Meropenem
**Meropenem** is a broad-spectrum, synthetic **carbapenem antibiotic** structurally similar to imipenem. It is highly valued in veterinary medicine as a "big gun" antibiotic for severe, resistant infections. Key characteristics include: * **Broad Spectrum:** Highly effective against many gram-negative bacteria (especially *Enterobacteriaceae*) and anaerobes. It is less active against gram-positive bacteria compared to imipenem. * **Safety Profile:** Unlike imipenem, meropenem does **not** require co-administration with cilastatin and has a significantly lower risk of inducing seizures, making it safer for patients with central nervous system (CNS) disease. * **Administration:** It must be given parenterally (IV or SC). It is advantageous because it can be administered more rapidly and in smaller volumes than imipenem. > **Clinical Pearl:** To practice good antimicrobial stewardship, meropenem should be strictly reserved for documented resistant infections (e.g., multidrug-resistant *E. coli* or *Pseudomonas*) or when first-line options like aminoglycosides are contraindicated due to renal dysfunction.
Mechanism: Meropenem is a bactericidal beta-lactam antibiotic. * It readily penetrates the bacterial cell envelope and binds to specific **penicillin-binding proteins (PBPs)** located inside the bacterial cell wall. * Binding to PBPs โ **inhibition of bacterial cell wall synthesis** โ weakening of the peptidoglycan network โ cell lysis and death. * **Resistance mechanism:** Meropenem is highly resistant to degradation by most beta-lactamases, including penicillinases and cephalosporinases. Furthermore, it is stable against renal **dehydropeptidase-I**, eliminating the need for a protective enzyme inhibitor like cilastatin.
Dosing by species
- Pharmacokinetic data ยท IM injection ยท IM ยท Rapidly absorbed, bioavailability equal to IV dosing.
- Bacteremia/sepsis ยท 24 mg/kg IV q24h (once daily) or 12 mg/kg SC q8h ยท IV/SC ยท q24h or q8h
- UTI ยท 12 mg/kg SC q12h ยท SC ยท q12h
- CNS infections ยท 40 mg/kg IV or SC q8h ยท IV/SC ยท q8h ยท Extrapolated from children; maximum dose per administration is 2 grams.
- Systemic infections ยท 12 mg/kg q8h SC or 24 mg/kg IV q24h (once daily) ยท SC/IV ยท q8h or q24h
- Urinary tract infections ยท 12 mg/kg q12h SC ยท SC ยท q12h
- Susceptible infections ยท 125 mg (total dose) q8h IV or SC ยท IV/SC ยท q8h ยท If serum creatinine greater than 4, may be given q12h.
- Susceptible infections ยท 8 mg/kg IV or SC q8h ยท IV/SC ยท q8h
- Bacteremia/sepsis ยท 24 mg/kg IV q24h (once daily) or 12 mg/kg SC q8h ยท IV/SC ยท q24h or q8h
- UTI ยท 12 mg/kg SC q12h ยท SC ยท q12h
- CNS infections ยท 40 mg/kg IV or SC q8h ยท IV/SC ยท q8h ยท Extrapolated from children; maximum dose per administration is 2 grams.
Routes of administration
Contraindications
- Hypersensitivity to meropenem or other carbapenems
- History of anaphylaxis after receiving any beta-lactam antibiotic
Adverse effects
- Slight hair loss over SC injection sites
- Nausea (reported in humans)
- Vomiting (reported in humans)
- Diarrhea (reported in humans)
Drug interactions
- Aminoglycosides ยท In vitro evidence of synergy against Pseudomonas aeruginosa
- Probenecid ยท May increase serum concentrations and elimination half-life of meropenem
Monitoring
- Clinical efficacy (resolution of infection signs)
- Injection site monitoring (for SC administration)
Overdose
Overdoses of meropenem are unlikely to cause significant toxicity in patients with normal renal function. * In human trials, massive doses (2 grams every 8 hours) failed to demonstrate any significant adverse effects. * **Management:** Should an overdose occur, the drug can be discontinued or the next dose delayed by a few hours. If necessary (e.g., in severe renal failure), meropenem can be removed via hemodialysis.
VetSheet drug reference is intended for licensed veterinary professionals as a clinical decision-support aid, not a substitute for professional judgement or the manufacturerโs current label.