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pubmed-article:14982803pubmed:abstractTextThe in vitro activities of tigecycline were tested against 831 isolates of the Bacteroides fragilis group representing all of the species within the group. On a weight-to-weight basis (8 microg/ml), tigecycline was more active than clindamycin, minocycline, trovafloxacin, and cefoxitin and less active than imipenem or piperacillin-tazobactam against all isolates of the B. fragilis group. Tigecycline geometric mean MICs were statistically higher against B. distasonis than other Bacteroides species (P value of 0.0001).lld:pubmed
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pubmed-article:14982803pubmed:dateRevised2009-11-18lld:pubmed
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pubmed-article:14982803pubmed:articleTitleIn vitro activities of tigecycline against the Bacteroides fragilis group.lld:pubmed
pubmed-article:14982803pubmed:affiliationDepartment of Medicine, Tufts-New England Medical Center, Boston, Massachusetts 02111, USA.lld:pubmed
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