- 1. CEF
- (UMLS (NCI) C0060133) =Therapeutic or Preventive Procedure ;
| - 18. CEFOTETAN
- [A semi-synthetic, broad-spectrum, beta-lactamase-resistant, second-generation cephalosporin antibiotic derived from cephalosporium. The bactericidal activity of cefotetan disodium is caused by an inhibition of bacterial cell wall synthesis via inhibition of cross-linking of peptidoglycans. This results in a reduction of cell wall stability and causes cell lysis. Cefotetan disodium is more active against gram-negative organisms and less active against gram-positive organisms compared to first-generation cephalosporins. ( NCI )] (UMLS (NCI) C0007555) =Organic Chemical; Antibiotic =Tetrazoles;
Cephalosporanic Acids;
[AM102] CEPHALOSPORINS, 2ND GENERATION;
=5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 7-(((4-(2-amino-1-carboxy-2-oxoethylidene)-1,3-dithietan-2-yl)carbonyl)amino)-7-methoxy-3-(((1-methyl-1H-tetrazol-5-yl)thio)methyl)-8-oxo-, Disodium Salt,(6R-(6alpha,7alpha))- |
- 2. CEFACLOR
- [A beta-lactam, second-generation cephalosporin antibiotic with bactericidal activity. Cefaclor binds to and inactivates penicillin-binding proteins (PBP) located in bacterial cytoplasmic membranes. PBPs are enzymes involved in the terminal stages of assembling the bacterial cell wall and in reshaping the cell wall during growth and division. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. This results in the weakening of the bacterial cell wall and causes cell lysis. ( NCI )] (UMLS (NCI) C0007537) =Organic Chemical; Antibiotic =cephalexin;
[AM102] CEPHALOSPORINS, 2ND GENERATION =CEFACLOR MONOHYDRATE;
CEFACLOR 250 MG;
CEFACLOR 187 MG/5ML;
CEFACLOR 375 MG;
CEFACLOR 500 MG;
CEFACLOR 375 MG/5ML;
CEFACLOR 125 MG/5ML;
CEFACLOR 250 MG/5ML;
| - 19. CEFOTIAM
- [One of the CEPHALOSPORINS that has a broad spectrum of activity against both gram-positive and gram-negative microorganisms. ( MSH )] (UMLS (NCI) C0007556) =Organic Chemical; Antibiotic
|
- 3. Cefadyl
- (UMLS (NCI) C0733791) =Organic Chemical; Antibiotic ;
| - 20. CEFOTIAM HYDROCHLORIDE
- (UMLS (NCI) C0771454) =Organic Chemical; Antibiotic
|
- 4. Cefamandole Nafate
- [The sodium salt form of cefamandole formyl ester. Cefamandole nafate is a pro-drug that is hydrolyzed by plasma esterases to produce cefamandole, a semi-synthetic beta-lactam, second-generation cephalosporin antibiotic with bactericidal activity. Cefamandole binds to and inactivates 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. This results in the weakening of the bacterial cell wall and causes cell lysis. ( NCI )] (UMLS (NCI) C0054995) =Organic Chemical; Antibiotic ;
=(6R,7R)-7-(R)-Mandelamido-3-(((1-methyl-1H-tetrazol-5-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-carboxylic Acid;
=CEFAMANDOLE NAFATE 1 GM;
CEFAMANDOLE NAFATE 1 GM/VIL;
CEFAMANDOLE NAFATE 2 GM/VIL;
CEFAMANDOLE NAFATE 2 GM | - 21. CEFOXITIN
- [A semisynthetic cephamycin antibiotic resistant to beta-lactamase. ( MSH )] (UMLS (NCI) C0007557) =Organic Chemical; Antibiotic =Cephalosporanic Acids;
[AM102] CEPHALOSPORINS, 2ND GENERATION =CEFOXITIN SODIUM |
- 5. Cefdinir
- [A semi-synthetic cephalosporin and a beta-lactam antibiotic with bactericidal activity. Cefdinir's effect is dependent on its binding to penicillin-binding proteins (PBPs) located in the bacterial cytoplasmic membrane. Binding results in the inhibition of the transpeptidase enzymes, thereby preventing cross-linking of the pentaglycine bridge with the fourth residue of the pentapeptide and interrupting consequent synthesis of peptidoglycan chains. As a result, cefdinir inhibits bacterial septum and cell wall synthesis formation. ( NCI )] (UMLS (NCI) C0060405) =Organic Chemical; Antibiotic =[AM103] CEPHALOSPORINS, 3RD GENERATION;
