Severe Dermatologic Reactions Reported After Treatment with Tocainide

  1. JANET B. ARROWSMITH, M.D.;
  2. JOYCE I. CREAMER, B.S.N.; and
  3. LYNN BOSCO, M.D., M.P.H.
  1. U.S. Food and Drug Administration;
    Rockville, Maryland

    Excerpt

    Tocainide is a class I antiarrythmic drug with electrophysiologic characteristics similar to those of lidocaine. It is administered orally for suppression of symptomatic ventricular arrhythmias. Tocainide has been marketed in the United States since November 1984. (Tonocard; Merck Sharp & Dohme, West Point, Pennsylvania. The use of trade names is for purposes of product identification only and is not intended as product endorsement by the Food and Drug Administration [FDA] or the Department of Health and Human Services.) Among the well-recognized, serious adverse reactions reported after tocainide are blood dyscrasias and pulmonary fibrosis (1). We report a possible association between

    This 100-word excerpt has been provided in the absence of an abstract.

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