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 injection solution for intravenous use. It treats serious bacterial infections such as complicated intra‑abdominal infections, urinary tract infections, lower respiratory tract infections, skin and soft‑tissue infections, 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 Deutschland Gmbh

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Indications & Clinical Uses

Imipenem/Cilastatin is a carbapenem antibiotic used for severe bacterial infections affecting various organ systems.

  • Complicated intra‑abdominal infections: provides broad‑spectrum coverage against aerobic and anaerobic pathogens, facilitating clinical cure.
  • Complicated urinary tract infections: eradicates resistant Gram‑negative and Gram‑positive organisms, improving urinary sterility.
  • Hospital‑acquired or community‑acquired lower respiratory tract infections: treats pneumonia caused by susceptible bacteria, supporting respiratory recovery.
  • Skin and soft‑tissue infections: combats mixed flora in severe cellulitis or wound infections, aiding healing.
  • Febrile neutropenia: offers empiric therapy for neutropenic patients at risk of bacterial sepsis, reducing fever duration.

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, co‑formulated in the same preparation, inhibits renal dehydropeptidase I, preventing enzymatic degradation of imipenem and thereby increasing its urinary concentration and systemic exposure.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: often self‑limiting, may be caused by altered gut flora.
  • Vomiting: occasional emesis following infusion.
  • Injection site pain: discomfort at the IV site.
  • Headache: transient cranial discomfort.
  • Elevated liver enzymes: mild, reversible changes in hepatic function tests.

Serious or Rare Side Effects

  • Seizures: risk increases with high doses or renal impairment.
  • Severe allergic reactions: anaphylaxis or Stevens‑Johnson syndrome.
  • Clostridioides difficile‑associated diarrhea: may lead to colitis.
  • Renal dysfunction: acute kidney injury in susceptible patients.
  • Thrombophlebitis: inflammation of veins at infusion site.

Precautions & Warnings

Before initiating Imipenem/Cilastatin therapy, clinicians should consider several safety measures.

  • Renal function assessment: adjust dose in patients with impaired clearance.
  • History of seizures: avoid or monitor closely in individuals with CNS disorders.
  • Allergy evaluation: confirm no known hypersensitivity to β‑lactams or carbapenems.
  • Concomitant valproic acid use: anticipate reduced antiepileptic levels.
  • Pregnancy and lactation: use only if benefits outweigh potential risks (Category B1).
  • 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 antiepileptic concentrations, risking seizure breakthrough.
  • Carbapenem antibiotics with other β‑lactams: may increase risk of additive toxicity.
  • Probenecid: may elevate plasma levels, enhancing toxicity.

Moderate Interactions (Monitor Closely)

  • Diuretics (e.g., furosemide): monitor renal function and electrolytes.
  • Aminoglycosides: watch for nephrotoxicity when combined.
  • Oral contraceptives: possible reduction in effectiveness, advise backup contraception.

Frequently Asked Questions

Imipenem/Cilastatin Kabi is indicated for severe bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, community‑acquired or hospital‑acquired lower respiratory tract infections, skin and soft‑tissue infections, and febrile neutropenia in patients with compromised immune systems.

Imipenem inhibits bacterial cell‑wall synthesis by binding to penicillin‑binding proteins, leading to cell lysis. Cilastatin is not an antibiotic; it blocks renal dehydropeptidase I, an enzyme that would otherwise degrade imipenem, thereby preserving its activity and increasing urinary concentrations.

The prescribing clinician determines the appropriate dose of Imipenem/Cilastatin Kabi based on the infection type, severity, patient weight, renal function, and local antimicrobial susceptibility patterns. No fixed regimen is provided here.

Imipenem/Cilastatin is classified as pregnancy category B1, indicating that animal studies have not shown risk and there are no adequate human studies. It should be used only if the potential benefit justifies the potential risk to the fetus. Limited data are available for breastfeeding; caution is advised.

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, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if required) and necessary import documentation.

Both imipenem/cilastatin and meropenem belong to the carbapenem class and offer broad‑spectrum activity against Gram‑negative, Gram‑positive and anaerobic bacteria. Imipenem is co‑formulated with cilastatin to prevent renal degradation, whereas meropenem does not require this inhibitor. Choice often depends on local resistance patterns, renal function considerations, and clinician preference.

Imipenem/Cilastatin Kabi should be stored refrigerated at 2‑8 °C. The vial must be kept in its original packaging, protected from light, and should not be frozen or shaken. Once reconstituted, the solution should be used promptly according to the manufacturer’s stability guidelines.

The medication is supplied as an injectable solution for intravenous infusion. It is administered by a healthcare professional through a peripheral or central IV line, typically over a short infusion period as directed by the prescriber. Compatibility with other IV fluids should be confirmed before mixing.

Serious adverse events include seizures, especially in patients with renal impairment or high doses; severe hypersensitivity reactions such as anaphylaxis or Stevens‑Johnson syndrome; Clostridioides difficile‑associated colitis; and acute renal dysfunction. Prompt recognition and medical intervention are essential if these occur.

Patients with a known hypersensitivity to imipenem, cilastatin, or any other carbapenem or β‑lactam antibiotic should avoid this drug. Caution is also advised for individuals with a history of seizures, severe renal impairment, or those receiving valproic acid without appropriate monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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