Piperacillin-tazobactam

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Piperacillin
Systematic (IUPAC) name
(2S,5R,6R)-6-{[(2R)-2-[(4-ethyl-2,3-dioxo-piperazine-
1-carbonyl)amino]-2-phenyl-acetyl]amino}-3,3-dimethyl-
7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
Identifiers
CAS number 66258-76-2
ATC code J01CA12
PubChem 43672
DrugBank APRD00325
Chemical data
Formula C23H26N5O7S 
Mol. mass 516.548 g/mol
Pharmacokinetic data
Bioavailability not absorbed orally
Metabolism largely not metabolised
Half life 36–72 minutes
Excretion 20% in bile, 80% unchanged in urine
Therapeutic considerations
Pregnancy cat.

B

Legal status

POM(UK)

Routes IV, IM

Piperacillin is an extended spectrum beta-lactam antibiotic of the ureidopenicillin class. It is normally used together with a beta-lactamase inhibitor such as tazobactam, which is commercially available as Tazocin, Zobactin or Zosyn. The combination has activity against many Gram-positive and Gram-negative pathogens and anaerobes, including Pseudomonas aeruginosa.

Piperacillin is not absorbed orally, and must therefore be given by intravenous or intramuscular injection; piperacillin/tazobactam is administered intravenously every 6 or 8 hours; the drug may also be given by continuous infusion, but this has not been shown to be superior.[1] Its main uses are in intensive care medicine (pneumonia, peritonitis), some diabetes-related foot infections and empirical therapy in febrile neutropenia (e.g. after chemotherapy).

Trade names and preparations

Piperacillin alone:

  • Pipracil (U.S. only)

Piperacillin/tazobactam:

  • Tazocin (UK, marketed by Wyeth)
  • Tazocin (Japan, marketed by Toyama)
  • Tazocin (New Zealand, marketed by Wyeth)
  • Zosyn (U.S., marketed by Wyeth)
  • Zobactin (India, marketed by GSK)

References

  1. ^ Lau W, Mercer D, Itani K, et al. (2006). "Randomized, open-label, comparative study of piperacillin-tazobactam administered by continuous infusion versus intermittent infusion for treatment of hospitalized patients with complicated intra-abdominal infection". Antimicrob Agents Chemother 50 (11): 3556–61. doi:10.1128/AAC.00329-06. PMID 16940077. 

External links


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  • This page was last modified on 3 August 2008, at 13:52.

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