Nakashima M, Uematsu T, Takiguchi Y, Kanamaru M
Department of Pharmacology, Hamamatsu University School of Medicine, Japan.
J Clin Pharmacol. 1987 May-Jun;27(5):425-31. doi: 10.1002/j.1552-4604.1987.tb03043.x.
The tolerance to and pharmacokinetics of cefixime, a new oral cephalosporin, were evaluated in healthy volunteers given the drug in single doses of 50, 100 and 200 mg and repeated doses of 200 mg bid for 14 days. In the repeated-dose study, there were mild and transient subjective symptoms such as soft stools, diarrhea, and anorexia, which disappeared without additional treatment during the dosing period. Slight increases in eosinophil and serum amylase levels were also observed. The serum concentrations of cefixime peaked at 0.71, 1.17, and 2.08 micrograms/mL on average, four to five hours after dosing with 50, 100, and 200 mg, respectively, and the half-lives were 2.54, 2.38, and 2.29 hours. Serum concentrations and urinary recoveries after dosing with 100 mg were little affected by food ingestion. There was no evidence of cefixime accumulation in the body by repeated dosing since mean serum concentrations and urinary recoveries were almost the same on the first, third, seventh, and 14th days of dosing.
对一种新型口服头孢菌素头孢克肟,在健康志愿者中进行了单剂量50、100和200mg以及重复剂量200mg每日两次共14天给药后的耐受性和药代动力学评估。在重复给药研究中,出现了轻度短暂的主观症状,如软便、腹泻和厌食,在给药期间无需额外治疗即可消失。还观察到嗜酸性粒细胞和血清淀粉酶水平略有升高。头孢克肟的血清浓度在分别给予50、100和200mg剂量后4至5小时平均达到峰值,分别为0.71、1.17和2.08μg/mL,半衰期分别为2.54、2.38和2.29小时。进食对100mg给药后的血清浓度和尿回收率影响很小。重复给药后体内没有头孢克肟蓄积的证据,因为给药第1、3、7和14天的平均血清浓度和尿回收率几乎相同。