Product image of Imipenem E Cilastatina Aurobindo (Cilastatin Sodium, Imipenem Monohydrate) supplied by GNH India

Imipenem E Cilastatina Aurobindo

Active Ingredient:
Cilastatin Sodium, Imipenem Monohydrate
Origin:
EU

Imipenem E Cilastatina Aurobindo (Cilastatin Sodium, Imipenem Monohydrate)

Imipenem, the active ingredient in Imipenem E Cilastatina Aurobindo, is a carbapenem antibiotic presented as an injectable solution for intravenous use. It is combined with cilastatin sodium to broaden antibacterial coverage and is employed in the treatment of serious bacterial infections in hospitalized patients.

GNH India supplies Imipenem E Cilastatina Aurobindo as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide, ensuring quality and regulatory compliance across global markets.

Manufacturer / TM Owner

Eugia Pharma (Malta) Ltd

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Indications & Clinical Uses

Imipenem/cilastatin is a broad‑spectrum carbapenem used for serious bacterial infections affecting various organ systems.

  • Complicated intra‑abdominal infections: provides rapid bacterial eradication and clinical improvement.
  • Complicated urinary tract infections: eliminates resistant uropathogens and resolves infection.
  • Lower respiratory tract infections: treats severe pneumonia caused by Gram‑negative and Gram‑positive organisms.
  • Skin and soft tissue infections: clears deep tissue infections and necrotizing fasciitis.
  • Septicemia: offers bactericidal activity in bloodstream infections.

How It Works

  • Imipenem binds to penicillin‑binding proteins, inhibiting the final stages of bacterial cell‑wall peptidoglycan synthesis, leading to cell lysis. Cilastatin, co‑administered, blocks renal dehydropeptidase I, preventing enzymatic degradation of imipenem and thereby maintaining therapeutic plasma concentrations.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: may be watery and self‑limiting.
  • Headache: transient and usually resolves without intervention.
  • Rash: erythematous skin eruption.
  • Elevated liver enzymes: mild transaminase increase.
  • Injection site pain: discomfort at the infusion site.

Serious or Rare Side Effects

  • Seizures: especially in patients with renal impairment or high doses.
  • Anaphylaxis: acute, potentially life‑threatening hypersensitivity.
  • Clostridioides difficile colitis: severe diarrhea due to gut flora disruption.
  • Renal impairment: acute kidney injury in susceptible individuals.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Thrombocytopenia: marked reduction in platelet count.

Precautions & Warnings

Careful assessment and monitoring are required before and during therapy.

  • Renal function: adjust dose in patients with reduced creatinine clearance.
  • Hepatic function: monitor liver enzymes in patients with pre‑existing liver disease.
  • Hypersensitivity: avoid in individuals with known allergy to carbapenems or β‑lactams.
  • Pregnancy: use only if benefits outweigh potential risks, as data are limited.
  • Concomitant valproic acid: monitor seizure control, as imipenem may lower valproate levels.
  • Storage at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Imipenem/cilastatin can alter or be altered by other medicines.

Major Interactions (Avoid)

  • Valproic acid: reduces serum valproate concentrations, increasing seizure risk.
  • Probenecid: decreases renal clearance of imipenem, raising plasma levels.
  • Renal dehydropeptidase inhibitors: may increase imipenem toxicity.

Moderate Interactions (Monitor Closely)

  • Diuretics (e.g., furosemide): may enhance nephrotoxic potential.
  • Aminoglycosides: combined nephrotoxicity requires renal function monitoring.
  • Oral contraceptives: possible reduction in efficacy, advise additional contraceptive measures.

Frequently Asked Questions

Imipenem E Cilastatina Aurobindo is a combination of imipenem and cilastatin administered intravenously to treat severe bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, lower respiratory tract infections, skin and soft‑tissue infections, and septicemia in hospitalized patients.

Imipenem inhibits bacterial cell‑wall synthesis by binding to penicillin‑binding proteins, causing cell lysis. Cilastatin, co‑formulated, blocks renal dehydropeptidase I, preventing enzymatic degradation of imipenem and preserving its antibacterial activity in the bloodstream.

The dosing regimen for Imipenem E Cilastatina Aurobindo is individualized by the prescribing clinician based on infection severity, site, renal function, and patient weight. Healthcare professionals determine the appropriate dose and infusion schedule.

Safety data in pregnancy and lactation are limited. The drug should be used only if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and it is typically avoided unless no suitable alternatives exist.

To place an order, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed), and import documentation.

Imipenem belongs to the carbapenem class, which also includes meropenem and ertapenem. Compared with meropenem, imipenem has a broader spectrum against Pseudomonas aeruginosa but may have a higher risk of seizures, especially in patients with renal dysfunction. Choice depends on local susceptibility patterns and patient factors.

The product must be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Once reconstituted, it should be used within the time frame specified in the product labeling and kept under the same temperature conditions.

Imipenem E Cilastatina Aurobindo is supplied as a sterile powder for injection. It is reconstituted with the appropriate diluent, then administered intravenously over a prescribed infusion period, usually 30 minutes to 1 hour, under aseptic conditions.

The most serious adverse events include seizures (particularly in patients with renal impairment or high doses), severe hypersensitivity reactions such as anaphylaxis, Clostridioides difficile‑associated colitis, and acute renal injury. Prompt medical attention is required if any of these occur.

Patients with a known hypersensitivity to imipenem, cilastatin, or any carbapenem/β‑lactam antibiotics should avoid this product. Caution is also advised for individuals with a history of seizures, severe renal impairment, or those receiving valproic acid without appropriate monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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