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

Imipenem/Cilastatina Aurovitas

Active Ingredient:
Cilastatin Sodium, Imipenem Monohydrate
Origin:
EU

Imipenem/Cilastatina Aurovitas (Cilastatin Sodium, Imipenem Monohydrate)

Imipenem/cilastatin, the active ingredient in Imipenem/Cilastatin Aurovitas, is a carbapenem antibiotic presented as an injectable solution for intravenous use. It provides broad‑spectrum coverage against Gram‑positive, Gram‑negative and anaerobic bacteria and is employed in hospitalized adults and children with serious infections.

GNH India supplies Imipenem/Cilastatin Aurovitas as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and offers reliable global logistics.

Manufacturer / TM Owner

Eugia Pharma (Malta) Ltd

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Indications & Clinical Uses

Imipenem/cilastatin is used for a range of severe bacterial infections affecting various organ systems.

  • Complicated intra‑abdominal infections: provides rapid bacterial eradication to resolve intra‑abdominal sepsis.
  • Complicated urinary tract infections: offers effective clearance of resistant uropathogens in the urinary tract.
  • Skin and soft‑tissue infections: eliminates causative bacteria to promote healing of deep tissue infections.
  • Community‑acquired and hospital‑acquired pneumonia: delivers broad‑spectrum activity to treat pulmonary infections.
  • Meningitis: penetrates the cerebrospinal fluid to treat bacterial meningitis.
  • Febrile neutropenia: offers empiric coverage for neutropenic patients at risk of bloodstream infection.

How It Works

  • Imipenem binds to bacterial penicillin‑binding proteins, inhibiting the transpeptidation step of cell‑wall synthesis and leading to bacterial lysis. Cilastatin, a renal dehydropeptidase I inhibitor, prevents enzymatic degradation of imipenem in the kidneys, thereby maintaining therapeutic concentrations and extending the antibiotic’s activity. This combined action results in a time‑dependent bactericidal effect against a wide spectrum of Gram‑positive, Gram‑negative and anaerobic organisms, including many multidrug‑resistant strains.

Side Effects

Like all antibiotics, Imipenem/cilastatin may cause adverse reactions, ranging from mild to severe.

Common Side Effects

  • Nausea
  • Diarrhea
  • Rash

Serious or Rare Side Effects

  • Seizures, particularly in patients with renal dysfunction or CNS disease
  • Anaphylactic reactions
  • Clostridioides difficile‑associated colitis

Precautions & Warnings

Careful assessment and monitoring are required when using Imipenem/cilastatin.

  • Renal function assessment: evaluate creatinine clearance and adjust dose in renal impairment.
  • Seizure risk: monitor patients with a history of seizures or CNS disorders.
  • Allergy history: avoid in individuals with known hypersensitivity to carbapenems or β‑lactams.
  • Pregnancy and lactation: use only when the potential benefit justifies the potential risk to the fetus or infant.
  • Concomitant medications: review for drugs that may lower seizure threshold or affect renal clearance.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Imipenem/cilastatin can interact with several medicines; some require avoidance while others need close monitoring.

Major Interactions (Avoid)

  • Valproic acid: co‑administration can markedly reduce valproate levels, risking seizure breakthrough.
  • Probenecid: may increase imipenem concentrations and heighten nephrotoxicity.
  • Other carbapenems: concurrent use can lead to additive toxicity without therapeutic benefit.

Moderate Interactions (Monitor Closely)

  • Diuretics: may enhance renal clearance of imipenem, requiring dose consideration.
  • Aminoglycosides: combined nephrotoxic potential warrants renal function monitoring.
  • NSAIDs: can affect renal perfusion and increase risk of renal impairment.

Frequently Asked Questions

Imipenem/Cilastatin Aurovitas is indicated for severe bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, skin and soft‑tissue infections, both community‑acquired and hospital‑acquired pneumonia, bacterial meningitis, and febrile neutropenia in hospitalized patients.

Imipenem inhibits bacterial cell‑wall synthesis by binding to penicillin‑binding proteins, causing bacterial lysis. Cilastatin is a renal dehydropeptidase I inhibitor that prevents the breakdown of imipenem in the kidneys, thereby preserving its antibacterial activity and extending its plasma half‑life.

The dosage is individualized by the prescribing clinician based on the type and severity of infection, the patient’s age, weight, and renal function. Dose adjustments are required for patients with impaired kidney function, and the regimen is typically administered by intravenous infusion under medical supervision.

The pregnancy category for Imipenem/Cilastatin is not definitively established. It should be used during pregnancy or lactation only when the potential therapeutic benefit justifies any potential risk to the fetus or infant, and after careful consideration by the treating physician.

To place an order, submit an enquiry on the product page at gnhindia.com with 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 where required) and necessary import documentation.

Imipenem/Cilastatin offers a broad spectrum similar to meropenem but includes cilastatin to inhibit renal degradation, which can result in higher renal concentrations. Both agents are effective against many resistant Gram‑negative and anaerobic organisms; choice often depends on local susceptibility patterns, dosing convenience, and specific patient factors such as renal function.

The product should be stored at 2‑8 °C (refrigerated). Keep the vial in its original packaging, protect it from light, and do not freeze or shake the solution. Once reconstituted, use according to the manufacturer’s stability guidelines.

Imipenem/Cilastatin is given by intravenous infusion. The vial is reconstituted with the appropriate diluent, then further diluted in compatible IV fluids. Administration is typically over 15‑30 minutes, but infusion time may be adjusted based on patient tolerance and renal function.

Serious adverse events include seizures (especially in patients with renal impairment or CNS disorders), severe hypersensitivity reactions such as anaphylaxis, and Clostridioides difficile‑associated colitis. Prompt recognition and medical intervention are essential if any of these events occur.

Patients with a known hypersensitivity to imipenem, cilastatin, or other carbapenem antibiotics should avoid this drug. Those with uncontrolled severe renal impairment should not receive it without dose adjustment, and it should be used cautiously in patients with a history of seizures or central nervous system disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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