Abstract
The in vitro activities of moxalactam, GR 20263 and N-formimidoyl thienamycin were compared to those of cephalothin, cefazolin, cefamandole, cefoxitin and tobramycin against 152 strains of Enterobacteriaceae and staphylococci. Moxalactam, GR 20263 and N-formimidoyl thienamycin each had significantly improved activity toward the gram-negative organisms tested compared to the other .beta.-lactams and tobramycin. N-formimidoyl thienamycin was particularly impressive with respect to its activity toward Staphylococcus aureus and S. epidermidis as compared to moxalactam, GR 20263 and the older .beta.-lactam drugs.