Unclassified Ingredients =CEFDINIR 125 MG/5ML;
CEFDINIR 300 MG | - 22. Cefpiramide
- (UMLS (NCI) C0055010) =Organic Chemical; Pharmacologic Substance ;
|
- 6. Cefepime
- [A drug used to treat infection. It belongs to the family of drugs called cephalosporin antibiotics. ( NCI )] (UMLS (NCI) C0055003) =Organic Chemical; Antibiotic ;
=[AM104] CEPHALOSPORINS, 4TH GENERATION;
Unclassified Ingredients =Cefepime Hydrochloride;
| - 23. CEFPIRAMIDE SODIUM
- (UMLS (NCI) C0955901) =Organic Chemical; Antibiotic
|
- 7. 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 =Cefepime;
=CEFEPIME HYDROCHLORIDE 1 GM;
CEFEPIME HYDROCHLORIDE 2 GM;
CEFEPIME HYDROCHLORIDE 500 MG;
| - 24. Cefpodoxime
- [A third generation semi-synthetic cephalosporin and a beta-lactam antibiotic with bactericidal activity. Cefpodoxime's effect is dependent on its binding to penicillin-binding proteins (PBPs) located in the bacterial cytoplasmic membrane. Binding results in the inhibition of the transpeptidase enzymes, thereby preventing cross-linking of the pentaglycine bridge with the fourth residue of the pentapeptide and interrupting consequent synthesis of peptidoglycan chains. As a result, cefpodoxime inhibits bacterial septum and cell wall synthesis formation. ( NCI )] (UMLS (NCI) C0055011) =Organic Chemical; Antibiotic ;
=[AM103] CEPHALOSPORINS, 3RD GENERATION;
=Cefpodoxime Proxetil;
|
- 8. CEFIXIME
- [A broad-spectrum, third-generation cephalosporin antibiotic derived semisynthetically from the marine fungus Cephalosporium acremonium with antibacterial activity. As does penicillin, the beta-lactam antibiotic cefixime inhibits bacterial cell wall synthesis by disrupting peptidoglycan synthesis, resulting in a reduction in bacterial cell wall stability and bacterial cell lysis. Stable in the presence of a variety of beta-lactamases, this agent is more active against gram-negative bacteria and less active against gram-positive bacteria compared to second-generation cephalosporins. ( NCI )] (UMLS (NCI) C0060400) =Organic Chemical; Antibiotic =CEFOTAXIME;
[AM103] CEPHALOSPORINS, 3RD GENERATION =CEFIXIME 100 MG/5ML;
CEFIXIME 200 MG;
CEFIXIME 400 MG;
| - 25. Cefpodoxime Proxetil
- [A third generation semi-synthetic cephalosporin and a beta-lactam antibiotic with bactericidal activity. Cefpodoxime's effect is dependent on its binding to penicillin-binding proteins (PBPs) located in the bacterial cytoplasmic membrane. Binding results in the inhibition of the transpeptidase enzymes, thereby preventing cross-linking of the pentaglycine bridge with the fourth residue of the pentapeptide and interrupting consequent synthesis of peptidoglycan chains. As a result, cefpodoxime inhibits bacterial septum and cell wall synthesis formation. ( NCI )] (UMLS (NCI) C0108938) =Organic Chemical; Antibiotic ;
=CEFTIZOXIME;
Cefpodoxime =CEFPODOXIME PROXETIL 100 MG;
CEFPODOXIME PROXETIL 200 MG;
CEFPODOXIME PROXETIL 100 MG/5ML;
CEFPODOXIME PROXETIL 50 MG/5ML;
|
- 9. Cefizox
- (UMLS (NCI) C0701023) =Organic Chemical; Antibiotic ;
| - 26. Cefprozil
- [A semi-synthetic cephalosporin and a beta-lactam antibiotic with bactericidal activity. Cefprozil's effect is dependent on its binding to penicillin-binding proteins (PBPs) located in the bacterial cytoplasmic membrane. Binding results in the inhibition of the transpeptidase enzymes, thereby preventing cross-linking of the pentaglycine bridge with the fourth residue of the pentapeptide and interrupting consequent synthesis of peptidoglycan chains. As a result, cefprozil inhibits bacterial septum and cell wall synthesis formation. ( NCI )] (UMLS (NCI) C0053882) =Organic Chemical; Antibiotic ;
