GNH USA

Europe — EMA

Imipenem/Cilastatin Hikma

GNH USA supplies Imipenem/Cilastatin Hikma (Imipenem and cilastatin), a carbapenem antibiotic for abdominal infections, pneumonia, sepsis. Request a quote.

Cilastatin Sodium, Imipenem Monohydrate

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What is Cilastatin Sodium, Imipenem Monohydrate?

Imipenem and cilastatin, the active ingredient in Imipenem/Cilastatin Hikma, is a carbapenem antibiotic presented as an injectable solution for intravenous use. It treats a range of serious bacterial infections in adult and pediatric patients when directed by a healthcare professional.

GNH USA supplies Imipenem/Cilastatin Hikma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres and pharmacies worldwide. The company adheres to stringent quality standards and provides regulatory documentation for global distribution.

What is Cilastatin Sodium, Imipenem Monohydrate used for?

Imipenem/Cilastatin is indicated for severe bacterial infections affecting various organ systems.

- Complicated intra‑abdominal infections: eradication of susceptible pathogens causing peritonitis and intra‑abdominal sepsis. - Complicated urinary tract infections: treatment of infections caused by resistant Gram‑negative organisms. - Skin and soft‑tissue infections: management of serious cellulitis, abscesses and wound infections. - Community‑acquired and hospital‑acquired pneumonia: therapy for severe pneumonic infections due to susceptible bacteria. - Severe sepsis and septic shock: broad‑spectrum coverage in critically ill patients with systemic infection.

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

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

Common Side Effects: - Nausea or vomiting - Diarrhea, including mild colitis - Headache - Rash or mild skin irritation - Infusion site pain or phlebitis

Serious or Rare Side Effects: - Seizures, especially in patients with CNS disorders - Anaphylaxis or severe allergic reactions - Clostridioides difficile‑associated colitis - Acute renal dysfunction - Thrombocytopenia or neutropenia - Elevated liver enzymes or hepatitis

What precautions apply to Cilastatin Sodium, Imipenem Monohydrate?

Use Imipenem/Cilastatin with caution in specific clinical situations.

- Renal function: dose adjustment may be required in patients with impaired renal function. - Seizure risk: monitor patients with pre‑existing central nervous system disorders. - Allergy: avoid in individuals with known hypersensitivity to β‑lactam antibiotics. - Hepatic monitoring: observe liver enzymes during prolonged therapy. - Pregnancy and lactation: use only if the benefit outweighs the potential risk. - Store at 2‑8°C: keep refrigerated, protect from light, do not freeze.

What does Cilastatin Sodium, Imipenem Monohydrate interact with?

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

Major Interactions (Avoid): - Valproic acid: concomitant use may reduce valproate levels and precipitate seizures. - Cimetidine or other renal dehydropeptidase inhibitors: may increase imipenem concentrations, raising toxicity risk. - Probenecid: can decrease renal clearance of imipenem, enhancing exposure.

Moderate Interactions (Monitor Closely): - Diuretics: may increase the risk of nephrotoxicity. - Anticoagulants (e.g., warfarin): monitor INR as antibiotics can affect plasma protein binding. - Other broad‑spectrum antibiotics: assess for additive toxicity or antagonism.

Frequently asked questions

What is Imipenem/Cilastatin Hikma used for?+
Imipenem/Cilastatin Hikma is a carbapenem antibiotic used to treat serious bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, severe skin and soft‑tissue infections, community‑acquired or hospital‑acquired pneumonia, and severe sepsis or septic shock when directed by a qualified prescriber.
How does imipenem work in the body?+
Imipenem inhibits bacterial cell‑wall synthesis by binding to penicillin‑binding proteins, which blocks the final cross‑linking steps of peptidoglycan formation, leading to bacterial lysis. Cilastatin, co‑formulated, blocks renal dehydropeptidase I, preventing enzymatic breakdown of imipenem and preserving its antibacterial activity.
What is the usual dose of Imipenem/Cilastatin Hikma?+
The specific dose and infusion rate are determined by the prescribing clinician based on the type and severity of infection, the patient’s renal function, age, weight and other clinical factors. No standard dosing regimen is provided here; the prescriber sets the appropriate regimen.
Is Imipenem/Cilastatin safe during pregnancy or breastfeeding?+
Safety data for Imipenem/Cilastatin in pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision must be made by the treating healthcare professional.
How do I order Imipenem/Cilastatin Hikma from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed) and the necessary import documentation.
How does Imipenem/Cilastatin compare with other carbapenems?+
Imipenem/Cilastatin offers a broad spectrum of activity similar to other carbapenems such as meropenem or ertapenem, but the addition of cilastatin protects the drug from renal degradation, allowing higher and more stable plasma concentrations. Choice among carbapenems depends on local resistance patterns, dosing convenience, and specific patient factors.
What are the storage and handling requirements for Imipenem/Cilastatin Hikma?+
The product should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen. Once reconstituted, use the solution within the time frame specified in the product label and keep it in the original container to maintain sterility.
How is Imipenem/Cilastatin administered?+
Imipenem/Cilastatin is given by intravenous infusion. The reconstituted solution is diluted in an appropriate compatible IV fluid and administered over a period defined by the prescriber, typically ranging from 15 to 60 minutes depending on the clinical situation.
What are the most serious risks associated with Imipenem/Cilastatin?+
The most serious adverse events include seizures (particularly in patients with CNS disorders or renal impairment), severe allergic reactions such as anaphylaxis, and Clostridioides difficile‑associated colitis. Prompt medical attention is required if any of these symptoms occur.
Who should not receive Imipenem/Cilastatin?+
Patients with a known hypersensitivity to imipenem, cilastatin, or any other β‑lactam antibiotics should not receive this medication. Caution is also advised for individuals with a history of seizures, severe renal impairment, or previous severe allergic reactions to related drugs.
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
Hikma Farmacêutica (Portugal), S.A.
Origin
EU

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