Efthymiopoulos C, Bramer S L, Maroli A, Blum B
Glaxo Wellcome R&D, Greenford, Middlesex, England.
Clin Pharmacokinet. 1997;33 Suppl 1:39-46. doi: 10.2165/00003088-199700331-00008.
Two phase I trials, each involving 16 healthy adult volunteers, were performed to investigate possible interactions between grepafloxacin and theophylline or warfarin. In the theophylline study, grepafloxacin 600 mg was administered once daily for 10 days to 12 volunteers who were receiving a maintenance dose of theophylline. This dose of theophylline was designed to produce mean serum theophylline concentrations of 7.5 mg/L; 4 volunteers received theophylline plus placebo. Pharmacokinetic parameters of theophylline were determined before grepafloxacin treatment and on day 10 of grepafloxacin or placebo administration. Peak theophylline concentrations and the area under the concentration-time curve increased significantly during grepafloxacin treatment, and apparent total clearance of theophylline was reduced by approximately 50%. No changes were observed in the placebo group and theophylline appeared to have no effect on the pharmacokinetics of grepafloxacin. In the warfarin study, grepafloxacin 600 mg was given once daily for 14 days to volunteers receiving a maintenance dose of warfarin. Warfarin was discontinued during the last 4 days of grepafloxacin administration. The pharmacodynamics of warfarin did not change after administration of grepafloxacin. Similarly, warfarin had no significant effect on the pharmacokinetics of grepafloxacin. We conclude that during treatment with grepafloxacin maintenance, doses of theophylline should be reduced by 50%, and we recommend that serum concentrations of theophylline be monitored during treatment with grepafloxacin. However, no dose adjustment is necessary for grepafloxacin when it is coadministered with theophylline, and dose adjustment does not seem to be required in concomitant treatment with grepafloxacin and warfarin.
进行了两项I期试验,每项试验涉及16名健康成年志愿者,以研究格帕沙星与茶碱或华法林之间可能的相互作用。在茶碱研究中,12名接受茶碱维持剂量的志愿者每天服用一次600毫克格帕沙星,持续10天。该剂量的茶碱旨在使血清茶碱平均浓度达到7.5毫克/升;4名志愿者接受茶碱加安慰剂。在格帕沙星治疗前以及格帕沙星或安慰剂给药第10天时测定茶碱的药代动力学参数。在格帕沙星治疗期间,茶碱的峰值浓度和浓度-时间曲线下面积显著增加,茶碱的表观总清除率降低了约50%。安慰剂组未观察到变化,茶碱似乎对格帕沙星的药代动力学没有影响。在华法林研究中,接受华法林维持剂量的志愿者每天服用一次600毫克格帕沙星,持续14天。在格帕沙星给药的最后4天停用华法林。服用格帕沙星后,华法林的药效学没有改变。同样,华法林对格帕沙星的药代动力学也没有显著影响。我们得出结论,在格帕沙星维持治疗期间,茶碱剂量应减少50%,我们建议在格帕沙星治疗期间监测茶碱的血清浓度。然而,格帕沙星与茶碱合用时无需调整剂量,格帕沙星与华法林联合治疗时似乎也无需调整剂量。