=[AM102] CEPHALOSPORINS, 2ND GENERATION;
Unclassified Ingredients =CEFPROZIL 250 MG;
CEFPROZIL 250 MG/5ML;
CEFPROZIL 500 MG;
CEFPROZIL 125 MG/5ML;
|
- 10. CEFMENOXIME
- [A cephalosporin antibiotic that is administered intravenously or intramuscularly. It is active against most common gram-positive and gram-negative microorganisms, is a potent inhibitor of Enterobacteriaceae, and is highly resistant to hydrolysis by beta-lactamases. The drug has a high rate of efficacy in many types of infection and to date no severe side effects have been noted. ( MSH )] (UMLS (NCI) C0007549) =Organic Chemical; Antibiotic
| - 27. CEFTAZIDIME
- [A beta-lactam, third-generation cephalosporin antibiotic with bactericidal activity. Ceftazidime binds to and inactivates penicillin-binding proteins (PBP) located on the inner membrane of the bacterial cell wall. PBPs participate in the terminal stages of assembling the bacterial cell wall, and in reshaping the cell wall during cell division. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. This results in the weakening of the bacterial cell wall and causes cell lysis. Compared to the second and first generation cephalosporins, ceftazidime is more active against gram-negative bacteria and less active against gram-positive bacteria. Ceftazidine also crosses the blood-brain barrier and reaches therapeutic concentrations in the central nervous system (CNS). ( NCI )] (UMLS (NCI) C0007559) =Organic Chemical; Antibiotic =Cephaloridine;
[AM103] CEPHALOSPORINS, 3RD GENERATION =CEFTAZIDIME 1 GM/50ML;
CEFTAZIDIME 2 GM/50ML;
CEFTAZIDIME 1 GM;
CEFTAZIDIME 500 MG;
CEFTAZIDIME 2 GM/VIL;
CEFTAZIDIME 6 GM/VIL;
CEFTAZIDIME 10 GM;
CEFTAZIDIME 1 GM/VIL;
CEFTAZIDIME 2 GM |
- 11. CEFMENOXIME HYDROCHLORIDE
- (UMLS (NCI) C0282390) =Organic Chemical; Antibiotic ;
| - 28. Ceftazidime Sodium
- [A beta-lactam, third-generation cephalosporin antibiotic with bactericidal activity. Ceftazidime binds to and inactivates penicillin-binding proteins (PBP) located on the inner membrane of the bacterial cell wall. PBPs participate in the terminal stages of assembling the bacterial cell wall, and in reshaping the cell wall during cell division. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. This results in the weakening of the bacterial cell wall and causes cell lysis. Compared to the second and first generation cephalosporins, ceftazidime is more active against gram-negative bacteria and less active against gram-positive bacteria. Ceftazidine also crosses the blood-brain barrier and reaches therapeutic concentrations in the central nervous system (CNS). ( NCI )] (UMLS (NCI) C0724548) =Organic Chemical; Antibiotic ;
|
- 12. CEFMETAZOLE
- [A semisynthetic cephamycin antibiotic with a broad spectrum of activity against both gram-positive and gram-negative microorganisms. It has a high rate of efficacy in many types of infection and to date no severe side effects have been noted. ( MSH )] (UMLS (NCI) C0007550) =Organic Chemical; Antibiotic =Cephalosporanic Acids;
[AM102] CEPHALOSPORINS, 2ND GENERATION;
TO BE DELETED INGREDIENT PREPARATIONS;
=CEFMETAZOLE SODIUM | - 29. Ceftibuten Dihydrate
- (UMLS (NCI) C0873024) CEFTIBUTEN DIHYDRATE PREPARATION;
=Organic Chemical; Pharmacologic Substance ;
=CEFTIBUTEN;
=CEFTIBUTEN DIHYDRATE 400 MG;
CEFTIBUTEN DIHYDRATE 90 MG/5ML;
CEFTIBUTEN DIHYDRATE 180 MG/5ML |
- 13. Cefobid
- (UMLS (NCI) C0733366) =Organic Chemical; Antibiotic ;
| - 30. CEFTIZOXIME
