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 broad‑spectrum carbapenem antibiotic presented as a sterile injectable powder for intravenous administration. It is indicated for the treatment of serious Gram‑negative and Gram‑positive bacterial infections, including complicated intra‑abdominal infections, complicated urinary tract infections, skin and soft‑tissue infections, and nosocomial pneumonia in adult patients.

GNH India supplies Imipenem/Cilastatin Kabi as a licensed, GMP‑certified, GDP‑compliant international pharmaceutical supplier, providing reliable bulk shipments to hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide, and supporting therapeutic programs.

Manufacturer / TM Owner

Fresenius Kabi Deutschland Gmbh

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Indications & Clinical Uses

Imipenem/Cilastatin is a carbapenem antibiotic used to treat severe bacterial infections in various organ systems.

  • Complicated intra‑abdominal infections: eradicates the causative pathogens, leading to resolution of infection and prevention of sepsis.
  • Complicated urinary tract infections: eliminates Gram‑negative uropathogens, improving urinary symptoms and preventing renal complications.
  • Skin and soft‑tissue infections: clears bacterial involvement in cellulitis, abscesses, and wound infections, promoting healing.
  • Nosocomial pneumonia: treats hospital‑acquired lung infections caused by resistant organisms, supporting respiratory recovery.

How It Works

  • Imipenem exerts its antibacterial effect by binding to penicillin‑binding proteins (PBPs) on the bacterial cell wall, inhibiting the final transpeptidation step of peptidoglycan synthesis. This disruption weakens the cell wall, causing osmotic instability and bacterial lysis. Cilastatin is co‑administered to inhibit renal dehydropeptidase‑I, preventing rapid hydrolysis of imipenem and thereby increasing its plasma concentration and therapeutic efficacy.

Side Effects

Imipenem/Cilastatin may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Nausea: mild gastrointestinal upset occurring in many patients.
  • Diarrhea: loose stools that may be self‑limiting.
  • Rash: skin erythema or pruritus.
  • Injection site pain: discomfort at the intravenous site.
  • Elevated liver enzymes: transient increase in hepatic transaminases.

Serious or Rare Side Effects

  • Seizures: risk increased in patients with CNS disorders or renal impairment.
  • Clostridioides difficile colitis: severe diarrhea due to intestinal flora disruption.
  • Anaphylaxis: acute hypersensitivity reaction with respiratory and circulatory compromise.
  • Renal toxicity: acute kidney injury especially with concomitant nephrotoxic drugs.

Precautions & Warnings

When using Imipenem/Cilastatin, clinicians should observe several safety measures to minimize risk.

  • Renal function assessment: evaluate creatinine clearance before initiating therapy and adjust dose in impairment.
  • Seizure risk: avoid in patients with a history of epilepsy or CNS disorders unless benefits outweigh risks.
  • Hypersensitivity monitoring: discontinue immediately if signs of an allergic reaction appear.
  • Concomitant valproic acid: avoid co‑administration as it can reduce valproate levels and precipitate seizures.
  • Nephrotoxic drug caution: monitor closely when used with aminoglycosides or other nephrotoxic agents.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake the vial.

Avoid Interactions

Imipenem/Cilastatin can interact with other medicines, influencing efficacy or safety.

Major Interactions (Avoid)

  • Valproic acid: co‑administration markedly reduces valproate concentrations, increasing seizure risk.
  • Other carbapenems: concurrent use may lead to additive toxicity without added benefit.

Moderate Interactions (Monitor Closely)

  • Diuretics (e.g., furosemide): may enhance nephrotoxic potential; monitor renal function.
  • Anticoagulants (e.g., warfarin): may alter INR; check coagulation parameters regularly.
  • Oral contraceptives: antibiotics may reduce effectiveness; advise alternative contraception.

Frequently Asked Questions

Imipenem/Cilastatin Kabi is a combination carbapenem antibiotic indicated for the treatment of serious bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, skin and soft‑tissue infections, and hospital‑acquired (nosocomial) pneumonia in adult patients.

Imipenem acts by binding to penicillin‑binding proteins on the bacterial cell wall, blocking the final step of peptidoglycan cross‑linking. This inhibition weakens the cell wall, causing osmotic rupture and bacterial death. Cilastatin is added to prevent renal degradation of imipenem, maintaining effective drug levels.

The dosage of Imipenem/Cilastatin Kabi is determined by the prescribing clinician based on the type and severity of infection, patient weight, renal function, and local antimicrobial guidelines. No fixed regimen is provided here; dosing must be individualized by a qualified healthcare professional.

Safety data for Imipenem/Cilastatin in pregnancy and lactation are limited, and the drug is classified as pregnancy category unknown. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and under close medical supervision.

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 necessary import documentation.

Imipenem/Cilastatin shares a broad spectrum of activity with other carbapenems such as meropenem and ertapenem, but it is often chosen for infections where rapid bactericidal action is required. The addition of cilastatin protects imipenem from renal degradation, potentially allowing higher plasma concentrations compared with imipenem alone.

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

Imipenem/Cilastatin is supplied as a sterile powder for injection and is administered intravenously. The reconstituted solution is infused over a specified period, typically 30 minutes, under aseptic conditions by qualified healthcare personnel.

The most serious adverse events include seizures, especially in patients with pre‑existing CNS disorders or renal impairment, severe allergic reactions such as anaphylaxis, Clostridioides difficile‑associated colitis, and acute kidney injury. Prompt recognition and discontinuation are essential if these events occur.

Patients with a known hypersensitivity to imipenem, cilastatin, or any other carbapenem should avoid this medication. It is also contraindicated in individuals with a history of severe allergic reactions to β‑lactam antibiotics and should be used with caution in those with significant renal dysfunction.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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