GNH USA

Europe — EMA

Kolject

GNH USA supplies Kolject (Colistimethate Sodium), a polymyxin antibiotic for infections caused by susceptible Gram‑negative bacteria.

Colistimethate Sodium

Request sourcing

1
Pack/s

What is Colistimethate Sodium?

Colistimethate Sodium, the active ingredient in Kolject, is a polymyxin antibiotic presented as a sterile solution for intravenous use. It treats infections caused by susceptible Gram‑negative bacteria, including Pseudomonas aeruginosa and Acinetobacter baumannii, in hospitalized patients.

GNH USA supplies Kolject as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Colistimethate Sodium used for?

Kolject (colistimethate sodium) is used to treat infections caused by Gram‑negative bacteria, targeting the bacterial outer membrane.

- Pseudomonas aeruginosa infections: effective therapy for severe hospital‑acquired infections. - Acinetobacter baumannii infections: used when isolates are susceptible to colistin. - Other susceptible Gram‑negative bacterial infections: provides an option for multidrug‑resistant organisms.

What are the side effects of Colistimethate Sodium?

Kolject may cause a range of adverse reactions, from mild to severe.

Common Side Effects: - Nephrotoxicity: reduced kidney function, elevated serum creatinine. - Neurotoxicity: paresthesia, dizziness, headache. - Nausea: mild gastrointestinal upset. - Vomiting: occasional episodes. - Diarrhea: loose stools. - Rash: mild skin irritation.

Serious or Rare Side Effects: - Acute renal failure: severe kidney injury requiring dialysis. - Neuromuscular blockade: respiratory muscle weakness, potentially leading to respiratory failure. - Anaphylaxis: severe allergic reaction with hypotension and airway compromise. - Seizures: rare neurological event. - Hematuria: blood in urine indicating renal damage. - Thrombocytopenia: low platelet count increasing bleeding risk.

What precautions apply to Colistimethate Sodium?

Before initiating Kolject therapy, clinicians should consider several safety measures.

- Renal function monitoring: assess serum creatinine before and during therapy. - Neurotoxicity monitoring: watch for tingling, dizziness, or seizures. - Dose adjustment in renal impairment: reduce dose as needed based on clearance. - Avoid concomitant nephrotoxic drugs: limit use of aminoglycosides, NSAIDs, and loop diuretics. - Pregnancy and lactation: use only if benefits outweigh potential risks. - Store at 2‑8 °C: keep refrigerated, protect from light, do not freeze or shake.

What does Colistimethate Sodium interact with?

Kolject can interact with several medications, requiring careful management.

Major Interactions (Avoid): - Aminoglycosides: additive nephrotoxicity. - Loop diuretics: increased risk of renal injury. - Neuromuscular blocking agents: enhanced neuromuscular blockade.

Moderate Interactions (Monitor Closely): - Vancomycin: potential additive nephrotoxicity. - Non‑steroidal anti‑inflammatory drugs (NSAIDs): increased renal risk. - Radiographic contrast media: heightened nephrotoxicity risk.

Frequently asked questions

What is Kolject used for?+
Kolject contains colistimethate sodium, a polymyxin antibiotic indicated for the treatment of serious infections caused by susceptible Gram‑negative bacteria such as Pseudomonas aeruginosa and Acinetobacter baumannii, especially when other antibiotics are ineffective.
How does colistimethate sodium work?+
Colistimethate sodium binds to lipopolysaccharides and phospholipids in the outer membrane of Gram‑negative bacteria, displacing essential cations. This disrupts membrane integrity, increases permeability, and leads to leakage of cellular contents, ultimately causing bacterial cell death.
What is the usual dose of Kolject?+
The dose of Kolject is individualized by the prescribing clinician based on infection severity, pathogen susceptibility, patient weight, and renal function. Dosage regimens are determined in a hospital setting and adjusted according to therapeutic response and safety monitoring.
Is Kolject safe in pregnancy or breastfeeding?+
Safety data for colistimethate sodium 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 physician.
How do I order Kolject from GNH USA?+
To order Kolject, submit an enquiry on the product page at gnh-usa.com with 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 import documentation.
How does Kolject compare with other polymyxin antibiotics?+
Kolject (colistimethate sodium) is a pro‑drug of colistin, offering similar antibacterial spectrum to polymyxin B but is administered intravenously as a sterile solution. Compared with polymyxin B, colistimethate sodium may have a higher risk of nephrotoxicity, while both share neurotoxic potential; selection depends on clinical context and susceptibility data.
How should Kolject be stored and handled?+
Kolject must be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the vial. Before administration, allow the solution to reach room temperature if required, and inspect for particulate matter or discoloration; discard if any abnormalities are observed.
How is Kolject administered?+
Kolject is given by intravenous infusion under the supervision of a qualified healthcare professional. The infusion rate and duration are determined by the prescribing physician, typically over a period of 30‑60 minutes, with appropriate monitoring of renal function and electrolytes during treatment.
What are the most serious risks to watch for with Kolject?+
The most serious adverse events associated with Kolject include acute renal failure, severe neurotoxicity such as neuromuscular blockade leading to respiratory compromise, and rare hypersensitivity reactions like anaphylaxis. Prompt recognition and discontinuation are essential if these events occur.
Who should not use Kolject?+
Kolject should be avoided in patients with known hypersensitivity to colistimethate sodium or any component of the formulation, and in individuals with pre‑existing severe renal impairment unless dose adjustments are made. Caution is also advised for patients receiving other nephrotoxic or neurotoxic agents.
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
Colistimethate Sodium
Route
Intravenous Use
Manufacturer
Teva Nederland B.V.
Origin
EU

Related products