Product image of Imipenem + Cylastatyna Ranbaxy (Cilastatin, Imipenem) supplied by GNH India

Imipenem + Cylastatyna Ranbaxy

Active Ingredient:
Cilastatin, Imipenem
Origin:
EU

Imipenem + Cylastatyna Ranbaxy (Cilastatin, Imipenem)

Imipenem and cilastatin, the active ingredients in Imipenem + Cylastatyna Ranbaxy, are carbapenem antibiotics presented as an intravenous formulation for parenteral use. They treat severe bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, and nosocomial pneumonia in hospitalized patients.

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

Manufacturer / TM Owner

Ranbaxy Poland Sp. Zo.O

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Indications & Clinical Uses

Imipenem/cilastatin is indicated for a range of serious bacterial infections that require broad‑spectrum intravenous therapy.

  • Complicated intra‑abdominal infections: eradicates mixed aerobic and anaerobic pathogens to resolve infection.
  • Complicated urinary tract infections: provides rapid bacterial clearance in resistant Gram‑negative infections.
  • Nosocomial pneumonia: treats hospital‑acquired lung infections caused by multidrug‑resistant organisms.
  • Skin and soft tissue infections: covers a wide spectrum of Gram‑positive and Gram‑negative bacteria.
  • Septicemia: delivers bactericidal activity in bloodstream infections requiring immediate therapy.

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 intravenously inhibits renal dehydropeptidase I, preventing enzymatic degradation of imipenem and thereby maintaining therapeutic plasma concentrations.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Diarrhea: often self‑limiting, may be watery.
  • Injection site pain: localized discomfort during infusion.
  • Elevated liver enzymes: transient increase in transaminases.
  • Rash: non‑specific skin eruption.
  • Headache: mild, transient.

Serious or Rare Side Effects

  • Seizures: especially in patients with renal impairment or high doses.
  • Anaphylaxis: acute, potentially life‑threatening hypersensitivity.
  • Clostridioides difficile colitis: severe diarrhea due to gut flora disruption.
  • Neutropenia: marked reduction in white blood cells.
  • Thrombocytopenia: low platelet count leading to bleeding risk.
  • Renal dysfunction: worsening kidney function in susceptible individuals.

Precautions & Warnings

Use of imipenem/cilastatin requires careful clinical assessment and monitoring.

  • Renal function: adjust dose in patients with impaired kidney function.
  • Seizure risk: avoid high doses in patients with a history of seizures.
  • Hypersensitivity: discontinue immediately if an allergic reaction occurs.
  • Antibiotic stewardship: limit use to confirmed bacterial infections to reduce resistance.
  • Pregnancy and lactation: assess risk‑benefit; limited data available.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Imipenem/cilastatin may interact with other medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • Valproic acid: may reduce valproate levels, risking seizure breakthrough.
  • Probenecid: can increase imipenem concentrations, heightening neurotoxicity.

Moderate Interactions (Monitor Closely)

  • Diuretics (e.g., furosemide): may enhance nephrotoxic potential.
  • Anticoagulants (e.g., warfarin): monitor INR as antibiotic may affect metabolism.
  • Other nephrotoxic agents (e.g., aminoglycosides): assess renal function frequently.
  • CNS depressants: observe for additive central nervous system effects.

Frequently Asked Questions

Imipenem + Cylastatyna is prescribed for serious bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, nosocomial pneumonia, skin and soft tissue infections, and septicemia. It is typically reserved for hospitalized patients where broad‑spectrum intravenous therapy is required.

Imipenem inhibits penicillin‑binding proteins, disrupting bacterial cell‑wall synthesis and causing cell death. Cilastatin is co‑administered to block renal dehydropeptidase I, an enzyme that would otherwise degrade imipenem, thereby preserving its antibacterial activity and extending its plasma half‑life.

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 guidelines. Healthcare professionals should follow the product label and institutional protocols when prescribing.

Safety data in pregnancy and lactation are limited. The drug should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant. Clinicians should discuss the risk‑benefit profile with the patient and consider alternative therapies when appropriate.

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 any cold‑chain requirements), and necessary import documentation.

Imipenem/cilastatin offers a broad spectrum that includes many Gram‑negative, Gram‑positive, and anaerobic organisms, similar to meropenem and ertapenem. Its unique combination with cilastatin protects the drug from renal degradation, allowing higher plasma concentrations. Choice among carbapenems depends on local resistance patterns, pharmacokinetic considerations, and patient-specific factors.

The product should be stored at 2‑8 °C, protected from light, and must not be frozen. Once reconstituted, it should be used within the time frame specified in the package insert and kept refrigerated if not administered immediately.

Imipenem + Cylastatyna is given by intravenous infusion. The infusion rate and duration are set by the prescribing clinician, usually over 30 minutes to 1 hour, depending on the dose and patient tolerance. Administration should follow aseptic technique and institutional infusion protocols.

Serious adverse events include seizures, especially in patients with renal impairment or high doses, anaphylactic reactions, Clostridioides difficile‑associated colitis, and severe neutropenia or thrombocytopenia. Prompt recognition and discontinuation are essential if any of these events occur.

Patients with a known hypersensitivity to imipenem, cilastatin, or any carbapenem 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 without appropriate monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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