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

Imipenem Cilastatine Sun

Active Ingredient:
Cilastatin Sodium, Imipenem Monohydrate
Origin:
EU

Imipenem Cilastatine Sun (Cilastatin Sodium, Imipenem Monohydrate)

Imipenem/cilastatin, the active ingredient in Imipenem Cilastatine Sun, is a carbapenem antibiotic presented as a sterile powder for reconstitution for intravenous use. It treats severe bacterial infections such as intra‑abdominal infections, pneumonia, urinary tract infections, skin and soft‑tissue infections, and septicemia in hospitalized patients.
GNH India supplies Imipenem Cilastatine Sun as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Sun Pharma France

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Indications & Clinical Uses

  • Imipenem/cilastatin is a broad‑spectrum carbapenem used for serious bacterial infections across several organ systems.
  • Complicated intra‑abdominal infections: eradicates mixed aerobic and anaerobic pathogens and reduces morbidity.
  • Complicated urinary tract infections: provides rapid bacterial clearance in resistant Gram‑negative infections.
  • Skin and soft‑tissue infections: treats severe cellulitis and necrotizing infections caused by susceptible organisms.
  • Community‑acquired and hospital‑acquired bacterial pneumonia: offers coverage against resistant Streptococcus pneumoniae and Gram‑negative pathogens.
  • Septicemia: delivers bactericidal activity in bloodstream infections caused by susceptible bacteria.

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‑administered as a renal dehydropeptidase I inhibitor, prevents enzymatic degradation of imipenem in the kidneys, thereby maintaining therapeutic plasma concentrations.

Side Effects

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: may be watery and self‑limiting.
  • Vomiting: occasional episodes after infusion.
  • Headache: transient and usually resolves.
  • Rash: mild skin erythema or pruritus.
  • Elevated liver enzymes: transient increase in hepatic transaminases.

Serious or Rare Side Effects

  • Seizures: especially in patients with renal impairment or CNS disorders.
  • Severe allergic reactions: anaphylaxis, angioedema, or Stevens‑Johnson syndrome.
  • Clostridioides difficile colitis: antibiotic‑associated diarrhea that can be severe.
  • Thrombophlebitis: inflammation at the infusion site.
  • Renal toxicity: rare acute kidney injury.
  • Hematologic abnormalities: neutropenia or thrombocytopenia.

Precautions & Warnings

Before initiating therapy, consider the following precautions:

  • Renal function: adjust dosage in patients with impaired renal clearance.
  • Allergy: avoid in individuals with known hypersensitivity to carbapenems or β‑lactams.
  • Seizure risk: monitor closely in patients with a history of seizures or CNS disorders.
  • Drug interactions: review concomitant medications that may lower seizure threshold.
  • Pregnancy: use only if the potential benefit justifies the potential risk to the fetus.
  • Store at below 25°C: keep in the original container, protect from moisture and light.

Avoid Interactions

Imipenem/cilastatin may interact with several drugs; monitoring is advised.

Major Interactions (Avoid)

  • Valproic acid: co‑administration can reduce valproate levels, increasing seizure risk.
  • Cytotoxic chemotherapy agents: may potentiate neurotoxicity when given together.

Moderate Interactions (Monitor Closely)

  • Diuretics (e.g., furosemide): may increase the risk of nephrotoxicity.
  • Probenecid: can raise plasma concentrations of imipenem.
  • Antacids containing magnesium or aluminum: may affect infusion site tolerance, though impact is minimal with IV administration.

Frequently Asked Questions

Imipenem Cilastatine Sun is indicated for severe bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, skin and soft‑tissue infections, community‑acquired or hospital‑acquired bacterial pneumonia, and septicemia. It is reserved for cases where broad‑spectrum coverage is required.

Imipenem inhibits penicillin‑binding proteins, disrupting the final step of bacterial cell‑wall synthesis and causing cell lysis. Cilastatin blocks renal dehydropeptidase I, an enzyme that would otherwise degrade imipenem, thereby preserving its antibacterial activity in the bloodstream.

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

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. Clinicians must evaluate each case individually and discuss risks with the patient.

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 that includes many Gram‑negative, Gram‑positive, and anaerobic organisms, similar to meropenem or ertapenem. Its unique combination with cilastatin protects the drug from renal degradation, allowing higher plasma concentrations, but the choice among carbapenems depends on local resistance patterns and patient-specific factors.

Imipenem Cilastatine Sun should be stored below 25 °C in its original packaging, protected from moisture and light. Once reconstituted, the solution must be used within the time frame specified in the product labeling and kept refrigerated if required by the manufacturer.

The product is supplied as a sterile powder for reconstitution and is administered intravenously. It is typically infused over a specified period, as directed by the prescribing clinician, using aseptic technique and appropriate infusion equipment.

Serious adverse events include seizures, especially in patients with renal impairment or pre‑existing 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, other carbapenems, 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 that significantly lower the seizure threshold.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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