|
|
|
EFLORNITHINE HYDROCHLORIDE (e-flor¢ni-theen) Vaniqa Classifications: SKIN AND MUCOUS MEMBRANE AGENT; DERMATOLOGICAL AGENT Prototype: Eflornithine Hydrochloride Pregnancy Category: C AVAILABILITY 13.9% cream ACTIONS/THERAPEUTIC EFFECTS Topical eflornithine inhibits enzyme activity in the skin that is required for hair growth. It results in retarding the rate of hair growth. PHARMACOKINETICS Absorption: <1% absorbed through intact skin. Metabolism: Not metabolized. Elimination: Excreted primarily in urine. Half-Life: 8 h. USES Reduction of unwanted facial hair in women. ROUTE & DOSAGE ADMINISTRATION
CONTRAINDICATIONS Hypersensitivity to eflornithine or its components; lactation, children <12y. PRECAUTIONS Pregnancy (category C). ADVERSE EFFECTS Body as Whole: Facial edema. CNS: Dizziness. GI: Dyspepsia, anorexia. Skin: Acne, pseudofolliculitis barbae, stinging, burning, pruritus, erythema, tingling, irritation, rash, alopecia, folliculitis, ingrown hair. NURSING IMPLICATIONS
Patient & Family Education
|