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匹氨西林的吸收与剂量的关系以及700毫克片剂的耐受性。

Absorption of pivampicillin as related to dose, and tolerability of a 700 mg tablet.

作者信息

Munkholm P, Olsen J, Hovgaard C, Hey H

机构信息

Dept. of Gastroenterology, University of Copenhagen, Denmark.

出版信息

Infection. 1993 Jan-Feb;21(1):30-3. doi: 10.1007/BF01739307.

Abstract

To evaluate the absorption and tolerability of a new formulation of pivampicillin administered as a 700 mg tablet, 14 healthy volunteers received single doses of 350, 500 and 700 mg p.o. Maximum serum concentrations (Cmax) of 5.73, 7.05 and 8.61 mg/l were obtained. The corresponding values for the area under the concentration/time curve (AUC) were 12.32, 18.99 and 25.30 mg/lxh. Concomitant intake of food increased the Cmax of the 700 mg tablet to 9.5 mg/l, while the AUC remained unchanged. Co-administration of the 700 mg pivampicillin dose with an antacid reduced the Cmax to 7.45 mg/l and the AUC to 17.92 mg/l x h. The tolerance of the 700 mg tablet was evaluated in a double-blind placebo-controlled study involving 57 patients. Six percent of the patients in each treatment group reported minor adverse reactions.

摘要

为评估以700毫克片剂形式给药的新制剂匹氨西林的吸收情况和耐受性,14名健康志愿者口服单剂量的350、500和700毫克匹氨西林。最大血清浓度(Cmax)分别为5.73、7.05和8.61毫克/升。浓度/时间曲线下面积(AUC)的相应值分别为12.32、18.99和25.30毫克/升·小时。同时进食使700毫克片剂的Cmax增加至9.5毫克/升,而AUC保持不变。700毫克匹氨西林剂量与抗酸剂共同给药使Cmax降至7.45毫克/升,AUC降至17.92毫克/升·小时。在一项涉及57名患者的双盲安慰剂对照研究中评估了700毫克片剂的耐受性。每个治疗组中有6%的患者报告有轻微不良反应。

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