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

Kolelang

Active Ingredient:
Colistimethate Sodium
Origin:
EU

Kolelang (Colistimethate Sodium)

Colistimethate sodium, the active ingredient in Kolelang, is a polymyxin antibiotic presented as a sterile injectable solution for intracerebroventricular and intrathecal use. It treats severe infections caused by susceptible Gram‑negative bacteria, particularly in the central nervous system.

GNH India supplies Kolelang as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

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Indications & Clinical Uses

Kolelang is a polymyxin antibiotic used for serious Gram‑negative bacterial infections affecting the central nervous system.

  • Gram‑negative bacterial meningitis: provides bactericidal activity to eradicate the infection within the cerebrospinal fluid.
  • Post‑neurosurgical CNS infection: helps control resistant Gram‑negative pathogens after surgical procedures.
  • Ventriculitis caused by susceptible organisms: delivers high local concentrations to clear infection in the ventricular system.

How It Works

  • Colistimethate sodium binds to the lipopolysaccharide component of the outer membrane of Gram‑negative bacteria. This interaction displaces calcium and magnesium ions, destabilizing the membrane and increasing its permeability. The resulting loss of barrier function leads to leakage of cellular contents and rapid bacterial cell death, providing a bactericidal effect against susceptible organisms.

Side Effects

Colistimethate sodium may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Headache: mild to moderate pain in the head region.
  • Nausea: feeling of sickness often accompanied by an urge to vomit.
  • Fever: elevated body temperature during treatment.
  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Injection‑site pain: local discomfort at the administration site.
  • Tingling or paresthesia: transient sensory disturbances.

Serious or Rare Side Effects

  • Seizures: convulsive episodes requiring immediate medical attention.
  • Anaphylaxis: severe allergic reaction with airway compromise.
  • Nephrotoxicity: acute kidney injury manifested by rising creatinine.
  • Severe neurotoxicity: profound peripheral neuropathy or encephalopathy.
  • Respiratory paralysis: loss of breathing effort, potentially life‑threatening.
  • Hypersensitivity reactions: rash, urticaria, or angioedema.

Precautions & Warnings

When using Kolelang, several precautions should be observed to minimize risks.

  • Renal function monitoring: assess serum creatinine before and during therapy.
  • Neurological assessment: watch for signs of neurotoxicity.
  • Dosage adjustment in renal impairment: reduce dose as recommended.
  • Avoid concurrent nephrotoxic agents: limit exposure to other kidney‑toxic drugs.
  • Pregnancy and lactation: use only if benefit outweighs risk.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Colistimethate sodium can interact with other medicines, affecting safety or efficacy.

Major Interactions (Avoid)

  • Aminoglycosides: additive nephrotoxicity and neurotoxicity.
  • Loop diuretics: increased risk of kidney injury.
  • Neuromuscular blocking agents: potentiation of respiratory paralysis.

Moderate Interactions (Monitor Closely)

  • Vancomycin: possible additive nephrotoxicity.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may worsen renal function.

Frequently Asked Questions

Kolelang contains colistimethate sodium and is indicated for the treatment of severe infections caused by susceptible Gram‑negative bacteria, especially when these infections involve the central nervous system and require intracerebroventricular or intrathecal administration.

Colistimethate sodium binds to the lipopolysaccharide layer of Gram‑negative bacterial outer membranes, displacing stabilising cations. This disrupts membrane integrity, increases permeability, and leads to leakage of cellular contents, resulting in rapid bacterial cell death.

The dose of Kolelang is determined by the prescribing clinician based on the type and severity of the infection, the patient’s renal function, and the route of administration. Specific dosing regimens are not provided here.

Safety data for colistimethate sodium during 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 a qualified healthcare professional.

To order Kolelang, 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 any required import documentation.

Kolelang delivers colistimethate sodium, the same active component found in other colistin products, but is formulated for direct intracerebroventricular or intrathecal use, allowing higher local concentrations in the CNS. This route can be advantageous for treating resistant Gram‑negative infections that are difficult to reach with systemic therapy.

Kolelang should be stored at 2‑8 °C, kept refrigerated, protected from light, and must not be frozen or shaken. Use aseptic technique during preparation and administration to maintain sterility.

Kolelang is administered by a qualified healthcare professional as a sterile injection directly into the cerebrospinal fluid via the intracerebroventricular or intrathecal route, following aseptic procedures and appropriate dosing calculations.

The most serious risks include severe neurotoxicity (such as seizures or encephalopathy), anaphylactic reactions, acute kidney injury (nephrotoxicity), and respiratory paralysis. Prompt recognition and medical intervention are essential if any of these events occur.

Kolelang should be avoided in patients with known hypersensitivity to colistimethate sodium or other polymyxins, in those with uncontrolled renal failure without dose adjustment, and in individuals receiving neuromuscular blocking agents where respiratory compromise could be exacerbated.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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