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

Imipenem/Cilastatin Kabi

Active Ingredient:
Cilastatin Sodium, Imipenem Monohydrate
Origin:
EU

Imipenem/Cilastatin 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 treats severe bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, skin and soft tissue infections, nosocomial pneumonia, and septicemia in hospitalized patients.

GNH India supplies Imipenem/Cilastatin Kabi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Fresenius Kabi Hellas Single Member S.A.

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Indications & Clinical Uses

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

  • Complicated intra‑abdominal infections: provides bactericidal activity against mixed aerobic and anaerobic pathogens.
  • Complicated urinary tract infections: eradicates resistant Gram‑negative organisms causing pyelonephritis and cystitis.
  • Skin and soft tissue infections: treats severe cellulitis and wound infections caused by susceptible bacteria.
  • Nosocomial pneumonia: effective against hospital‑acquired lower respiratory tract infections, including ventilator‑associated pneumonia.
  • Septicemia: used for systemic infections caused by susceptible strains when rapid bacterial clearance is required.

How It Works

  • Imipenem binds to penicillin‑binding proteins (PBPs) on bacterial cell walls, inhibiting the final transpeptidation step of peptidoglycan synthesis, which leads to cell lysis and death. Cilastatin is co‑administered to inhibit renal dehydropeptidase‑I, preventing rapid degradation of imipenem and thereby increasing its plasma concentration and antibacterial efficacy.

Side Effects

Adverse reactions may range from mild to severe and should be monitored during therapy.

Common Side Effects

  • Nausea: mild gastrointestinal upset occurring in many patients.
  • Diarrhea: may be watery and self‑limiting.
  • Rash: skin erythema or pruritus.
  • Elevated liver enzymes: transient increase in transaminases.
  • Injection site reactions: pain, erythema, or swelling at the infusion site.
  • Headache: occasional mild headache.

Serious or Rare Side Effects

  • Seizures: risk increases with high doses or renal impairment.
  • Clostridioides difficile‑associated diarrhea: may lead to colitis.
  • Anaphylaxis: severe hypersensitivity reaction requiring immediate medical attention.
  • Severe neutropenia: marked reduction in neutrophil count.
  • Renal toxicity: worsening kidney function, especially with concomitant nephrotoxins.
  • Hepatic failure: rare but potentially life‑threatening liver injury.

Precautions & Warnings

Careful assessment and monitoring are required before and during treatment.

  • Renal function monitoring: adjust dose in patients with impaired renal clearance.
  • Seizure risk: avoid in patients with a history of seizures or central nervous system disorders.
  • Allergy assessment: confirm no known hypersensitivity to β‑lactam antibiotics.
  • Concurrent nephrotoxic drugs: use with caution when combined with other renal‑toxic agents.
  • 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 may interact with several medicines; some require avoidance while others need close monitoring.

Major Interactions (Avoid)

  • Valproic acid: may reduce serum levels, increasing seizure risk.
  • Probenecid: can raise imipenem concentrations, leading to toxicity.
  • CNS stimulants (e.g., phenobarbital): may lower seizure threshold.
  • Cisplatin: additive nephrotoxicity.

Moderate Interactions (Monitor Closely)

  • Loop diuretics: may increase risk of nephrotoxicity.
  • Aminoglycosides: monitor renal function and drug levels.
  • Warfarin: may alter INR; coagulation parameters should be checked regularly.

Frequently Asked Questions

Imipenem/Cilastatin Kabi is indicated for severe bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, skin and soft tissue infections, hospital‑acquired (nosocomial) pneumonia, and septicemia caused by susceptible organisms.

Imipenem inhibits penicillin‑binding proteins, disrupting the final step of bacterial cell‑wall synthesis, which leads to cell lysis. Cilastatin blocks renal dehydropeptidase‑I, preventing rapid breakdown of imipenem and maintaining effective drug concentrations in the bloodstream.

The prescribed dose is determined by the treating physician based on infection severity, the patient’s renal function, and local susceptibility patterns. Dosing regimens are individualized and should follow the prescriber’s instructions and institutional guidelines.

Safety data in pregnancy and lactation are limited, and the product is classified as pregnancy category unknown. It should be used only if the potential benefit justifies any possible risk to the fetus or infant, and the decision must be made by the prescriber.

Submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies, and procurement teams worldwide. After verification of trade or institutional credentials, the sales team will provide pricing, availability, shipping details (including cold‑chain if needed), and import documentation.

Both imipenem/cilastatin and meropenem belong to the carbapenem class and share a broad spectrum against Gram‑negative and Gram‑positive bacteria. Imipenem is often combined with cilastatin to prevent renal degradation, whereas meropenem does not require this inhibitor. Choice depends on local resistance patterns, patient renal function, and specific bacterial susceptibility.

The product should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Once reconstituted, it should be used promptly according to the manufacturer’s instructions and any remaining solution discarded if not used within the recommended time frame.

Imipenem/Cilastatin is supplied as an injectable solution for intravenous infusion. The powder is reconstituted with a compatible diluent, then administered over a prescribed period, typically 30 minutes to 1 hour, under aseptic conditions by qualified healthcare personnel.

The most serious adverse events include seizures, especially in patients with renal impairment or high doses; Clostridioides difficile‑associated colitis; severe allergic reactions such as anaphylaxis; and rare cases of hepatic or renal failure. Prompt medical evaluation is required if any of these occur.

Patients with a known hypersensitivity to imipenem, cilastatin, or any β‑lactam antibiotics should avoid this product. Caution is also advised for individuals with severe renal impairment who cannot be dose‑adjusted, and for those with a history of seizures unless benefits outweigh risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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