Drug Guide
Ertapenem Sodium
Classification
Therapeutic: Antibiotic, Carbapenem
Pharmacological: Beta-lactam antibiotic, Carbapenem
FDA Approved Indications
- Treatment of complicated intra-abdominal infections, including post-surgical peritonitis; complicated skin and skin structure infections; community-acquired pneumonia; acute pelvic infections; Diabetic foot infections.
- Note: Use according to susceptibility data and clinical judgment.
Mechanism of Action
Ertapenem inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins, leading to cell death. It has broad-spectrum activity against many gram-positive, gram-negative, and anaerobic bacteria.
Dosage and Administration
Adult: 1 g IV once daily; dosage may be adjusted based on infection site and severity.
Pediatric: Not officially approved for pediatric use; off-label use should be guided by clinical judgment and weight-based dosing.
Geriatric: No specific dosage adjustment needed; monitor renal function as in other populations.
Renal Impairment: Adjusted dosing in patients with creatinine clearance <30 mL/min: 1 g every 48 hours.
Hepatic Impairment: No dosage adjustment required.
Pharmacokinetics
Absorption: Not absorbed orally; administered IV or IM.
Distribution: Widely distributed in body tissues and fluids, including pleural, pericardial, and cerebrospinal fluids (CSF).
Metabolism: Minimal hepatic metabolism; primarily excreted unchanged.
Excretion: Primarily through renal excretion (glomerular filtration and tubular secretion).
Half Life: Approximately 4 hours.
Contraindications
- Hypersensitivity to ertapenem, other carbapenems, or beta-lactam antibiotics.
Precautions
- Use with caution in patients with history of allergies to penicillins or cephalosporins.
- Caution in patients with renal impairment; monitor renal function closely.
Adverse Reactions - Common
- Gastrointestinal disturbances (nausea, vomiting, diarrhea) (Common)
- Headache (Less common)
Adverse Reactions - Serious
- Seizures (Rare, mostly in patients with CNS disorders or renal impairment)
- Allergic reactions (anaphylaxis, Stevens-Johnson syndrome) (Rare)
Drug-Drug Interactions
- Probenecid may decrease renal clearance, increasing ertapenem levels.
- Valproic acid/sevreric acid: may decrease serum levels of valproic acid, increasing risk of seizures.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor for signs of allergic reactions, superinfection, and changes in renal function.
Diagnoses:
- Risk for allergic reaction
- Risk for superinfection
- Impaired renal function
Implementation: Administer as directed, monitor renal function, and observe for adverse reactions.
Evaluation: Assess effectiveness of therapy and discontinue if adverse effects occur.
Patient/Family Teaching
- Report any signs of allergic reactions or severe diarrhea.
- Complete the full course of therapy.
- Maintain adequate hydration.
Special Considerations
Black Box Warnings:
- Serious and sometimes fatal hypersensitivity reactions may occur in individuals allergic to penicillins or other beta-lactams.
Genetic Factors: N/A
Lab Test Interference: May cause false-positive results for urinary glucose with dipstick testing, especially when using p-dihydroxybenzene (false-positive with certain test strips).
Overdose Management
Signs/Symptoms: Nephrotoxicity, neurotoxicity, including seizures, especially in patients with impaired renal function or CNS disorders.
Treatment: Supportive care, maintain hydration, monitor renal function, consider hemodialysis if severe overdose occurs.
Storage and Handling
Storage: Store at room temperature (20°C to 25°C), protected from light and moisture.
Stability: Stable for up to 24 months when stored properly.