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Antimicrobial Agents and Chemotherapy, March 1998, p. 695-697, Vol. 42, No. 3
Departments of Pharmacy
Services1 and
Medicine2 and
Clinical
Pharmacology Research Center,3 Bassett
Healthcare, Cooperstown, New York 13326-1394
Received 9 September 1997/Returned for modification 15 November
1997/Accepted 20 December 1997
Twelve healthy volunteers were enrolled in an open-label,
randomized, crossover study. Subjects received single doses of
theophylline (5 mg/kg) with and without multiple-dose terbinafine, and
11 blood samples were collected over 24 h. The study phases were
separated by a 4-week washout period. Theophylline serum data were
modeled via noncompartmental analysis. When the control phase (i.e., no terbinafine) was compared to the treatment phase (terbinafine), theophylline exposure (the area under the serum concentration-time curve from time zero to infinity) increased by 16% (P = 0.03), oral clearance decreased by 14% (P = 0.04),
and half-life increased by 24% (P = 0.002). No
significant changes in other theophylline pharmacokinetic parameters
were evident.
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Effect of Terbinafine on Theophylline
Pharmacokinetics in Healthy Volunteers
*
Corresponding author. Mailing address: Clinical
Pharmacology Research Center, Department of Pharmacy Services, Bassett
Healthcare, One Atwell Rd., Cooperstown, NY 13326-1394. Phone: (607)
547-3680. Fax: (607) 547-3629. E-mail: amsden{at}telenet.net.
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