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Clin Infect Dis. 2012;54:e132–73.PubMedCrossRef 39. Bushby SR. Trimethoprim–sulfamethoxazole: in vitro

microbiological aspects. J Infect Dis. 1973;128 Suppl:442 (p 462).CrossRef 40. Trickett PC, Dineen P, Mogabgab W. Clinical experience: respiratory tract. Trimethoprim–sulfamethoxazole versus penicillin G in the treatment of group A beta-hemolytic streptococcal pharyngitis and tonsillitis. J Infect Dis. 1973;128 Suppl:693 (p 695).CrossRef 41. Kaplan EL, Johnson DR, Del Rosario MC, Horn DL. Susceptibility of group A beta-hemolytic streptococci to thirteen Selleckchem Napabucasin antibiotics: examination of 301 strains isolated in the United States between 1994 and 1997. Pediatr Infect Dis J. 1999;18:1069–72.PubMedCrossRef 42. Bowen AC, Lilliebridge RA, Tong SY, et al. Is Streptococcus pyogenes resistant or susceptible to trimethoprim–sulfamethoxazole? J Clin Microbiol. 2012;50:4067–72.PubMedCentralPubMedCrossRef 43. Current practice guidelines for management of SSTI’s; 2005. http://​cid.​oxfordjournals.​org/​content/​41/​10/​1373/​F3.​expansion.​html. Accessed Oct 24, 2013.”
“Introduction Several authorities have

GSK1120212 called attention to the morbidity, mortality and excess health costs associated with antibiotic-resistant pathogens and the need to prioritize development of antibacterial agents that can safely and effectively treat these pathogens [1–4]. Ceftaroline fosamil is a novel cephalosporin, with bactericidal in vitro activity against pathogens associated with licensed indications, including resistant organisms, such as methicillin-resistant Staphylococcus aureus (MRSA), multidrug-resistant Streptococcus

pneumoniae (MDRSP) and penicillin-resistant S. pneumoniae (PRSP) [5]. Supported by preclinical in vitro and animal model studies [6–10] and clinical trials [11–15], ceftaroline fosamil (Teflaro™; Forest Laboratories, Inc., New York, USA) was approved by the United States Food and Drug Administration (FDA) in October 2010 for the treatment of adults with community-acquired bacterial pneumonia (CABP) and acute bacterial skin and skin structure infections (ABSSSI) caused by susceptible organisms Sitaxentan [5]. Ceftaroline fosamil is the newest of only three systemic antibiotics approved for human use by the FDA over the past 5 years and the only one of these approved for the treatment of CABP. Similarly, the European Commission granted marketing authorization for ceftaroline fosamil (Zinforo™; AstraZeneca, Södertälje, Sweden) in August 2012 for the treatment of community-acquired pneumonia and complicated skin and soft tissue infections following favorable opinion from the Committee for Medicinal Products for Human Use [16]. This report reviews the recent literature published on ceftaroline fosamil, including the pivotal clinical trials that led to its approval, and highlights areas that need to be addressed in the future.

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  2. g , Maya, Turner and Sabloff, 2012; Chaco Canyon, English
  3. 9 Our patient recounted only a single 3-day visit to an endemic a
  4. Stem Cells 2008,26(6):1414–1424 PubMedCrossRef 12 Chung LW, Base
  5. 2012 Aug 1;123(4):225–239 2  Lubel JS ,
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