Fluocinonide
(Redirected from Lidex)
Fluocinonide is a potent glucocorticoid used topically as an anti-inflammatory agent for the treatment of skin disorders such as eczema, psoriasis, rash, and dermatitis. It is a synthetic corticosteroid available in various forms, including creams, gels, ointments, and solutions. Fluocinonide works by reducing the actions of chemicals in the body that cause inflammation, redness, and swelling.
Pharmacology[edit | edit source]
Fluocinonide binds to the glucocorticoid receptor, leading to the activation of anti-inflammatory pathways and the suppression of pro-inflammatory cytokines. This action decreases the inflammatory response in the skin, providing relief from symptoms such as itching, redness, and swelling.
Indications[edit | edit source]
Fluocinonide is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses. It is one of the more potent corticosteroids available for topical use, making it a treatment option for more severe skin conditions that do not respond adequately to less potent corticosteroids.
Contraindications[edit | edit source]
The use of fluocinonide is contraindicated in patients with a history of hypersensitivity to any of the components of the formulation. It should not be used on facial skin, groin, or axillae unless directed by a physician, due to the increased risk of systemic absorption and side effects.
Side Effects[edit | edit source]
Common side effects of fluocinonide include burning, itching, irritation, dryness, folliculitis, hypertrichosis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, maceration of the skin, secondary infection, skin atrophy, striae, and miliaria. Long-term use or application to large surface areas can lead to systemic side effects due to absorption.
Administration and Dosage[edit | edit source]
Fluocinonide should be applied to the affected area as a thin film two to four times daily depending on the severity of the condition. The duration of treatment should be limited to two weeks for most conditions and should not exceed two consecutive weeks without the advice of a physician.
Precautions[edit | edit source]
Patients using fluocinonide should be advised not to use occlusive dressings unless directed by a physician, as this can increase systemic absorption. Caution should be exercised when used in children, as they are more susceptible to systemic toxicity. Pregnant or breastfeeding women should use fluocinonide only if the potential benefit justifies the potential risk to the fetus or nursing infant.
Interactions[edit | edit source]
There are no well-documented significant drug interactions with topical fluocinonide. However, concurrent use with other topical medications should be approached with caution to avoid potential additive effects or interference with the therapeutic effect of fluocinonide.
Pharmacokinetics[edit | edit source]
The extent of percutaneous absorption of topical corticosteroids, including fluocinonide, is determined by many factors including the vehicle, the integrity of the epidermal barrier, and the use of occlusive dressings. Systemic absorption of topical corticosteroids can produce reversible hypothalamic-pituitary-adrenal (HPA) axis suppression, manifestations of Cushing's syndrome, hyperglycemia, and glucosuria in some patients.
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Contributors: Prab R. Tumpati, MD