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1 biotics containing hydrolyzed cefotaxime and faropenem.
3 ability of a disc susceptibility test using faropenem (10 mug) to predict carbapenemase activity in
4 ng the CLSI/EUCAST methodology with discs of faropenem (10 mug), temocillin (30 mug), and four carbap
5 nd 43.9% for temocillin, 57.1% and 98.8% for faropenem, 53.6% and 100% for the OXA-48 disk test, 98.8
6 s, a new algorithm incorporating temocillin, faropenem, and ICT which allows cost-effective detection
7 99% showed growth up to the edge of a 10-mug faropenem disc compared with only 6% of other beta-lacta
8 reference laboratory, growth up to a 10-mug faropenem disc correctly identified 84 of 86 carbapenema
11 Four phenotypic tests (temocillin disk test, faropenem disk test, OXA-48 disk test, and high-inoculum
13 en and doses of linezolid, moxifloxacin, and faropenem identified are proposed to be adequate for all
16 were AUC0-24/MIC ratios of 62 and 122, and a faropenem percentage of time above MIC >60%, in combinat
17 First, we varied the percentage of time that faropenem persisted above minimum inhibitory concentrati
18 e oral doses of linezolid, moxifloxacin, and faropenem that would achieve optimal target exposures as
19 of standard linezolid and moxifloxacin plus faropenem TMIC > 60%, as well as higher-dose moxifloxaci
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