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The in vitro activity, human pharmacology, and clinical effectiveness of new beta-lactam antibiotics.

作者信息

Neu H C

出版信息

Annu Rev Pharmacol Toxicol. 1982;22:599-642. doi: 10.1146/annurev.pa.22.040182.003123.

DOI:10.1146/annurev.pa.22.040182.003123
PMID:6282190
Abstract
摘要

相似文献

1
The in vitro activity, human pharmacology, and clinical effectiveness of new beta-lactam antibiotics.新型β-内酰胺类抗生素的体外活性、人体药理学及临床疗效
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2
Antipseudomonal beta-lactams.抗假单胞菌β-内酰胺类抗生素
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[Susceptibility of recent clinical isolates of Pseudomonas aeruginosa and Serratia marcescens to cefotaxime, ceftizoxime, cefmenoxime, latamoxef and cefsulodin in comparison with other beta-lactam antibiotics and aminoglycosides].[铜绿假单胞菌和粘质沙雷氏菌近期临床分离株对头孢噻肟、头孢唑肟、头孢甲肟、拉氧头孢和头孢磺啶的敏感性与其他β-内酰胺类抗生素和氨基糖苷类抗生素的比较]
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4
Pharmacokinetics of the new cephalosporins.新型头孢菌素的药代动力学
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The in-vivo antibacterial activity of ceftazidime (Gr 20263)--a comparison with other new beta-lactam antibiotics and gentamicin.头孢他啶（Gr 20263）的体内抗菌活性——与其他新型β-内酰胺类抗生素及庆大霉素的比较
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[Antibacterial activities of new cephems against clinically isolated organisms (author's transl)].新型头孢菌素对临床分离菌的抗菌活性（作者译）
Jpn J Antibiot. 1982 Apr;35(4):1009-21.
8
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Comparison of the beta-lactamase stability and the in-vitro activity of cefoperazone, cefotaxime, cefsulodin, ceftazidime, moxalactam and ceftriaxone against Pseudomonas aeruginosa.头孢哌酮、头孢噻肟、头孢磺啶、头孢他啶、拉氧头孢和头孢曲松对铜绿假单胞菌的β-内酰胺酶稳定性及体外活性比较。
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Vet Res Commun. 1994;18(4):313-8. doi: 10.1007/BF01839199.
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In vitro antibacterial activity and beta-lactamase stability of E-0702, a new cephalosporin.新型头孢菌素E-0702的体外抗菌活性及β-内酰胺酶稳定性
Antimicrob Agents Chemother. 1983 Sep;24(3):313-20. doi: 10.1128/AAC.24.3.313.
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Antimicrob Agents Chemother. 1984 Jan;25(1):4-6. doi: 10.1128/AAC.25.1.4.
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Drugs. 1984 Jun;27(6):469-527. doi: 10.2165/00003495-198427060-00001.
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