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

Imipenem/Cilastatine Kabi

Active Ingredient:
Cilastatin Sodium, Imipenem Monohydrate
Origin:
EU

Imipenem/Cilastatine Kabi (Cilastatin Sodium, Imipenem Monohydrate)

Imipenem/cilastatin, 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 febrile neutropenia 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 France S.A.S.

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Indications & Clinical Uses

  • Imipenem/cilastatin is a broad‑spectrum carbapenem antibiotic used for serious bacterial infections.
  • Complicated intra‑abdominal infections: provides bactericidal activity against mixed aerobic and anaerobic pathogens.
  • Complicated urinary tract infections: eradicates Gram‑negative and Gram‑positive organisms resistant to other agents.
  • Skin and soft‑tissue infections: treats severe cellulitis and wound infections caused by susceptible bacteria.
  • Nosocomial pneumonia: effective against hospital‑acquired respiratory pathogens.
  • Febrile neutropenia: used empirically to cover likely bacterial causes in neutropenic patients.

How It Works

  • Imipenem binds to penicillin‑binding proteins, inhibiting the final stages of bacterial cell‑wall peptidoglycan synthesis, which leads to cell lysis. Cilastatin, a renal dehydropeptidase I inhibitor, prevents enzymatic degradation of imipenem in the kidneys, thereby maintaining therapeutic plasma concentrations and extending antibacterial activity.

Side Effects

Adverse reactions may occur with any antimicrobial therapy.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: may be self‑limiting or indicate altered gut flora.
  • Rash: erythematous skin eruption, often transient.
  • Injection site reactions: pain, erythema, or swelling at the infusion site.

Serious or Rare Side Effects

  • Seizures: especially in patients with pre‑existing CNS disorders or high doses.
  • Clostridioides difficile‑associated diarrhea: severe colitis requiring medical attention.
  • Anaphylaxis: rapid onset of respiratory distress, hypotension, and urticaria.
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis: extensive skin detachment and mucosal involvement.

Precautions & Warnings

Careful assessment and monitoring are required before and during therapy.

  • Renal function: adjust dosing in patients with impaired renal clearance.
  • Seizure risk: monitor patients with a history of central nervous system disorders.
  • Allergy: avoid in individuals with known hypersensitivity to carbapenems or β‑lactam antibiotics.
  • Pregnancy: use only when 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 may interact with several co‑administered drugs.

Major Interactions (Avoid)

  • Valproic acid: may reduce plasma concentrations of valproate, risking loss of seizure control.
  • Phenobarbital, phenytoin, carbamazepine: may increase the risk of seizures when combined.
  • Renal dehydropeptidase inhibitors: can raise imipenem levels, increasing toxicity.

Moderate Interactions (Monitor Closely)

  • Aminoglycosides: additive nephrotoxicity; monitor renal function.
  • Loop diuretics: may enhance ototoxic risk when used with aminoglycosides.
  • Proton pump inhibitors: minimal impact but should be reviewed for overall gastric pH effects.

Frequently Asked Questions

Imipenem/Cilastatin Kabi is indicated for serious bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, skin and soft‑tissue infections, nosocomial (hospital‑acquired) pneumonia, and febrile neutropenia in patients with compromised immune systems.

The drug combines imipenem, which binds to penicillin‑binding proteins and blocks bacterial cell‑wall synthesis, with cilastatin, which inhibits renal dehydropeptidase I. This inhibition prevents rapid degradation of imipenem in the kidneys, maintaining effective drug levels to kill susceptible bacteria.

The specific dose and infusion rate are determined by the prescribing clinician based on the type and severity of infection, patient weight, renal function, and local antimicrobial guidelines. Healthcare professionals should follow the product label and institutional protocols.

Safety data in pregnancy are limited, and the product is classified as pregnancy category unknown. It should be used only if the potential benefit to the mother outweighs any possible risk to the fetus. Caution is also advised during breastfeeding, and a risk‑benefit assessment should be performed.

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 logistics if needed), and necessary import documentation.

Imipenem/cilastatin offers a broad spectrum of activity, including many Gram‑negative, Gram‑positive, and anaerobic organisms, and is often used when resistance to other β‑lactams is suspected. Compared with meropenem or ertapenem, imipenem has a slightly broader anaerobic coverage but may have a higher seizure risk at elevated doses.

The injectable solution should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Before administration, the vial should be inspected for particulate matter and discoloration, and the solution should be used within the time frame recommended by the manufacturer after reconstitution.

Imipenem/Cilastatin Kabi is given by intravenous infusion. The infusion rate and duration are set by the prescribing clinician, typically over 30 minutes to one hour, depending on the dose and patient tolerance. Infusion should be performed using aseptic technique and appropriate IV equipment.

Serious adverse events include seizures, especially in patients with pre‑existing CNS disorders or high plasma concentrations, severe allergic reactions such as anaphylaxis, and Clostridioides difficile‑associated colitis. Prompt recognition and medical intervention are essential if any of these events occur.

Patients with a known hypersensitivity to imipenem, cilastatin, or any other carbapenem or β‑lactam antibiotics should avoid this medication. Caution is also advised for individuals with severe renal impairment, a history of seizures, or those receiving interacting drugs that lower the seizure threshold.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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