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
T T T, T- T0 T1 T2 T3 T4 T9 TA TB TC TD TE TF TG TH TI TJ TK TL TM TN TO TP TQ TR TS TT TU TV TW TY TZ
TH TH2 THA THB THC THE THI THL THO THP THR THU THY

5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic Acid, 3-(((aminocarbonyl)oxy)methyl)-7-((2-furanyl(methoxyimino)acetyl)amino)-8-oxo-, Monosodium Salt(6R-(6alpha,7beta(Z)))-

[The sodium salt form of cefuroxime and a semi-synthetic, broad-spectrum, beta-lactamase resistant, second-generation cephalosporin antibiotic with bactericidal activity. Cefuroxime sodium inhibits bacterial cell wall synthesis by inactivating penicillin binding proteins (PBPs) thereby interfering with the final transpeptidation step required for cross-linking of peptidoglycan units which are a component of the cell wall. Lack of cross-linking results in a reduction of cell wall stability and leads to cell lysis. ( NCI )]
UMLS (NCI) C0701852
 
Organic Chemical
Antibiotic
Relation/PAR: CEFUROXIME
Cefuroxime Axetil
Relation/CHD: Cefuroxime 1.5 MG/ML Injectable Solution
CEFUROXIME SODIUM 7.5 GM/VIL
CEFUROXIME SODIUM 30 MG/ML
CEFUROXIME SODIUM 15 MG/ML
CEFUROXIME SODIUM 7.5 MG/ML
CEFUROXIME SODIUM 7.5 GM
CEFUROXIME SODIUM 750 MG

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