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A pharmacological and in vitro comparison of three oral cephalosporins.

作者信息

Wise R, Andrews J M, Dean S, Welling P G, Kendall M J

出版信息

J Antimicrob Chemother. 1979 Sep;5(5):601-7. doi: 10.1093/jac/5.5.601.

DOI:10.1093/jac/5.5.601
PMID:115833
Abstract

The pharmacology of cephradine, cephalexin and a new oral cephalosporin, cefaclor, has been compared in six volunteers. Cefaclor was absorbed rapidly and was cleared from the serum more rapidly than the other two agents. This was probably partially due to its instability in serum at body temperature, which was investigated. Against a wide range of common pathogens cefaclor was the more active oral cephalosporin. In particular the activity against Neisseria gonorrhoeae and Haemophilus influenzae was of interest.

摘要

相似文献

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A pharmacological and in vitro comparison of three oral cephalosporins.
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Br J Vener Dis. 1982 Jun;58(3):176-9. doi: 10.1136/sti.58.3.176.
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In vitro activity of Ro 15-8074 and Ro 19-5247, two orally administered cephalosporin metabolites.两种口服头孢菌素代谢产物Ro 15 - 8074和Ro 19 - 5247的体外活性
Antimicrob Agents Chemother. 1986 Jun;29(6):1067-72. doi: 10.1128/AAC.29.6.1067.