- [A semisynthetic cephalosporin antibiotic which can be administered intravenously or by suppository. The drug is highly resistant to a broad spectrum of beta-lactamases and is active against a wide range of both aerobic and anaerobic gram-positive and gram-negative organisms. It has few side effects and is reported to be safe and effective in aged patients and in patients with hematologic disorders. ( MSH )] (UMLS (NCI) C0007560) =Organic Chemical; Antibiotic =CEFOTAXIME;
[AM103] CEPHALOSPORINS, 3RD GENERATION =Cefpodoxime Proxetil;
5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic Acid, 7-(((2,3-dihydro-2-imino-4-thiazolyl)(methoxyimino)acetyl)amino)-8-oxomonosodium Salt,(6R-(6alpha,7beta(Z)))-;
|
- 14. CEFONICID
- [A second-generation cephalosporin administered intravenously or intramuscularly. Its bactericidal action results from inhibition of cell wall synthesis. It is used for urinary tract infections, lower respiratory tract infections, and soft tissue and bone infections. ( MSH )] (UMLS (NCI) C0007551) =Organic Chemical; Antibiotic =Cephalosporanic Acids;
[AM102] CEPHALOSPORINS, 2ND GENERATION;
TO BE DELETED INGREDIENT PREPARATIONS;
=Cefonicid Monosodium | - 31. Ceftobiprole
- (UMLS (NCI) C1100584) =Organic Chemical; Pharmacologic Substance
|
- 15. CEFOPERAZONE
- [Semisynthetic broad-spectrum cephalosporin with a tetrazolyl moiety that is resistant to beta-lactamase. It has been proposed especially against Pseudomonas infections. ( MSH )] (UMLS (NCI) C0007552) =Organic Chemical; Antibiotic =(6R,7R)-7-(R)-Mandelamido-3-(((1-methyl-1H-tetrazol-5-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-carboxylic Acid;
[AM103] CEPHALOSPORINS, 3RD GENERATION =CEFOPERAZONE SODIUM | - 32. CEFTRIAXONE
- [An antibiotic drug used to treat infection. It belongs to the family of drugs called cephalosporin antibiotics. ( NCI )] (UMLS (NCI) C0007561) =Organic Chemical; Antibiotic =CEFOTAXIME;
[AM103] CEPHALOSPORINS, 3RD GENERATION =CEFTRIAXONE SODIUM |
- 16. Cefotan
- (UMLS (NCI) C0007553) =Organic Chemical; Antibiotic
| - 33. ceftrixone
- [ ] (UMLS (CSP) C0597871) =Organic Chemical; Pharmacologic Substance
|
- 17. CEFOTAXIME
- [A third generation semisynthetic cephalosporin antibiotic with bactericidal activity. Cefotaxime inhibits mucopeptide synthesis by binding to and inactivating penicillin binding proteins thereby interfering with the final transpeptidation step required for cross-linking of peptidoglycan units which are a component of bacterial cell walls. This results in a reduction of cell wall stability and causes cell lysis. ( NCI )] (UMLS (NCI) C0007554) =Organic Chemical; Antibiotic =Cephacetrile;
[AM103] CEPHALOSPORINS, 3RD GENERATION =CEFTIZOXIME;
CEFTRIAXONE;
CEFUROXIME;
CEFIXIME;
CEFOTAXIME SODIUM | - 34. Cefuroxime Axetil
- [A second generation semi-synthetic cephalosporin and a beta-lactam antibiotic with bactericidal activity. Cefuroxime's effect is dependent on its binding to penicillin-binding proteins (PBPs) located in the bacterial cytoplasmic membrane. Binding results in the inhibition of the transpeptidase enzymes, thereby preventing cross-linking of the pentaglycine bridge with the fourth residue of the pentapeptide and interrupting consequent synthesis of peptidoglycan chains. As a result, cefuroxime inhibits bacterial septum and cell wall synthesis formation. ( NCI )] (UMLS (NCI) C0055015) =Organic Chemical; Antibiotic ;
=CEFUROXIME;
=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)))-;
CEFUROXIME AXETIL 125 MG/5ML;
CEFUROXIME AXETIL 125 MG;
CEFUROXIME AXETIL 250 MG;
CEFUROXIME AXETIL 500 MG;
CEFUROXIME AXETIL 250 MG/5ML |
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