III. Indications

  1. Respiratory tract infections
  2. Acute Sinusitis
  3. Otitis Media

IV. Preparations

  1. Loracarbef (Lorabid)
    1. Adult: 200 to 400 mg po bid
    2. Child
      1. Otitis Media: 30 mg/kg/day divided bid
      2. Other infections: 15 mg/kg/day divided bid
    3. Directions
      1. Take more than 1 hour before or 2 hours after food
  2. Cefprozil (Cefzil)
    1. Adult: 250 to 500 mg PO divided qd to bid
    2. Child
      1. Otitis Media: 15 mg/kg/dose PO bid
      2. Pharyngitis: 7.5 mg/kg/dose PO bid for 10 days
  3. Cefuroxime (Ceftin, Zinacef)
    1. Adult
      1. Parenteral: 750 to 1500 mg IM or IV every 8 hours
      2. Oral: 250 to 500 mg PO bid
    2. Child
      1. Parenteral: 50-100 mg/kg/day IV divided q6-8 hours
      2. Oral: 20-30 mg/kg/day PO divided bid
        1. Reported to have unpleasant taste
    3. Directions
      1. Take with food
  4. Cefaclor (Ceclor)
    1. Listed for historical reference only
    2. Risk of significant serum-sickness type reaction

Images: Related links to external sites (from Google)

Cost: Medications

Cefuroxime Axetil (on 2/9/2012 at DrugStore.com)
Cefuroxime Axetil 250mg Tablets #20 for $73.99 ($3.70/unit)
Cefuroxime Axetil 500mg Tablets #20 for $98.99 ($4.95/unit)
Cefprozil (on 2/9/2012 at DrugStore.com)
Cefprozil 500mg Tablets #50 for $350.99 ($7.02/unit)
Cefzil (on 2/9/2012 at DrugStore.com)
Cefzil 250mg/5ml Suspension 50ml Bottle #1 for $45.99 ($45.99/unit)
Cefzil 250mg/5ml Suspension 100ml Bottle #1 for $73.99 ($73.99/unit)
Cefzil 250mg Tablets #20 for $109.99 ($5.50/unit)
Ceftin (on 2/9/2012 at DrugStore.com)
Ceftin 250mg Tablets #20 for $213.98 ($10.70/unit)
Ceftin 500mg Tablets #20 for $359.97 ($18.00/unit)

Ontology: Cefuroxime (C0007562)

Definition (NCI) A semisynthetic, broad-spectrum, beta-lactamase-resistant, second-generation cephalosporin with antibacterial activity. Cefuroxime binds to and inactivates penicillin-binding proteins (PBPs) located on the inner membrane of the bacterial cell wall. 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.
Definition (MSH) Broad-spectrum cephalosporin antibiotic resistant to beta-lactamase. It has been proposed for infections with gram-negative and gram-positive organisms, GONORRHEA, and HAEMOPHILUS.
Concepts Organic Chemical (T109) , Antibiotic(T195)
MSH D002444
SnomedCT 372833007, 73986003
English Cefuroxime, Cephuroxime, 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-, (6R-(6alpha,7beta(Z)))-, cefuroxime (medication), cefuroxime, Cefuroxime [Chemical/Ingredient], CEFUROXIME, cephuroxime, Cefuroxime (product), Cefuroxime (substance)
Swedish Cefuroxim
Czech cefuroxim
Finnish Kefuroksiimi
Russian TSEFUROKSIM, ЦЕФУРОКСИМ
Japanese セフロキシム
Croatian CEFUROKSIM
Polish Cefuroksym
Spanish cefuroxima (producto), cefuroxima (sustancia), cefuroxima, Cefuroxima
French Céfuroxime
German Cefuroxim
Italian Cefuroxima
Portuguese Cefuroxima

Ontology: cefprozil (C0053882)

Definition (NCI) 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.
Concepts Organic Chemical (T109) , Antibiotic(T195)
MSH C052018
SnomedCT 387538005, 96054007
English cefprozil, CEFPROZIL, cefprozil (medication), 5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 7-(((2R)-amino(4-hydroxyphenyl)acetyl)amino)-8-oxo-3-(1-propenyl)-, (6R,7R)-, cefprozil [Chemical/Ingredient], Cefprozil, Cefprozil (product), Cefprozil (substance)
Spanish cefprozilo (producto), cefprozilo, cefprozilo (sustancia), cefprozil, cefprozil (producto), cefprozil (sustancia)

Ontology: loracarbef (C0065295)

Definition (NCI) A semi-synthetic, broad-spectrum, beta-lactamase resistant, second-generation cephalosporin antibiotic derived from cephasporium. The bactericidal activity of loracarbef results from the inhibition of bacterial cell wall synthesis through interference with the cross-linking of peptidoglycan units. This results in a reduction of cell wall stability and causes cell lysis. Loracarbef is more active against a variety of gram-negative organisms but less active against gram-positive pathogens compared to first-generation agents.
Concepts Organic Chemical (T109) , Antibiotic(T195)
MSH C054920
SnomedCT 96061006, 370362008
English 1-Azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 7-((aminophenylacetyl)amino)-3-chloro-8-oxo-, (6R-(6alpha,7beta(R*)))-, loracarbef, (6R, 7S)-7-[(R)-2-Amino-2-phenylacetamido]-3-chloro-8-oxo-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid, Monohydrate, loracarbef (medication), loracarbef [Chemical/Ingredient], Carbacefaclor, Loracarbef, Loracarbef (substance), Loracarbef product (product), Loracarbef product, LORACARBEF
Spanish loracarbef, producto con loracarbef (producto), loracarbef (producto), producto con loracarbef, carbacefaclor (sustancia), carbacefaclor

Ontology: Ceftin (C0719197)

Concepts Organic Chemical (T109) , Antibiotic(T195)
MSH C040738
English Ceftin, ceftin

Ontology: Lorabid (C0721422)

Concepts Organic Chemical (T109) , Antibiotic(T195)
MSH C054920
English lorabid, Lilly Brand of Loracarbef Monohydrate, Monarch Brand of Loracarbef Monohydrate, Lorabid

Ontology: Cefzil (C0728743)

Concepts Organic Chemical (T109) , Antibiotic(T195)
MSH C052018
English Cefzil, cefzil, Bristol-Myers Squibb brand of cefprozil