Product image of Imipenem E Cilastatina Sun Pharma Italia Srl (Cilastatin, Imipenem) supplied by GNH India

Imipenem E Cilastatina Sun Pharma Italia Srl

Active Ingredient:
Cilastatin, Imipenem
Origin:
EU

Imipenem E Cilastatina Sun Pharma Italia Srl (Cilastatin, Imipenem)

Imipenem and Cilastatin, the active ingredient in Imipenem E Cilastatina Sun Pharma Italia Srl, is a carbapenem antibiotic presented as an injectable solution for intravenous use. It treats complicated intra‑abdominal infections, complicated urinary tract infections, skin and soft tissue infections, and febrile neutropenia in hospitalized patients.

GNH India supplies Imipenem E Cilastatina Sun Pharma Italia Srl as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies, clinics and research institutions worldwide.

Manufacturer / TM Owner

Sun Pharmaceutical Industries Europe B.V.

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Indications & Clinical Uses

Imipenem and Cilastatin is a broad‑spectrum carbapenem antibiotic used for serious bacterial infections.

  • Complicated intra‑abdominal infections: provides bacterial eradication and clinical cure in patients with intra‑abdominal sepsis.
  • Complicated urinary tract infections: eliminates resistant uropathogens and resolves infection signs.
  • Skin and soft tissue infections: treats severe cellulitis and wound infections caused by susceptible organisms.
  • Febrile neutropenia: offers empiric coverage against Gram‑negative and Gram‑positive pathogens in neutropenic patients.

How It Works

  • Imipenem binds to multiple penicillin‑binding proteins, inhibiting the final stages of peptidoglycan cross‑linking and causing bacterial cell wall rupture. Cilastatin is co‑administered to inhibit renal dehydropeptidase‑I, preventing rapid hydrolysis of imipenem and thereby increasing its plasma concentration and urinary excretion. The combined effect results in potent, time‑dependent bactericidal activity against a wide range of Gram‑negative, Gram‑positive and anaerobic organisms.

Side Effects

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

Common Side Effects

  • Nausea: mild gastrointestinal upset.
  • Diarrhea: watery or loose stools.
  • Injection site pain: local discomfort at the infusion site.
  • Rash: mild skin erythema.

Serious or Rare Side Effects

  • Seizures: risk increases with high doses or renal impairment.
  • Anaphylaxis: severe allergic reaction requiring immediate treatment.
  • Clostridioides difficile colitis: antibiotic‑associated diarrhea.
  • Neutropenia: marked reduction in white blood cells.

Precautions & Warnings

When using Imipenem and Cilastatin, clinicians should observe several precautionary measures to minimise risk.

  • Renal function: adjust dose in patients with impaired kidney function.
  • CNS effects: monitor for seizures, especially in patients with a history of epilepsy or high‑dose therapy.
  • Hypersensitivity: avoid in individuals with known β‑lactam allergy.
  • Electrolytes: correct hypokalemia and hypomagnesemia before infusion to reduce neurotoxicity.
  • Concomitant antibiotics: use with caution when combined with other nephrotoxic or neurotoxic agents.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Imipenem and Cilastatin can interact with other medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • Valproic acid: concomitant use may reduce valproate levels and precipitate seizures.
  • Monoamine oxidase inhibitors: carbapenems may increase risk of hypertensive crisis.

Moderate Interactions (Monitor Closely)

  • Diuretics (e.g., furosemide): may increase risk of electrolyte disturbances and neurotoxicity.
  • CNS depressants (e.g., phenobarbital): may lower seizure threshold.
  • Other nephrotoxic drugs (e.g., aminoglycosides): heightened risk of renal impairment.
  • Oral contraceptives: carbapenems may reduce hormonal efficacy, consider backup contraception.

Frequently Asked Questions

Imipenem E Cilastatina is indicated for the treatment of serious bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, skin and soft tissue infections, and febrile neutropenia in hospitalized patients. It is reserved for infections caused by organisms susceptible to carbapenems.

Imipenem inhibits bacterial cell wall synthesis by binding to penicillin‑binding proteins, which blocks the cross‑linking of peptidoglycan strands and leads to cell lysis. Cilastatin is added to protect imipenem from rapid degradation by renal dehydropeptidase‑I, thereby maintaining effective drug concentrations.

The dosage of Imipenem E Cilastatina is determined by the prescribing clinician based on the type and severity of infection, renal function, and patient weight. Only a qualified healthcare professional should set the dosing regimen.

The safety of Imipenem E Cilastatina in pregnancy and lactation has not been fully established. It should be used only if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by the treating physician.

To place an order, submit an enquiry on the product page at gnhindia.com with 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 combined with cilastatin offers a broad spectrum of activity similar to other carbapenems such as meropenem, but the addition of cilastatin specifically protects imipenem from renal degradation, allowing higher and more sustained plasma levels. Choice of agent depends on local susceptibility patterns, patient renal function and safety profile.

The product should be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the vial. Once reconstituted, use according to the manufacturer’s stability guidelines and discard any remaining solution after the recommended time.

Imipenem E Cilastatina is supplied as an injectable solution for intravenous infusion. It is administered by a healthcare professional, typically over 30 minutes to 1 hour, depending on the prescribed dose and patient condition.

Serious adverse reactions include seizures, especially in patients with renal impairment or high doses, anaphylactic shock, Clostridioides difficile‑associated colitis, and neutropenia. Prompt recognition and appropriate medical management are essential if these events occur.

Patients with a known hypersensitivity to imipenem, cilastatin, or any β‑lactam antibiotics should avoid this medication. Caution is also advised for individuals with a history of seizures, severe renal impairment, or those receiving interacting drugs such as valproic acid.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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