INVITRO ACTIVITY OF BAY V-3522, A NEW ORAL CEPHALOSPORIN

被引:3
|
作者
FASS, RJ
机构
[1] Division Infectious Diseases, Department Internal Medicine, Ohio State Univ. College Med., Columbus
关键词
D O I
10.1128/AAC.34.9.1855
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The in vitro activity of BAY v 3522 was compared with the activities of cephalexin, cefaclor, cefuroxime, cefixime, and amoxicillin-clavulanate. MICs (in μg/ml) of BAY v 3522 were as follows: Staphylococcus spp. (except for oxacillin-resistant strains), 0.13 to 1; Streptococcus spp. (except for some viridans group streptococci), ≤ 0.015 to 0.25; Enterococcus faecalis, 2 to 8; other enterococci, 0.5 to > 32; β-lactamase-negative Haemophilus influenzae and Branhamella catarrhalis, 0.13 to 1; β-lactamase-positive H. influenzae and B. catarrhalis, 0.5 to 4; Pasteurella multocida, 0.06 to 0.25; and members of the family Enterobacteriaceae, 0.5 to < 32. Among the cephalosporins, BAY v 3522 was the most active against gram-positive cocci and cefixime was the most active against gram-negative bacilli; BAY v 3522 was similar in activity to amoxicillin-clavulanate against most species.
引用
收藏
页码:1855 / 1857
页数:3
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