UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
C C- C1 C3 C5 C6 C7 CA CB CC CD CE CF CG CH CI CJ CK CL CM CN CO CP CQ CR CS CT CU CV CW CX CY CZ
CE CEA CEB CEC CED CEE CEF CEL CEM CEN CEP CER CES CET CEV

Cefepime Hydrochloride

[The hydrochoride salt of a semi-synthetic, beta-lactamase-resistant, fourth-generation cephalosporin antibiotic derived from an Acremonium fungal species with broad-spectrum bactericidal activity. Administered parenterally, cefipime inhibits bacterial cell wall synthesis by binding to and inactivating penicillin-binding proteins (PBP) located on the inner membrane of the bacterial cell wall. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity, resulting in a reduction of bacterial cell wall stability and cell lysis. This agent is more active against a variety of Gram-positive pathogens compared to third-generation cephalosporins. ( NCI )]
UMLS (NCI) C0771284
CEFEPIME HYDROCHLORIDE PREPARATION
 
Organic Chemical
Antibiotic
Relation/PAR: Cefepime
Relation/CHD: CEFEPIME HYDROCHLORIDE 1 GM
CEFEPIME HYDROCHLORIDE 2 GM
CEFEPIME HYDROCHLORIDE 500 MG

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