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

Imipenem/Cilastatin Eberth

Active Ingredient:
Cilastatin Sodium, Imipenem Monohydrate
Origin:
EU

Imipenem/Cilastatin Eberth (Cilastatin Sodium, Imipenem Monohydrate)

Imipenem, the active ingredient in Imipenem/Cilastatin Eberth, is a carbapenem antibiotic presented as an injection for intravenous use. It treats severe bacterial infections, including complicated intra‑abdominal, urinary tract, skin and soft‑tissue, and respiratory infections in hospitalized patients, while cilastatin protects imipenem from renal degradation.

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

Manufacturer / TM Owner

Dr. Friedrich Eberth Arzneimittel Gmbh

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Indications & Clinical Uses

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

  • Complicated intra‑abdominal infection: provides bacterial eradication in the abdominal cavity.
  • Complicated urinary tract infection: clears resistant uropathogens in the urinary system.
  • Skin and soft‑tissue infection: treats deep or extensive bacterial skin involvement.
  • Community‑acquired and hospital‑acquired pneumonia: combats Gram‑negative and Gram‑positive respiratory pathogens.
  • Severe sepsis: offers rapid bactericidal activity in systemic infection.

How It Works

  • Imipenem binds to multiple penicillin‑binding proteins, inhibiting the final stages of bacterial cell‑wall peptidoglycan synthesis, leading to cell lysis. Cilastatin, co‑administered, inhibits renal dehydropeptidase I, preventing enzymatic degradation of imipenem and thereby maintaining effective plasma and urinary concentrations.

Side Effects

Adverse reactions may occur with any antimicrobial therapy and should be monitored.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: may be watery and self‑limiting.
  • Headache: transient and usually resolves.
  • Rash: erythematous skin eruption.
  • Elevated liver enzymes: transient increase in hepatic transaminases.
  • Injection site pain: local discomfort at the infusion site.

Serious or Rare Side Effects

  • Seizures: risk increases with high doses or renal impairment.
  • Anaphylaxis: severe hypersensitivity reaction requiring immediate intervention.
  • Clostridioides difficile colitis: antibiotic‑associated colitis presenting with profuse diarrhea.
  • Renal toxicity: acute kidney injury in susceptible patients.
  • Severe allergic reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Thrombophlebitis: inflammation of the vein at the infusion site.

Precautions & Warnings

Careful assessment and monitoring are required before and during therapy.

  • Renal function monitoring: adjust dosing in patients with impaired renal clearance.
  • Allergy assessment: avoid in individuals with known carbapenem hypersensitivity.
  • Seizure risk: use cautiously in patients with a history of seizures or CNS disorders.
  • Drug interaction review: evaluate concomitant medications that may lower seizure threshold.
  • Pregnancy and lactation: prescribe only when the potential benefit justifies the potential risk.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Imipenem/Cilastatin may interact with several drugs; awareness helps prevent reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Valproic acid: may lower serum valproate levels, increasing seizure risk.
  • Phenobarbital, carbamazepine, phenytoin: may induce hepatic enzymes, reducing imipenem concentrations.
  • Renal dehydropeptidase inhibitors: can increase imipenem toxicity.

Moderate Interactions (Monitor Closely)

  • Aminoglycosides: additive nephrotoxicity; monitor renal parameters.
  • Loop diuretics: may heighten ototoxic risk when combined with other ototoxic agents.
  • Proton pump inhibitors: limited relevance for IV use but may affect gastric pH if oral formulations are used.

Frequently Asked Questions

Imipenem/Cilastatin is indicated for severe bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, skin and soft‑tissue infections, community‑acquired and hospital‑acquired pneumonia, and severe sepsis. It is administered intravenously in hospitalized patients who require broad‑spectrum coverage.

Imipenem inhibits bacterial cell‑wall synthesis by binding to penicillin‑binding proteins, leading to cell lysis. Cilastatin, co‑formulated, blocks renal dehydropeptidase I, preventing the breakdown of imipenem in the kidneys and maintaining therapeutic drug levels.

The specific dose and infusion schedule are determined by the prescribing clinician based on the type and severity of infection, patient weight, renal function, and local antimicrobial guidelines. Dosage adjustments may be required for renal impairment.

Safety data in pregnancy and lactation are limited. The drug should be used only if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision should be made by the treating physician.

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 import documentation.

Imipenem/Cilastatin offers a broad spectrum of activity against many Gram‑negative, Gram‑positive, and anaerobic bacteria and is often chosen for its stability against beta‑lactamases. Compared with meropenem or ertapenem, it may have a slightly higher seizure risk at high doses but provides similar efficacy in severe infections.

The product should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. Once reconstituted, it should be used promptly according to the manufacturer’s instructions.

Imipenem/Cilastatin is given by intravenous infusion. The infusion rate and duration are set by the healthcare professional, typically over 30 minutes to one hour, depending on the clinical situation and patient tolerance.

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. Prompt recognition and management of these reactions are essential.

Patients with a known hypersensitivity to imipenem, cilastatin, or other carbapenems should avoid the drug. Caution is also advised for individuals with a history of seizures, severe renal impairment, or those receiving interacting medications that significantly lower seizure threshold.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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