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dc.contributor.authorTansino, G F
dc.contributor.authorHammerschlag, M R
dc.contributor.authorCongeni, B L
dc.contributor.authorCox, P A
dc.contributor.authorDoraiswamy, B
dc.contributor.authorduBouchet, L
dc.date.accessioned2023-06-02T15:43:19Z
dc.date.available2023-06-02T15:43:19Z
dc.date.issued1985-10
dc.identifier.citationTansino GF, Hammerschlag MR, Congeni BL, Cox PA, Doraiswamy B, duBouchet L. Clinical efficacy and safety of cefmenoxime in children. Antimicrob Agents Chemother. 1985 Oct;28(4):508-10. doi: 10.1128/AAC.28.4.508. PMID: 3865630; PMCID: PMC180293.en_US
dc.identifier.issn0066-4804
dc.identifier.pmid3865630
dc.identifier.urihttp://hdl.handle.net/20.500.12648/8875
dc.description.abstractCefmenoxime, an investigational semisynthetic cephalosporin, was evaluated in 18 pediatric patients with a variety of infections. There were seven patients with urinary tract infections, two with wound infections, two with osteomyelitis, two with abscess infections, one with cervical adenitis, one with hidradenitis, one with pneumonia and sepsis, one with periorbital cellulitis, and one with ventriculitis. A total of 16 (88%) patients had a satisfactory clinical response demonstrated by improvement in clinical signs and symptoms. A total of 12 (67%) patients demonstrated eradication of their infecting organisms. Of the pathogens isolated in these patients, 16 isolates were susceptible to cefmenoxime. One patient developed a generalized urticarial rash that resolved within 24 h after cessation of cefmenoxime therapy. Mean peak level in serum after intravenous infusion was 55 micrograms/ml.
dc.language.isoenen_US
dc.relation.urlhttps://journals.asm.org/doi/10.1128/AAC.28.4.508en_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleClinical efficacy and safety of cefmenoxime in children.en_US
dc.typeArticle/Reviewen_US
dc.source.journaltitleAntimicrobial agents and chemotherapyen_US
dc.source.volume28
dc.source.issue4
dc.source.beginpage508
dc.source.endpage10
dc.source.countryUnited States
dc.description.versionVoRen_US
refterms.dateFOA2023-06-02T15:43:22Z
html.description.abstractCefmenoxime, an investigational semisynthetic cephalosporin, was evaluated in 18 pediatric patients with a variety of infections. There were seven patients with urinary tract infections, two with wound infections, two with osteomyelitis, two with abscess infections, one with cervical adenitis, one with hidradenitis, one with pneumonia and sepsis, one with periorbital cellulitis, and one with ventriculitis. A total of 16 (88%) patients had a satisfactory clinical response demonstrated by improvement in clinical signs and symptoms. A total of 12 (67%) patients demonstrated eradication of their infecting organisms. Of the pathogens isolated in these patients, 16 isolates were susceptible to cefmenoxime. One patient developed a generalized urticarial rash that resolved within 24 h after cessation of cefmenoxime therapy. Mean peak level in serum after intravenous infusion was 55 micrograms/ml.
dc.description.institutionSUNY Downstateen_US
dc.description.departmentPediatricsen_US
dc.description.degreelevelN/Aen_US
dc.identifier.journalAntimicrobial agents and chemotherapy


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