Erpen IM/IV Injection

Ertapenem for Injection is a sterile, synthetic, long-acting, parenteral, 1-β methyl-carbapenem that is structurally related to beta-lactam antibiotics, such as penicillins and cephalosporins, with activity against a wide range of Gram-positive and Gram-negative aerobic and anaerobic bacteria.

Ertapenem exhibits a bactericidal mode of action. It works by binding to and inhibiting bacterial penicillin-binding proteins (PBPs). In Escherichia coli, it has a strong affinity toward PBPs 1a, 1b, 2, 3, 4 and 5 with preferential binding to PBPs 2 and 3. Upon binding to PBPs, ertapenem inhibits bacterial cell wall synthesis by interfering with the lengthening and strengthening of the peptidoglycan portion of the cell wall, thereby inhibiting cell wall synthesis.

Adults (>12 years): 1 gm given once a day.

Pediatric (3 months to 12 years): 15 mg/kg twice daily (not to exceed 1 g/day).

Ertapenem may be administered by IV infusion or IM injection. When administered intravenously, it should be infused over a period of 30 minutes.

IM administration of Ertapenem may be used as an alternative to IV administration in the treatment of those infections for which intramuscular therapy is appropriate.

The usual duration of therapy with Ertapenem is 3 to 14 days but varies by the type of infection and causative pathogen(s). When clinically indicated, a switch to an appropriate oral antimicrobial maybe implemented if clinical improvement has been observed.

Prophylaxis of surgical site infection following elective colorectal surgery: To prevent surgical site infections following surgery in adults, the recommended dosage is 1 g IV administered as a single intravenous dose given 1 hour prior to the surgical incision.

Patients with renal insufficiency: Ertapenem may be used for the treatment of infections in adult patients with renal insufficiency. In patients whose creatinine clearance is >30 mL/min no dosage adjustment is necessary. Adult patients with advanced renal insufficiency (creatinine clearance ≤30 mL/min), including those on haemodialysis, should receive 500 mg daily.

There are no data in paediatric patients with renal insufficiency.

Patients on Haemodialysis: If Ertapenem is given at least 6 hours prior to haemodialysis, no supplementary dose is needed. When adult patients on haemodialysis are given Ertapenem within 6 hours prior to haemodialysis, a supplementary 30% dose is recommended following the haemodialysis session. There are no data in patients undergoing peritoneal dialysis or haemofiltration. There are no data in paediatric patients on haemodialysis.

No dosage adjustment is recommended in patients with impaired hepatic function

Preparation for intravenous administration:

• Do not mix or co-infuse Ertapenem with other medications
• Do not use diluents containing Dextrose
• Ertapenem must be reconstituted and then diluted prior to administration
• Reconstitute the contents of a 1 g vial of Ertapenem with 10 ml of one of the following: Water for Injection, 0.9% Sodium Chloride Injection (normal saline) or Bacteriostatic Water for Injection
• Shake well to dissolve and immediately transfer contents of the reconstituted vial to 50 ml normal saline (0.9% Sodium Chloride)
• Complete the infusion within 6 hours of reconstitution

Preparation for intramuscular administration:

• Reconstitute the contents of a 1 gm vial of Ertapenem with 3.2 mL of 1% Lidocaine HCl injection. Shake vial thoroughly to form solution.
• Immediately withdraw the contents of the vial according to the recommended dose and administer by deep intramuscular injection into a large muscle
• The reconstituted IM solution should be used within 1 hour after preparation.

Note: The reconstituted solution for IM injection should not be administered intravenously.

Parenteral drug products should be inspected visually for particulate matter and discolouration prior to use, whenever solution and container permit. Solutions of Ertapenem range from colourless to pale yellow. Variations of colour within this range do not affect the potency of the product.

