Axile头孢呋辛。

M A Marx, W K Fant
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引用次数: 0

摘要

头孢呋辛酯是头孢呋辛的口服活性前药制剂,吸收后立即脱酯化释放头孢呋辛。头孢呋辛酯对许多革兰氏阳性和一些革兰氏阴性微生物具有体外抗菌谱。其β -内酰胺酶的稳定性使其可用于治疗由产生β -内酰胺酶的流感嗜血杆菌、卡他氏布兰氏菌和金黄色葡萄球菌菌株引起的各种感染。头孢呋辛酯对肠杆菌科细菌有良好的活性,对非脆弱拟杆菌厌氧菌有中等的活性。临床研究表明,在治疗无并发症的尿路感染、急性中耳炎、上呼吸道感染、皮肤和软组织感染以及无并发症的淋病方面,它至少与氨苄西林、阿莫西林、阿莫西林/克拉维酸、青霉素V或头孢氯一样有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cefuroxime axetil.

Cefuroxime axetil is a orally active prodrug formulation of cefuroxime, which upon absorption undergoes immediate deesterification to free cefuroxime. Cefuroxime axetil offers an in vitro antibacterial spectrum against many gram-positive and some gram-negative organisms. Its beta-lactamase stability makes it useful in treating a variety of infections caused by beta-lactamase-producing strains of Haemophilus influenzae, Branhamella catarrhalis, and Staphylococcus aureus. Cefuroxime axetil has good activity against the Enterobacteriaceae and moderate activity against non-Bacteroides fragilis anaerobes. Clinical studies suggest it is at least as effective as ampicillin, amoxicillin, amoxicillin/clavulanic acid, penicillin V, or cefaclor in the treatment of uncomplicated urinary tract infections, acute otitis media, upper respiratory infections, skin and soft tissue infections, and uncomplicated gonorrhea.

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