GNH USA

Europe — EMA

Imipenem E Cilastatina Aurobindo

GNH USA supplies Imipenem E Cilastatina Aurobindo (Imipenem/cilastatin), a carbapenem antibiotic for complicated intra‑abdominal, urinary and respiratory

Cilastatin Sodium, Imipenem Monohydrate

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What is Cilastatin Sodium, Imipenem Monohydrate?

Imipenem, the active ingredient in Imipenem E Cilastatina Aurobindo, is a carbapenem antibiotic presented as an injectable solution for intravenous use. It is combined with cilastatin sodium to broaden antibacterial coverage and is employed in the treatment of serious bacterial infections in hospitalized patients.

GNH USA supplies Imipenem E Cilastatina Aurobindo as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide, ensuring quality and regulatory compliance across global markets.

What is Cilastatin Sodium, Imipenem Monohydrate used for?

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

- Complicated intra‑abdominal infections: provides rapid bacterial eradication and clinical improvement. - Complicated urinary tract infections: eliminates resistant uropathogens and resolves infection. - Lower respiratory tract infections: treats severe pneumonia caused by Gram‑negative and Gram‑positive organisms. - Skin and soft tissue infections: clears deep tissue infections and necrotizing fasciitis. - Septicemia: offers bactericidal activity in bloodstream infections.

What are the side effects of Cilastatin Sodium, Imipenem Monohydrate?

Adverse reactions may vary in frequency and severity.

Common Side Effects: - Nausea: mild to moderate gastrointestinal upset. - Diarrhea: may be watery and self‑limiting. - Headache: transient and usually resolves without intervention. - Rash: erythematous skin eruption. - Elevated liver enzymes: mild transaminase increase. - Injection site pain: discomfort at the infusion site.

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. - Renal impairment: acute kidney injury in susceptible individuals. - Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis. - Thrombocytopenia: marked reduction in platelet count.

What precautions apply to Cilastatin Sodium, Imipenem Monohydrate?

Careful assessment and monitoring are required before and during therapy.

- Renal function: adjust dose in patients with reduced creatinine clearance. - Hepatic function: monitor liver enzymes in patients with pre‑existing liver disease. - Hypersensitivity: avoid in individuals with known allergy to carbapenems or β‑lactams. - Pregnancy: use only if benefits outweigh potential risks, as data are limited. - Concomitant valproic acid: monitor seizure control, as imipenem may lower valproate levels. - Storage at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Cilastatin Sodium, Imipenem Monohydrate interact with?

Imipenem/cilastatin can alter or be altered by other medicines.

Major Interactions (Avoid): - Valproic acid: reduces serum valproate concentrations, increasing seizure risk. - Probenecid: decreases renal clearance of imipenem, raising plasma levels. - Renal dehydropeptidase inhibitors: may increase imipenem toxicity.

Moderate Interactions (Monitor Closely): - Diuretics (e.g., furosemide): may enhance nephrotoxic potential. - Aminoglycosides: combined nephrotoxicity requires renal function monitoring. - Oral contraceptives: possible reduction in efficacy, advise additional contraceptive measures.

Frequently asked questions

What is Imipenem E Cilastatina Aurobindo used for?+
Imipenem E Cilastatina Aurobindo is a combination of imipenem and cilastatin administered intravenously to treat severe bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, lower respiratory tract infections, skin and soft‑tissue infections, and septicemia in hospitalized patients.
How does imipenem work?+
Imipenem inhibits bacterial cell‑wall synthesis by binding to penicillin‑binding proteins, causing cell lysis. Cilastatin, co‑formulated, blocks renal dehydropeptidase I, preventing enzymatic degradation of imipenem and preserving its antibacterial activity in the bloodstream.
What is the usual dose of Imipenem E Cilastatina Aurobindo?+
The dosing regimen for Imipenem E Cilastatina Aurobindo is individualized by the prescribing clinician based on infection severity, site, renal function, and patient weight. Healthcare professionals determine the appropriate dose and infusion schedule.
Is Imipenem E Cilastatina Aurobindo safe in pregnancy or breastfeeding?+
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 it is typically avoided unless no suitable alternatives exist.
How do I order Imipenem E Cilastatina Aurobindo from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com specifying the required quantity. GNH USA 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.
How does Imipenem compare with the main alternative drug or class?+
Imipenem belongs to the carbapenem class, which also includes meropenem and ertapenem. Compared with meropenem, imipenem has a broader spectrum against Pseudomonas aeruginosa but may have a higher risk of seizures, especially in patients with renal dysfunction. Choice depends on local susceptibility patterns and patient factors.
What are the storage and handling requirements for Imipenem E Cilastatina Aurobindo?+
The product must be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Once reconstituted, it should be used within the time frame specified in the product labeling and kept under the same temperature conditions.
How is Imipenem E Cilastatina Aurobindo given or administered?+
Imipenem E Cilastatina Aurobindo is supplied as a sterile powder for injection. It is reconstituted with the appropriate diluent, then administered intravenously over a prescribed infusion period, usually 30 minutes to 1 hour, under aseptic conditions.
What are the most serious risks to watch for while using Imipenem E Cilastatina Aurobindo?+
The most serious adverse events include seizures (particularly in patients with renal impairment or high doses), severe hypersensitivity reactions such as anaphylaxis, Clostridioides difficile‑associated colitis, and acute renal injury. Prompt medical attention is required if any of these occur.
Who should not use Imipenem E Cilastatina Aurobindo?+
Patients with a known hypersensitivity to imipenem, cilastatin, or any carbapenem/β‑lactam antibiotics should avoid this product. Caution is also advised for individuals with a history of seizures, severe renal impairment, or those receiving valproic acid without appropriate monitoring.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Cilastatin Sodium, Imipenem Monohydrate
Route
Intravenous Use
Manufacturer
Eugia Pharma (Malta) Ltd
Origin
EU

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