrated no statistically significant increase of tumors at inhalation doses up to 67 mcg/kg (approximately 0.04 times the estimated maximum clinical topical dose from Elocon Cream on a mcg/mMometasone furoate increased chromosomal aberrations in an In reproductive studies in rats, impairment of fertility was not produced in male or female rats by subcutaneous doses up to 15 mcg/kg (approximately 0.01 times the estimated maximum clinical topical dose from Elocon Cream on a mcg/mThe safety and efficacy of the Elocon Cream for the treatment of corticosteroid-responsive dermatoses were evaluated in two randomized, double-blind, vehicle-controlled clinical trials, one in psoriasis and one in atopic dermatitis. Guideline 3 ( Table 2 ) is based on the studies of Atkinson and colleagues, 20 , 46 which indicate functional improvements when children with hyperopia in the least hyperopic meridian of 3.50 D or more were given a partial prescription. Inflammation and/or other disease processes in the skin may increase percutaneous absorption.Long-term animal studies have not been performed to evaluate the carcinogenic potential of Elocon Cream. They are, therefore, also at greater risk of adrenal insufficiency during and/or after withdrawal of treatment. Not for oral, ophthalmic, or intravaginal use.Cream, 0.1 % Cream also... Application.Elocon Cream is for topical use only of 300 mcg/kg produced delays in,. Treated with topical corticosteroids human milk with children came up with these guidelines follow... Of age or older 300 mcg/kg produced delays in ossification, but no malformations treatment or after withdrawal of.... The Cream was applied without occlusion to at least 30 % of topical. 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