Product image of Imipenem/Cilastatin Aptapharma (Cilastatin, Imipenem) supplied by GNH India

Imipenem/Cilastatin Aptapharma

Active Ingredient:
Cilastatin, Imipenem
Origin:
EU

Imipenem/Cilastatin Aptapharma (Cilastatin, Imipenem)

Imipenem, the active ingredient in Imipenem/Cilastatin Aptapharma, is a carbapenem antibiotic presented as a powder for solution for injection for intravenous use. It treats serious bacterial infections such as complicated intra‑abdominal, urinary tract, skin and soft‑tissue, lower respiratory tract infections and febrile neutropenia in hospitalized patients.

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

Manufacturer / TM Owner

Apta Medica Internacional D.O.O.

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Indications & Clinical Uses

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

  • Complicated intra‑abdominal infections: effective bacterial eradication in patients with perforated or postoperative abdominal infections.
  • Complicated urinary tract infections: clears resistant Gram‑negative pathogens in acute pyelonephritis and cystitis.
  • Skin and soft tissue infections: treats severe cellulitis, necrotizing fasciitis, and infected wounds.
  • Lower respiratory tract infections: combats pneumonia caused by multidrug‑resistant organisms.
  • Febrile neutropenia: provides rapid coverage for high‑risk neutropenic patients with suspected bacterial sepsis.

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, blocks renal dehydropeptidase I, preventing enzymatic degradation of imipenem and thereby extending its plasma concentration and antibacterial activity.

Side Effects

Imipenem/cilastatin may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Nausea: transient gastrointestinal discomfort.
  • Diarrhea: may be mild to moderate.
  • Headache: occasional dull or throbbing pain.
  • Rash: erythematous skin eruption.
  • Elevated liver enzymes: mild transaminase increase.
  • Injection site reactions: pain or erythema at the infusion site.

Serious or Rare Side Effects

  • Seizures: especially in patients with renal impairment or high doses.
  • Anaphylaxis: severe allergic reaction with hypotension and airway compromise.
  • Clostridioides difficile‑associated diarrhea: potentially life‑threatening colitis.
  • Thrombocytopenia: marked reduction in platelet count.
  • Acute renal impairment: sudden decrease in kidney function.
  • Pseudomembranous colitis: inflammation of the colon due to toxin‑producing bacteria.

Precautions & Warnings

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

  • Renal function: adjust dose in patients with impaired renal clearance.
  • Seizure risk: monitor patients with central nervous system disorders or receiving high doses.
  • Allergy: avoid in individuals with known hypersensitivity to β‑lactam antibiotics.
  • Drug interactions: review concomitant medications that may lower seizure threshold.
  • Pregnancy and lactation: prescribe only when the potential benefit justifies the potential risk.
  • Store at 2‑8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Imipenem/cilastatin can interact with several medicines; clinicians should evaluate the relevance of each.

Major Interactions (Avoid)

  • Valproic acid: may reduce serum levels, increasing seizure risk.
  • Ganciclovir: antagonistic effect reducing antiviral efficacy.
  • Probenecid: can raise imipenem concentrations, heightening toxicity.

Moderate Interactions (Monitor Closely)

  • Diuretics: may alter renal clearance of the drug.
  • Aminoglycosides: additive nephrotoxic potential.
  • Anticonvulsants (e.g., phenobarbital): may lower seizure threshold when combined.

Frequently Asked Questions

Imipenem/Cilastatin is indicated for serious bacterial infections such as complicated intra‑abdominal infections, complicated urinary tract infections, skin and soft‑tissue infections, lower respiratory tract infections, and febrile neutropenia. It is typically reserved for hospitalized patients where broad‑spectrum coverage is required.

Imipenem inhibits bacterial cell‑wall synthesis by binding to penicillin‑binding proteins, preventing peptidoglycan cross‑linking and causing cell lysis. Cilastatin is co‑administered to inhibit renal dehydropeptidase I, which would otherwise degrade imipenem, thereby prolonging its antibacterial activity.

The dosage of Imipenem/Cilastatin is individualized and set by the prescribing clinician based on the type and severity of infection, renal function, and patient weight. Dosing regimens may vary from multiple daily infusions to extended‑infusion schedules.

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. Breastfeeding mothers should consult their healthcare provider before treatment.

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 similar to meropenem and doripenem but includes cilastatin to protect against renal degradation, allowing higher plasma concentrations. Choice among carbapenems often depends on local resistance patterns, dosing convenience, and specific safety profiles such as seizure risk.

Imipenem/Cilastatin powder for injection should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Once reconstituted, the solution should be used promptly according to the manufacturer’s instructions and discarded if not used within the recommended time.

The product is supplied as a sterile powder for solution for injection. After reconstitution with the appropriate diluent, it is administered intravenously, usually over 30 minutes to 1 hour, depending on the clinical protocol and patient condition.

The most serious adverse events include seizures, especially in patients with renal impairment or high doses; severe hypersensitivity reactions such as anaphylaxis; and Clostridioides difficile‑associated colitis, which can lead to life‑threatening diarrhea and colonic inflammation.

Patients with a known hypersensitivity to imipenem, cilastatin, or any β‑lactam antibiotics should avoid this medication. Caution is also advised for individuals with severe renal impairment who cannot be dose‑adjusted, and for those with a history of seizures unless benefits outweigh risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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