1987
DOI: 10.2165/00003495-198734020-00002
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Cefmenoxime

Abstract: Cefmenoxime is an aminothiazolyl cephalosporin administered intravenously or intramuscularly. Like other 'third-generation' cephalosporins it is active in vitro against most common Gram-positive and Gram-negative pathogens, is a potent inhibitor of Enterobacteriaceae (including beta-lactamase-producing strains), and is resistant to hydrolysis by beta-lactamases. Cefmenoxime has a high rate of clinical efficacy in many types of infection and is at least equal in clinical and bacteriological efficacy to several … Show more

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Cited by 17 publications
(2 citation statements)
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“…Cipro oxacin inhibits bacterial DNA gyrase, making it a broad-spectrum antibacterial drug. It is highly susceptible to Gram-negative bacteria in vitro and moderately susceptible to Gram-positive bacteria [25]. The emergence of resistance to various classes of antibiotics can be linked to a number of factors, such as altered target-site architecture, altered cell membrane permeability, and e ux-pump mechanisms that lower antibiotic concentrations [26].…”
Section: Mic Of Aunps Cip and Cip @Au Nps Evaluationmentioning
confidence: 99%
“…Cipro oxacin inhibits bacterial DNA gyrase, making it a broad-spectrum antibacterial drug. It is highly susceptible to Gram-negative bacteria in vitro and moderately susceptible to Gram-positive bacteria [25]. The emergence of resistance to various classes of antibiotics can be linked to a number of factors, such as altered target-site architecture, altered cell membrane permeability, and e ux-pump mechanisms that lower antibiotic concentrations [26].…”
Section: Mic Of Aunps Cip and Cip @Au Nps Evaluationmentioning
confidence: 99%
“…Other examples exist, e. g . Azathioprine as immunosuppressant, [9,10] Triclabendazole [11] as an anti‐parasitic drug and Cefmenoxime as a third‐generation cephalosporin antibiotic [12] …”
Section: Figurementioning
confidence: 99%