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S 6472颗粒制剂(缓释头孢克洛)用于慢性支气管炎的临床评价

[Clinical evaluation of S 6472 granule preparation (sustained-release cefaclor) in chronic bronchitis].

作者信息

Hiraga Y, Omichi M, Sasaoka S

机构信息

Department of Respiratory Diseases of Internal Medicine, Sapporo Railway Hospital.

出版信息

Jpn J Antibiot. 1988 Sep;41(9):1304-8.

PMID:3241328
Abstract

S 6472 granule preparation, a sustained-release cefaclor, was orally administered to 20 acutely exacerbated cases of chronic bronchitis at a daily dosage of 750 mg (titer) in 2 divided doses for a duration of 7-15 days and its clinical usefulness was evaluated. Clinical efficacies were good in 17 cases and fair in 3 cases, with a rate of efficacy of 85.0%. Organisms isolated from 13 patients were totalling 14 strains, i.e., 5 strains of Streptococcus pneumoniae, 3 strains of Branhamella catarrhalis, 2 strains of Streptococcus sp., 2 strains of Klebsiella oxytoca, 1 strain of Haemophilus influenzae and 1 strain of Staphylococcus aureus. All these strains, except the strains of Streptococcus sp., disappeared upon the administration of the drug. With regard to the safety, no side effects nor abnormal laboratory test values were encountered.

摘要

对20例慢性支气管炎急性加重期患者口服给予缓释头孢克洛制剂S 6472颗粒,每日剂量750mg(效价),分2次服用,疗程7 - 15天,并对其临床疗效进行评估。临床疗效为17例良好,3例尚可,有效率为85.0%。从13例患者中分离出的病原菌共14株,即肺炎链球菌5株、卡他布兰汉菌3株、链球菌属2株、产酸克雷伯菌2株、流感嗜血杆菌1株和金黄色葡萄球菌1株。除链球菌属菌株外,所有这些菌株在给药后均消失。关于安全性,未出现副作用,实验室检查值也未出现异常。

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