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Trade names | Invanz |
AHFS/Drugs.com | Monograph |
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Routes of administration |
Intramuscular, intravenous |
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Pharmacokinetic data | |
Bioavailability | 90% (intramuscular) |
Protein binding | Inversely proportional to concentration; 85 to 95% |
Metabolism | Minor hydrolysis of beta-lactam ring, not involved |
Biological half-life | 4 hours |
Excretion | Renal (80%) and fecal (10%) |
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Chemical and physical data | |
Formula | C22H25N3O7S |
Molar mass | 475.516 g/mol |
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(what is this?) |
Ertapenem is a carbapenem antibiotic marketed by Merck as Invanz. It is structurally very similar to meropenem in that it possesses a 1-β-methyl group. Other members of the carbapenem group (imipenem, doripenem, and meropenem) are broadly active antibacterials that are used for infections caused by difficult to treat or multidrug-resistant bacteria (such as ESBL expressing Klebsiella pneumonia). They have very short serum half-lives and must be administered by intravenous infusion every 6 to 8 hours. Ertapenem differs from other carbapenems in having a somewhat less broad spectrum of activity (not against Pseudomonas aeruginosa), and in that its extended serum half-life allows it to be administered once every 24 hours.
Ertapenem has been designed to be effective against Gram-negative and Gram-positive bacteria. It is not active against MRSA, ampicillin-resistant enterococci, Pseudomonas aeruginosa, or Acinetobacter species. Ertapenem also has clinically useful activity against anaerobic bacteria.
Ertapenem has been shown to be active against most isolates of the following micro-organisms in vitro and in clinical infections.
Aerobic and facultative gram-positive microorganisms: Staphylococcus aureus (methicillin-susceptible isolates only), Streptococcus agalactiae, Streptococcus pneumoniae (penicillin-susceptible isolates only), Streptococcus pyogenes,
Note: Methicillin-resistant staphylococci and Enterococcus spp. are resistant to ertapenem.