Enterococcal Superinfection and Colonization After Therapy with Moxalactam, a New Broad-Spectrum Antibiotic

  1. VICTOR L. YU, M.D.
  1. University of Pittsburgh School of Medicine and Veterans Administration Medical Center;
    Pittsburgh, Pennsylvania

    Excerpt

    Moxalactam is a new broad-spectrum antimicrobial drug that is structurally related to the cephalosporins (1). Its favorable pharmacokinetic properties allow it to be administered at 8-hour intervals (2), and unlike other cephalosporins, it reaches the cerebrospinal fluid in therapeutic concentrations (3). However, its major attraction is its effectiveness in vitro against many bacterial pathogens. It is active against the usual pathogenic gram-positive cocci (streptococci, pneumococci, staphylococci) as well as the Enterobacteriaceae (1, 4). Moreover, it is active in vitro against anaerobes (including Bacteroides fragilis) as well as Haemophilus influenzae (including ampicillin-resistant strains) and Pseudomonas aeruginosa (4-6). No other commercially available

    This 100-word excerpt has been provided in the absence of an abstract.

    Article and Author Information

    • ▸Requests for reprints should be addressed to Victor L. Yu, M.D.; Department of Medicine, University of Pittsburgh School of Medicine, 968 Scaife Hall; Pittsburgh, PA 15261.

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