TY - JOUR
T1 - A double-blind evaluation of skin test suppression produced by two doses of terfenadine
AU - Bantz, Eric W.
AU - Dolen, William K.
AU - Nelson, Harold S.
N1 - Funding Information:
From Allergy-Immunology Service, Fitzsimons Army Medical Center, Aurora, Colo. Received for publication July 7, 1986. Accepted for publication Jan. 24, 1987. Reprint requests: William K. Dolen, M.D., MAJ, MC, USA, Allergy-Immunology Service, Fitzsimons Army Medical Center, Aurora, CO 80045-5001. The opinions or assertions contained herein are the private views of the authors and are not to be construed as official or as re-flecting the views of the Department of the Army or the De-partment of Defense. The protocol under which this study was conducted was approved by the Clinical Research and Human Use Committee of Fitzsimons Army Medical Center and the Office of the Surgeon General, United States Army.
PY - 1987/7
Y1 - 1987/7
N2 - For some patients, terfenadine, in the currently recommended dose of 60 mg twice daily (bid), may be only modestly effective in the treatment of allergic rhinitis. In a double-blind placebo-controlled crossover study of 12 patients, a larger dose (300 mg bid) was evaluated for its suppression of titrated skin tests to histamine and compound 48/80 to determine whether this regimen might result in greater suppression while it maintained the freedom from side effects of the presently recommended dose. In seven patients, skin test suppression by these two doses of terfenadine, each administered for 3 days, was compared to that produced in an earlier study by 3 days of treatment with chlorpheniramine (8 mg three times a day). The 300 mg bid terfenadine regimen produced significantly greater skin test suppression (p < 0.05) than the currently recommended 60 mg bid dose. There was no significant difference in side effects between the two doses, and neither active treatment regimen produced more side effects than placebo treatment. Both doses of terfenadine suppressed cutaneous reactivity significantly more than had chlorpheniramine. It is concluded that the presently recommended dose of terfenadine produces submaximal skin test suppression and that further studies are needed to investigate the clinical efficacy and safety of larger doses of terfenadine in the treatment of allergic rhinitis.
AB - For some patients, terfenadine, in the currently recommended dose of 60 mg twice daily (bid), may be only modestly effective in the treatment of allergic rhinitis. In a double-blind placebo-controlled crossover study of 12 patients, a larger dose (300 mg bid) was evaluated for its suppression of titrated skin tests to histamine and compound 48/80 to determine whether this regimen might result in greater suppression while it maintained the freedom from side effects of the presently recommended dose. In seven patients, skin test suppression by these two doses of terfenadine, each administered for 3 days, was compared to that produced in an earlier study by 3 days of treatment with chlorpheniramine (8 mg three times a day). The 300 mg bid terfenadine regimen produced significantly greater skin test suppression (p < 0.05) than the currently recommended 60 mg bid dose. There was no significant difference in side effects between the two doses, and neither active treatment regimen produced more side effects than placebo treatment. Both doses of terfenadine suppressed cutaneous reactivity significantly more than had chlorpheniramine. It is concluded that the presently recommended dose of terfenadine produces submaximal skin test suppression and that further studies are needed to investigate the clinical efficacy and safety of larger doses of terfenadine in the treatment of allergic rhinitis.
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U2 - 10.1016/S0091-6749(87)80198-7
DO - 10.1016/S0091-6749(87)80198-7
M3 - Article
C2 - 2885357
AN - SCOPUS:0023189616
SN - 0091-6749
VL - 80
SP - 99
EP - 103
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
IS - 1
ER -