Product image of Imipenem/Cilastatina Kabi (Cilastatin Sodium, Imipenem Monohydrate) supplied by GNH India

Imipenem/Cilastatina Kabi

Active Ingredient:
Cilastatin Sodium, Imipenem Monohydrate
Origin:
EU

Imipenem/Cilastatina Kabi (Cilastatin Sodium, Imipenem Monohydrate)

Imipenem, the active ingredient in Imipenem/Cilastatin Kabi, is a carbapenem antibiotic presented as an injectable solution for intravenous use. It often treats a broad spectrum of serious bacterial infections in hospitalized adult patients, including intra‑abdominal, urinary, skin, and respiratory infections, and sepsis.

GNH India supplies Imipenem/Cilastatin Kabi as a licensed, GDP‑compliant international pharmaceutical product to hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable logistics support for global distribution. All shipments are accompanied by full regulatory documentation.

Manufacturer / TM Owner

Fresenius Kabi España S.A.U.

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Indications & Clinical Uses

Imipenem/cilastatin is a carbapenem antibiotic used to treat serious bacterial infections across several organ systems.

  • Complicated intra‑abdominal infections: provides rapid bacterial clearance in patients with intra‑abdominal sepsis.
  • Complicated urinary tract infections: eradicates resistant uropathogens causing pyelonephritis and cystitis.
  • Skin and soft tissue infections: treats severe cellulitis, abscesses, and necrotizing infections.
  • Febrile neutropenia: offers broad‑spectrum coverage for neutropenic patients with fever.
  • Pneumonia: effective against hospital‑acquired and ventilator‑associated pneumonia.

How It Works

  • Imipenem binds to penicillin‑binding proteins on bacterial cell walls, inhibiting the final transpeptidation step of peptidoglycan synthesis, which leads to cell lysis. Cilastatin, co‑administered, inhibits renal dehydropeptidase‑I, preventing rapid degradation of imipenem and thereby increasing its plasma concentration and antibacterial activity. This dual action expands the spectrum to include many Gram‑negative, Gram‑positive and anaerobic organisms, including those resistant to other β‑lactams.

Side Effects

Adverse reactions to Imipenem/cilastatin may vary in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: may be watery and self‑limiting.
  • Rash: localized skin erythema.
  • Elevated liver enzymes: transient increase in ALT/AST.
  • Headache: mild discomfort.

Serious or Rare Side Effects

  • Seizures: especially in patients with renal impairment or high doses.
  • Anaphylaxis: acute, potentially life‑threatening hypersensitivity.
  • Severe neutropenia: marked reduction in white blood cells.
  • Clostridioides difficile colitis: antibiotic‑associated severe diarrhea.
  • Stevens‑Johnson syndrome: rare mucocutaneous reaction.

Precautions & Warnings

Before prescribing Imipenem/cilastatin, clinicians should consider several safety precautions.

  • Renal function: adjust dose in patients with impaired kidney function.
  • History of seizures: avoid or monitor closely in individuals with prior seizure disorders.
  • Allergies: contraindicated in patients with known hypersensitivity to β‑lactams.
  • Concomitant valproic acid: monitor for decreased valproate levels and seizure risk.
  • Pregnancy and lactation: use only if benefits outweigh potential risks, as safety data are limited.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Imipenem/cilastatin can interact with other medicines, affecting efficacy or safety.

Major Interactions (Avoid)

  • Valproic acid: reduces valproate concentrations, increasing seizure risk.
  • Carbapenem antibiotics with other β‑lactams: may cause antagonistic effects.
  • Probenecid: may increase imipenem plasma levels, raising toxicity risk.

Moderate Interactions (Monitor Closely)

  • Diuretics (e.g., furosemide): may enhance nephrotoxic potential.
  • Anticoagulants (warfarin): monitor INR as imipenem may alter coagulation.
  • CNS depressants: may potentiate seizure threshold lowering.

Frequently Asked Questions

Imipenem/Cilastatin Kabi is a carbapenem antibiotic indicated for the treatment of serious bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, severe skin and soft‑tissue infections, febrile neutropenia, and both hospital‑acquired and ventilator‑associated pneumonia.

Imipenem inhibits penicillin‑binding proteins, blocking the final step of bacterial cell‑wall synthesis, which leads to cell lysis. Cilastatin is co‑administered to inhibit renal dehydropeptidase‑I, preventing rapid breakdown of imipenem and maintaining effective plasma concentrations.

The dosage of Imipenem/Cilastatin is individualized by the prescribing clinician based on the type and severity of infection, patient weight, renal function, and local susceptibility patterns. No fixed regimen is provided here; the prescriber determines the appropriate dose and infusion schedule.

Safety data for Imipenem/Cilastatin in pregnancy and lactation are limited. It should be used only when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision should be made by the treating physician.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request trade or institutional credentials before providing pricing, availability, shipping details (including cold‑chain where required) and import documentation.

Imipenem/Cilastatin offers a broad spectrum that includes many Gram‑negative, Gram‑positive and anaerobic organisms, similar to meropenem and doripenem. Its co‑formulation with cilastatin protects against renal degradation, allowing higher plasma levels, while dosing and safety profiles are comparable across the class.

Imipenem/Cilastatin Kabi should be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the vial. Once reconstituted, use the solution promptly according to the product label and discard any remaining solution after the recommended time.

The medication is given as an intravenous infusion. The reconstituted solution is administered over a period specified by the prescriber, typically 30 minutes to 1 hour, and may be given intermittently

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GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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