Effect of troglitazone on the pharmacokinetics of an oral contraceptive agent

被引:30
作者
Loi, CM
Stern, R
Koup, JR
Vassos, AB
Knowlton, P
Sedman, AJ
机构
[1] Warner Lambert Parke Davis, Pharmaceut Res Div, Dept Pharmacokinet Dynam & Metab, Ann Arbor, MI 48105 USA
[2] Warner Lambert Parke Davis, Pharmaceut Res Div, Dept Clin Pharmacol, Ann Arbor, MI 48105 USA
关键词
D O I
10.1177/00912709922007985
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Fifteen healthy women participated in a study to determine the effect of multiple doses of troglitazone on the pharmacokinetics of Ortho-Novum 1/35 (35 mu g ethinyl estradiol [EE] and 1 mg norethindrone [NE]). Participants received three cycles (21 days each of active drug followed by 7 days without medication) of Ortho-Novum. During the third cycle, participants also received troglitazone 600 mg qd for 22 days. Pharmacokinetic profiles of EE and NE were determined on day 21 of the second and third cycles. Progesterone and sex hormone binding globulin (SHBG) levels were also measured. Troglitazone decreased EE C-max and AUC((0-24)) by 32% and 29%, respectively. Likewise, troglitazone decreased NE C-max and AUC((0-24)) by 31% and 30%, respectively. Plasma SHBG concentrations increased from 113 nmol/L during cycle 2 to 220 nmol/L during cycle 3. Troglitazone reduced plasma unbound AUC for NE by 49%. Serum progesterone levels were lower than 1.5 ng/mL on all occasions. Thus, coadministration of troglitazone and Ortho-Novum decreases the systemic exposure to EE and NE. A higher dose of oral contraceptive or an alternate method of contraception should be considered for patients treated with troglitazone. (C) 1999 the American College of Clinical Pharmacology.
引用
收藏
页码:410 / 417
页数:8
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