Product image of Kolneb (Colistimethate Sodium) supplied by GNH India

Kolneb

Active Ingredient:
Colistimethate Sodium
Origin:
EU

Kolneb (Colistimethate Sodium)

Colistimethate Sodium, the active ingredient in Kolneb, is a Polymyxin antibiotic presented as an inhalation for inhalation use. It treats chronic Pseudomonas aeruginosa lung infection in cystic fibrosis patients.

GNH India supplies Kolneb as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies, clinics and research institutions worldwide.

Manufacturer / TM Owner

Teva Nederland B.V.

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Indications & Clinical Uses

Kolneb is a polymyxin antibiotic used to manage chronic bacterial airway infections in cystic fibrosis.

  • Chronic Pseudomonas aeruginosa lung infection in cystic fibrosis: reduces bacterial burden and helps preserve lung function.
  • Persistent airway colonisation by Pseudomonas aeruginosa in cystic fibrosis: aids in long‑term suppression of the pathogen.
  • Multidrug‑resistant Gram‑negative respiratory infections in cystic fibrosis: provides an alternative option when other agents fail.

How It Works

  • Colistimethate Sodium binds to lipopolysaccharides and phospholipids in the outer membrane of Gram‑negative bacteria, especially Pseudomonas aeruginosa. This interaction disrupts membrane integrity, increases permeability, and leads to leakage of cellular contents, ultimately causing bacterial cell death.

Side Effects

Kolneb may cause a range of adverse reactions, most of which are related to its local pulmonary administration and systemic absorption.

Common Side Effects

  • Cough: irritation of the airways may provoke a persistent cough.
  • Bronchospasm: transient narrowing of the bronchial tubes can occur during inhalation.
  • Throat irritation: patients often report soreness or a burning sensation in the throat.
  • Taste disturbance: a metallic or salty taste is frequently noted.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Respiratory failure: marked decline in breathing function, especially in vulnerable patients.
  • Nephrotoxicity: systemic absorption can impair kidney function.
  • Ototoxicity: potential hearing loss or balance disturbances, particularly with high cumulative exposure.

Precautions & Warnings

Before prescribing Kolneb, clinicians should evaluate patient‑specific risk factors and monitor for potential complications.

  • Renal function monitoring: assess serum creatinine and eGFR regularly due to possible nephrotoxicity.
  • Auditory assessment: perform baseline and periodic hearing tests to detect ototoxic effects.
  • Bronchospasm risk: pre‑treat with bronchodilators in patients with reactive airway disease.
  • Hepatic impairment: use caution in patients with cystic fibrosis‑related liver disease.
  • Store at room temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Colistimethate Sodium can interact with several drug classes, influencing safety and efficacy.

Major Interactions (Avoid)

  • Neuromuscular blocking agents (e.g., vecuronium): increased risk of muscle weakness and respiratory compromise.
  • Aminoglycosides (e.g., gentamicin): additive nephrotoxicity and ototoxicity.

Moderate Interactions (Monitor Closely)

  • Loop diuretics (e.g., furosemide): may enhance renal toxicity; monitor renal parameters.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): potential for increased kidney injury; assess renal function.
  • Rifampin: may reduce colistin plasma levels, diminishing efficacy; consider therapeutic drug monitoring.

Frequently Asked Questions

Kolneb is an inhaled formulation of colistimethate sodium indicated for the treatment of chronic Pseudomonas aeruginosa lung infection in patients with cystic fibrosis. It is designed to deliver the antibiotic directly to the airways, helping to reduce bacterial load and support lung function.

Colistimethate sodium binds to lipopolysaccharides and phospholipids in the outer membrane of Gram‑negative bacteria. This binding disrupts membrane integrity, increases permeability, and leads to leakage of cellular contents, ultimately causing bacterial cell death.

The specific dose and treatment schedule for Kolneb are determined by the prescribing clinician based on the patient’s age, weight, severity of infection, and pulmonary function. Healthcare providers tailor the regimen to achieve optimal therapeutic effect while minimizing risk.

The safety of colistimethate sodium in pregnancy and lactation has not been definitively established. It should be used only if the potential benefit justifies any potential risk to the fetus or infant, and the decision should be made by a qualified healthcare professional.

To order Kolneb, 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 any cold‑chain requirements) and necessary import documentation.

Kolneb delivers colistimethate sodium directly to the lungs, offering higher local concentrations than systemic antibiotics and reducing systemic exposure. Compared with intravenous colistin, inhalation can achieve effective airway levels with a lower risk of systemic nephrotoxicity, making it a preferred option for chronic airway infection in cystic fibrosis.

Kolneb should be stored at room temperature, below 25 °C, in its original packaging. Protect the product from moisture and direct sunlight. Do not freeze. Before use, ensure the inhalation device is clean and follow the manufacturer’s instructions for reconstitution or preparation if required.

Kolneb is administered by inhalation using a nebulizer or a compatible inhalation device as directed by the prescriber. The patient inhales the aerosolized solution, allowing the drug to reach the lower respiratory tract. Proper technique and device maintenance are essential for optimal delivery.

The most serious risks include anaphylactic reactions, respiratory failure, nephrotoxicity, and ototoxicity. Patients should be monitored for signs of allergic response, changes in kidney function, hearing loss, or worsening respiratory status, and the drug should be discontinued if severe adverse events occur.

Kolneb is contraindicated in individuals with a known hypersensitivity to colistimethate sodium or any component of the formulation. It should also be avoided in patients with severe renal impairment where systemic absorption could exacerbate kidney injury, unless the prescriber determines the benefits outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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