首页> 外文期刊>The Journal of Clinical Pharmacology: Official Journal of the American College of Clinical Pharmacology >Effect of rofecoxib on prednisolone and prednisone pharmacokinetics in healthy subjects.
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Effect of rofecoxib on prednisolone and prednisone pharmacokinetics in healthy subjects.

机译:罗非昔布对健康受试者泼尼松龙和泼尼松药代动力学的影响。

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摘要

Patients receiving nonsteroidal anti-inflammatory drug therapy may also require administration of corticosteroids, particularly patients with rheumatoid arthritis. To investigate the effect of rofecoxib on the single-dose pharmacokinetics of oral prednisone and intravenous prednisolone, the authors conducted a randomized, double-blind, placebo-controlled crossover study in 12 healthy subjects. Oral rofecoxib (250.0 mg/day for 14 days) failed to influence prednisone or prednisolone pharmacokinetics after intravenous prednisolone or oral prednisone administration. The geometric mean ratio (GMR) (90% confidence interval) of prednisolone AUC infinity (rofecoxib/placebo) following intravenous and oral corticosteroid was 0.97 (0.94, 1.01) and 0.99 (0.91, 1.08), respectively. Similarly, the prednisone AUC infinity GMRs (rofecoxib/placebo) after intravenous and oral corticosteroid were 1.03 (0.95, 1.11) and 1.08 (0.92, 1.28), respectively. The absence of an effect of rofecoxib on the pharmacokinetics of oral prednisone or intravenous prednisolone indicates that no adjustment in dose of this corticosteroid is necessary when administered concurrently with rofecoxib.
机译:接受非甾体类抗炎药治疗的患者也可能需要服用皮质类固醇,尤其是类风湿关节炎患者。为了研究罗非昔布对口服泼尼松和静脉泼尼松龙的单剂量药代动力学的影响,作者对12名健康受试者进行了一项随机,双盲,安慰剂对照的交叉研究。口服泼尼松龙或口服泼尼松后,口服罗非昔布(250.0 mg /天,共14天)未能影响泼尼松或泼尼松龙的药代动力学。静脉和口服皮质类固醇激素后强的松龙AUC无限(罗非昔布/安慰剂)的几何平均比(GMR)(90%置信区间)分别为0.97(0.94,1.01)和0.99(0.91,1.08)。相似地,静脉和口服皮质类固醇治疗后,泼尼松AUC无穷大GMR(罗非考昔/安慰剂)分别为1.03(0.95,1.11)和1.08(0.92,1.28)。罗非考昔对口服泼尼松或静脉泼尼松龙的药代动力学没有影响,表明与罗非考昔同时给药时,无需调整这种皮质类固醇的剂量。

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