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 treats serious 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, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Fresenius Kabi Romania Srl

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Indications & Clinical Uses

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

  • Complicated intra‑abdominal infections: achieves bacterial eradication in the peritoneal cavity and reduces infection‑related mortality.
  • Complicated urinary tract infections: provides rapid bacterial clearance and improves clinical cure rates.
  • Nosocomial pneumonia: delivers broad‑spectrum coverage against resistant Gram‑negative and Gram‑positive pathogens.

How It Works

  • Imipenem binds to penicillin‑binding proteins, inhibiting bacterial cell‑wall synthesis and 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 occur with any antimicrobial therapy and should be monitored.

Common Side Effects

  • Nausea: mild gastrointestinal upset.
  • Diarrhea: may be watery and self‑limiting.
  • Headache: transient and usually resolves.
  • Infusion site reactions: erythema or phlebitis at the injection site.

Serious or Rare Side Effects

  • Seizures: especially in patients with pre‑existing CNS disorders or renal impairment.
  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Clostridioides difficile‑associated diarrhea: can be life‑threatening.
  • Renal impairment: acute kidney injury in susceptible individuals.

Precautions & Warnings

Careful assessment and monitoring are required before and during therapy.

  • Renal function: adjust dose in patients with impaired renal function.
  • Seizure risk: monitor patients with a history of seizures or CNS disorders.
  • Allergy: avoid in individuals with known hypersensitivity to β‑lactam antibiotics.
  • Pregnancy: use only if the potential benefit justifies the potential risk to the fetus.
  • Drug interactions: review concomitant medications that may lower the seizure threshold.
  • Store at 2‑8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Imipenem/Cilastatin can interact with several medicines; some require avoidance while others need close monitoring.

Major Interactions (Avoid)

  • Valproic acid: may reduce plasma valproate levels, increasing seizure risk.
  • Ganciclovir: carbapenems can diminish antiviral efficacy.
  • CNS stimulants: additive risk of seizures.

Moderate Interactions (Monitor Closely)

  • Diuretics: may heighten nephrotoxicity.
  • Probenecid: can increase imipenem plasma concentrations.
  • Other β‑lactam antibiotics: potential for additive toxicity.

Frequently Asked Questions

Imipenem/Cilastatin Kabi is indicated for the treatment of serious bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, skin and soft‑tissue infections, nosocomial pneumonia, and septicemia in hospitalized patients.

Imipenem inhibits bacterial cell‑wall synthesis by binding to penicillin‑binding proteins, leading to cell lysis. Cilastatin, included in the formulation, blocks renal dehydropeptidase I, preventing enzymatic breakdown of imipenem and thereby maintaining effective plasma levels.

The appropriate dose is individualized 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.

Pregnancy safety data are limited; the product is classified as unknown. It should be used only if the expected benefit to the mother outweighs any potential risk to the fetus. Caution is also advised when breastfeeding, as drug excretion in milk is possible.

Enquiries can be submitted via the product page on gnhindia.com, specifying the required quantity. GNH India supplies 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/Cilastatin offers broad‑spectrum activity against many Gram‑negative, Gram‑positive, and anaerobic bacteria, similar to other carbapenems like meropenem. The addition of cilastatin protects imipenem from renal degradation, potentially allowing higher plasma concentrations compared with imipenem alone.

The injectable solution should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Before use, inspect the vial for particulate matter and ensure the solution is at room temperature if required for administration.

Imipenem/Cilastatin is given by intravenous infusion, typically over 30 minutes. The exact infusion rate and schedule are determined by the prescribing clinician based on infection severity and patient-specific factors.

The most serious adverse events include seizures, especially in patients with renal impairment or CNS disorders, severe allergic reactions such as anaphylaxis, and Clostridioides difficile‑associated colitis, which can be life‑threatening.

Patients with a known hypersensitivity to imipenem, cilastatin, or any β‑lactam antibiotics should avoid this product. Caution is also advised for individuals with a history of seizures, severe renal impairment, or those receiving interacting medications listed under major interactions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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