What we found on the web about Ceftobiprole
Ceftobiprole (Zeftera / Zevtera) is a next generation (5th generation) cephalosporin antibiotic with activity against methicillin-resistant Staphylococcus aureus, penicillin ...
Ceftobiprole has been described as "fifth generation", [14] [15] though acceptance for this terminology is not universal. Ceftobiprole (and the soluble prodrug medocaril) are on the FDA ...
1: Diagn Microbiol Infect Dis. 2007 Dec;59(4):463-6. Epub 2007 Oct 29. Activity of ceftobiprole against community-associated methicillin-resistant Staphylococcus aureus isolates ...
Johnson & Johnson Pharmaceutical Research & Development, L.L.C., announced that the investigational antibiotic ceftobiprole was as effective as commonly used combination therapy ...
1: Clin Infect Dis. 2008 Mar 1;46(5):656-8. Comment on: Clin Infect Dis. 2008 Mar 1;46(5):647-55. Ceftobiprole: a new option for treatment of skin and soft-tissue infections due to ...
The company`s diversified portfolio includes two commercialized drugs (alitretinoin, ceftobiprole), one investigational drug in phase III (isavuconazole) as well as innovative ...
A Johnson & Johnson unit has filed for Swiss approval to sell ceftobiprole, marketed in partnership with developer Basilea Pharmaceutical, as a treatment for diabetic foot ...
Ceftobiprole is the first anti-MRSA broad-spectrum cephalosporin to demonstrate efficacy in a large clinical trial in patients infected with staphylococcal infections, including ...
Ceftobiprole belongs to a well accepted class of antibacterial agents known as cephalosporins that are used to treat serious life-threatening infections caused by Gram ...
Sponsor: Johnson & Johnson Pharmaceutical Research & Development, L.L.C. Information provided by: Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
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Ceftobiprole (Zeftera/Zevtera) is a next generation (5th generation) cephalosporin antibiotic with activity against methicillin-resistant Staphylococcus aureus, penicillin-resistant Streptococcus pneumoniae, Pseudomonas aeruginosa, and Enterococci. It was discovered by Basilea Pharmaceutica and was developed by Johnson & Johnson Pharmaceutical Research and Development. It has been shown to be statistically non-inferior to the combination of vancomycin and ceftazidime for the treatment of skin and soft tissue infections.

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