When Erpen is administered with probenecid, probenecid competes for active tubular secretion and thus inhibits the renal excretion of Erpen. This leads to small but statistically significant increases in the elimination half-life (19%) and in the extent of systemic exposure (25%). No dosage adjustment is necessary when Erpen is given with probenecid. Because of the small effect on half-life, the co-administration with probenecid to extend the half-life of Erpen is not recommended. Other than with probenecid, no specific clinical drug interaction studies have been conducted. Decreased serum levels of valproic acid with co-administration of Erpen have been reported. Careful monitoring of serum levels of valproic acid should be considered if Erpen is to be co-administered with valproic acid.

Ertapenem is contraindicated in patients with known hypersensitivity to any component of this product or to other drugs in the same class or in patients who have demonstrated anaphylactic reactions to beta-lactams. Due to the use of lidocaine HCl as a diluent, intramuscular administration of Ertapenem is contraindicated in patients with a known hypersensitivity to local anaesthetics of the amide type and in patients with severe shock or heart block.

Most adverse experiences reported in these clinical studies were described as mild to moderate in severity. The most common drug-related adverse experiences reported during parenteral therapy with Erpen include Headache, Infused vein complication, phlebitis/ thrombophlebitis, Diarrhoea, nausea and vomiting.

Other uncommon side effects include- Dizziness, somnolence, insomnia, seizure, confusion, Extravasation, hypotension, Dyspnoea, Oral candidiasis, constipation, acid regurgitation, C. difficile-associated diarrhoea, dry mouth, dyspepsia, anorexia, Erythema, pruritus, Abdominal pain, taste perversion, asthenia/fatigue, candidiasis, oedema/swelling, fever, pain, chest pain, Vaginal pruritus.

Ertapenem has been assigned to pregnancy category B by the FDA. There are no adequate and well-controlled studies in pregnant women. Ertapenem should be used during pregnancy only if the potential benefit justifies the potential risk to the mother and foetus. Ertapenem is excreted in human milk. Caution should be exercised when Ertapenem is administered to a nursing woman.

Before initiating therapy with Erpen, careful inquiry should be made concerning previous hypersensitivity reactions to penicillins, cephalosporins, other beta-lactams and other allergens. If an allergic reaction to Erpen occurs, discontinue the drug immediately. Serious anaphylactic reactions require immediate emergency treatment.

As with other antibiotics, prolonged use of Erpen may result in overgrowth of non-susceptible organisms. Repeated evaluation of the patient's condition is essential. If superinfection occurs during therapy, appropriate measures should be taken.

Pseudomembranous colitis has been reported with nearly all antibacterial agents, including Erpen, and may range in severity from mild to life-threatening. Therefore, it is important to consider this diagnosis in patients who present with diarrhoea subsequent to the administration of antibacterial agents. Studies indicate that a toxin produced by Clostridium difficile is a primary cause of "antibiotic-associated colitis".

Pediatric Use: Safety and effectiveness of Erpen in pediatric patients 3 months to 17 years of age are supported by evidence from adequate and well-controlled trials in adults, pharmacokinetic data in pediatric patients, and additional data from comparator-controlled trials in pediatric patients 3 months to 17 years of age.

Geriatric Use: Erpen is known to be substantially excreted by the kidney, and the risk of toxic reactions to Erpen may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function

Patients with Renal Impairment: Dosage adjustment is necessary in patients with creatinine clearance 30 mL/min or less.

Patients with Hepatic Impairment: The pharmacokinetics of Erpen in patients with hepatic impairment have not been established.

No specific information is available on the treatment of overdosage with Erpen. Intravenous administration of Erpen at a 3 g daily dose for 8 days to healthy adult volunteers did not result in significant toxicity. In pediatric clinical studies, a single IV dose of 40 mg/kg up to a maximum of 2 g did not result in toxicity. In the event of an overdose, Erpen should be discontinued and general supportive treatment given until renal elimination takes place. Erpen can be removed by haemodialysis; however, no information is available on the use of haemodialysis to treat overdosage.

Other beta-lactam Antibiotics

For injection: Store at 2-8°C. Keep away from light and out of the reach of children. For auxiliaries pack: Do not store above 30°C. Keep away from light and out of the reach of children.