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Terbinafine

Terbinafine hydrochloride, sold as Lamisil tablets in the U.S., is often prescribed for the treatment of onychomycosis of the toenail or fingernail due to dermatophytes (Tinea unguium). more...

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It is also sold as a 1% cream or powder for use on suface infections such as jock itch (Tinea cruris) or athlete's foot (Tinea pedis).

Nail fungus infections live deep under the nail in the nail bed. Surface treatments may not be able to reach it in sufficient amounts, so terbinafine hydrochloride is given orally in tablet form, which is absorbed through the bloodstream to reach the infection; this method can cause hepatotoxicity, or liver damage, as well as other serious side effects, so those taking Lamisil tablets often have blood screenings every month. Many health insurance companies consider these infections to be a cosmetic problem, and either do not cover the cost of the months-long course of Lamisil, which can run into the thousands of dollars, or recommend use of less expensive alternatives like fluconazole.

The tablets contain the synthetic allylamine antifungal compound terbinafine hydrochloride, which is a white fine crystalline powder that is freely soluble in methanol and methylene chloride, soluble in ethanol, and slightly soluble in water. Chemically, it is (E)-N-(6,6-dimethyl-2-hepten-4-ynyl)-N-methyl-1- naphthalenemethanamine hydrochloride. The empirical formula C21H26CIN with a molecular weight of 327.90

  • Active Ingredients: Terbinafine hydrochloride (equivalent to 250 mg base)
  • Inactive Ingredients: Colloidal silicon dioxide, Hydroxypropyl methylcellulose USP, Sodium starch glycolate, Magnesium stearate, Microcrystalline cellulose.

Read more at Wikipedia.org


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Terbinafine Offers Advantages in Tinea Capitis - Brief Article
From Family Pratice News, 4/1/01 by Jennifer M. Wang

MIAMI BEACH -- Early experience suggests that terbinafine may eventually replace griseofulvin as the prescription of choice for the treatment of patients with tinea capitis, Dr. Ronald C. Hansen said at the annual Masters of Pediatrics conference sponsored by the University of Miami.

The current dosing guidelines for terbinafine therapy seem to be effective in spite of "wildly varying" allowances, said Dr. Hansen, who is a pediatric dermatologist at the University of Arizona in Tucson.

The rules of thumb for treating children specify the use of a quarter tablet per day for patients who weigh under 20 kg, half a tablet per day for those who weigh 20-40 kg, and one tablet per day for those who weigh more than 40 kg. There is no pediatric formulation for the drug, so the 250-mg tablets must be split by hand, he noted.

The 2- to 3-week time frame for terbinafine therapy translates into better patient compliance, compared with the 6 to 12-week regimen for griseofulvin. The new drug seems to be more effective than griseofulvin for Trichophyton tonsurans, which is the most common cause of tinea capitis in the United States, and terbinafine is free of griseofulvin's problem of resistance, Dr. Hansen said.

Terbinafine is poor therapy for fluorescent tinea stemming from M. canis, he added.

Other options for treating tinea capitis include itraconazole and fluconazole. However, they are not well studied for this indication and are not approved by the Food and Drug Administration. Further, itraconazole does not come in a pediatric dosage form.

Despite the efficacy of terbinafine, griseofulvin should-remain the first-line treatment for tinea capitis, because it is currently the only product that is FDA-approved for pediatric use, Dr. Hansen recommended.

COPYRIGHT 2001 International Medical News Group
COPYRIGHT 2001 Gale Group

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