Cefpodoxime

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Structural formula
Structure of cefpodoxime
General
Non-proprietary name Cefpodoxime
other names

(6 R , 7 R ) -7 - {[(2 Z ) -2- (2-amino-1,3-thiazol-4-yl) -2-methoxyimino-acetyl] amino} -3- (methoxymethyl) - 8-oxo-5-thia-1-azabicyclo [4.2.0] oct-2-ene-2-carboxylic acid

Molecular formula C 15 H 17 N 5 O 6 S 2
External identifiers / databases
CAS number
  • 80210-62-4 (free acid)
  • 82619-04-3 (sodium salt)
EC number 685-334-0
ECHA InfoCard 100.210.871
PubChem 6335986
ChemSpider 4891496
DrugBank DB01416
Wikidata Q415173
Drug information
ATC code

J01 DD13

Drug class

β-lactam antibiotics
(3rd generation cephalosporins)

properties
Molar mass 427.458 g · mol -1
safety instructions
Please note the exemption from the labeling requirement for drugs, medical devices, cosmetics, food and animal feed
GHS hazard labeling
no classification available
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Cefpodoxime is an antibiotic from the group of third generation cephalosporins and is administered orally (oral cephalosporin).

application

Cefpodoxime is used to treat infections

It is also used as oral continuation therapy when intravenous cephalosporins are no longer necessary for sustained treatment. The antibiotic is also used in veterinary medicine.

It is recommended by the Paul Ehrlich Society as the drug of choice for the treatment of acute otitis media , acute sinusitis and the exacerbation of chronic bronchitis .

Spectrum of activity

Cefpodoxime is active against most gram-positive and gram-negative organisms.

Staphylococcus aureus ( methicillin- sensitive) is moderately to well sensitive . Other sensitive germs are Streptococcus pneumoniae , B-streptococci ( Streptococcus agalactiae ), Streptococcus pyogenes , Haemophilus influenzae , Moraxella catarrhalis , Escherichia coli , Klebsiella pneumoniae , Proteus mirabilis and other enterobacteria .

Pseudomonas aeruginosa , enterococci , Bacteroides fragilis and Proteus vulgaris , for example, are naturally resistant . Some germs can be insensitive to cefpodoxime due to an acquired antibiotic resistance, e.g. Morganella morganii , Citrobacter spp. and Enterobacter spp.

application

Cefpodoxime is administered orally as a prodrug variant of cefpodoxime proxetil .

Individual evidence

  1. This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
  2. H. Scholz, F. Vogel, Marianne Abele-Horn, D. Adam and others: Rational use of oral antibiotics in children and adolescents. Recommendations of an expert commission of the Paul Ehrlich Society for Chemotherapy e. V. In: Chemotherapy Journal. 11, 2002, pp. 59-70.
  3. F. Vogel, H. Scholz, B. Al-Nawas, W. Elies and others: Rational use of oral antibiotics in adults. Recommendations of an expert commission of the Paul Ehrlich Society for Chemotherapy e. V. In: Chemotherapy Journal. 11, 2002, pp. 47-58.
  4. ^ H. Scholz, KG Naber and the expert group of the Paul Ehrlich Society for Chemotherapy eV, Chemietherapie Journal 8, 1999, pp. 227–229 (PDF) ( Memento from September 20, 2009 in the Internet Archive ).
  5. a b Recommendations of an expert commission of the Paul Ehrlich Society for Chemotherapy e. V., Chemotherapy Journal 15, 2006, pp. 129-145 (PDF) ( Memento from September 20, 2009 in the Internet Archive ).
  6. Cefpodoxime Proxetil - a new cephalosporin for oral use. In: Journal for Infection Therapy. 1992, accessed February 16, 2016 .
  7. ↑ Product information Cefpodoxime Sandoz 100 mg film-coated tablets / 200 mg film-coated tablets / 40 mg / 5 ml powder for oral suspension. As of December 2007.