Meropenem



Meropenem
Systematic (IUPAC) name
3-[5-(dimethylcarbamoyl) pyrrolidin-2-yl] sulfanyl-6- (1-hydroxyethyl)-4-methyl-7-oxo- 1-azabicyclo[3.2.0] hept-2-ene-2-carboxylic acid
Identifiers
CAS number 119478-56-7
ATC code J01DH02
PubChem 64778
DrugBank APRD01097
Chemical data
S 
Mol. mass 383.464 g/mol
Pharmacokinetic data
Bioavailability 100%
Protein binding Approximately 2%.
Metabolism  ?
Half life 1 hour
Excretion Renal
Therapeutic considerations
Pregnancy cat.

B

Legal status

℞-only (U.S.)

Routes IV

Meropenem is an ultra-broad spectrum injectable bile, heart valves, lung, and peritoneal fluid.[1]

Mechanism of action

Meropenem is bactericidal except against Listeria monocytogenes where it is bacteriostatic. It inhibits bacterial wall synthesis like other cilastatin.

Indications

The spectrum of action includes many gram-positive and gram-negative bacteria and even some anaerobic bacteria. The overall spectrum is similar to imipenem although meropenem is more active against Enterobacteriaceae and less active against gram-positive bacteria. It is also very resistant to extended-spectrum beta lactamases but may be more susceptible to metallo-beta-lactamases.[1] However, meropenem should not be used to treat MRSA infections.

Administration

Meropenem must be administered intravenously. It is supplied as a white crystalline powder to be dissolved in 5% monobasic potassium phosphate solution.

Common adverse effects

The most common adverse effects are diarrhea (4.8%), nausea and vomiting (3.6%), injection-site inflammation (2.4%), headache (2.3%), rash (1.9%), and thrombophlebitis (0.9%).[2] Many of these adverse effects were observed in the setting of severely ill individuals who were already taking many medications. Meropenem also has a reduced potential for causing seizures in comparison with imipenem.

References

  1. ^ a b (2006) AHFS DRUG INFORMATION® 2006, 2006 ed, American Society of Health-System Pharmacists. 
  2. ^ a b (2006) Mosby's Drug Consult 2006, 16 ed, Mosby, Inc.. 


 
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