Product image of Maxitrol (Neomycin Sulfate, Polymyxin B Sulfate, Dexamethasone) supplied by GNH India

Maxitrol

Active Ingredient:
Neomycin Sulfate, Polymyxin B Sulfate, Dexamethasone
Origin:
EU

Maxitrol (Neomycin Sulfate, Polymyxin B Sulfate, Dexamethasone)

Neomycin Sulfate, Polymyxin B Sulfate and Dexamethasone, the active ingredients in Maxitrol, are a corticosteroid/antibiotic combination presented as an ophthalmic suspension for ocular use. It treats bacterial and inflammatory eye conditions such as conjunctivitis, allergic reactions and post‑operative inflammation in both adults and children.

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

Manufacturer / TM Owner

Novartis Ireland Limited

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Indications & Clinical Uses

Maxitrol is used to manage ocular infections and inflammation across several common eye conditions.

  • Bacterial conjunctivitis: reduces bacterial load and associated inflammation in infected eyes.
  • Allergic conjunctivitis: alleviates allergic swelling, redness and itching.
  • Post‑operative eye inflammation: controls inflammation and prevents infection after eye surgery.
  • Ocular inflammation (non‑infectious): diminishes swelling, pain and redness in various inflammatory eye disorders.

How It Works

  • Dexamethasone binds glucocorticoid receptors, modulating gene transcription to suppress inflammatory mediators. Neomycin, an aminoglycoside, interferes with bacterial ribosomal function, inhibiting protein synthesis. Polymyxin B binds lipopolysaccharide on gram‑negative bacterial membranes, disrupting integrity and causing cell death. Together, the three agents provide anti‑inflammatory and broad‑spectrum antibacterial activity within the ocular surface.

Side Effects

Common Side Effects

  • Burning or stinging sensation upon instillation.
  • Transient blurred vision.
  • Mild eye irritation or itching.
  • Temporary foreign‑body feeling.
  • Slight eyelid edema.
  • Mild conjunctival redness.

Serious or Rare Side Effects

  • Allergic reaction with swelling, rash or hives.
  • Severe eye pain or worsening redness.
  • Vision loss or sudden decrease in visual acuity.
  • Secondary ocular infection or corneal ulceration.
  • Elevated intra‑ocular pressure leading to glaucoma.
  • Persistent or worsening inflammation despite therapy.

Precautions & Warnings

Before using Maxitrol, consider the following precautions.

  • Confirm bacterial infection: ensure the condition is bacterial before initiating therapy.
  • Avoid viral or fungal eye infections: corticosteroids may exacerbate non‑bacterial pathogens.
  • Monitor intra‑ocular pressure: patients with steroid‑responsive glaucoma need regular pressure checks.
  • Limit duration: do not exceed the prescribed treatment period without medical review.
  • Store at room temperature: keep in the original container, protect from light and moisture.

Avoid Interactions

Maxitrol may interact with other ophthalmic agents.

Major Interactions (Avoid)

  • Systemic corticosteroids: may increase systemic steroid exposure.
  • Contact lens wear: can enhance drug absorption and cause irritation.
  • Concurrent ophthalmic antibiotics: may lead to additive toxicity.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory eye drops: may affect healing response.
  • Anticholinergic eye drops: could reduce tear production and exacerbate dryness.
  • Topical ocular anesthetics: may mask early signs of irritation or infection.

Frequently Asked Questions

Maxitrol is an ophthalmic suspension indicated for the treatment of bacterial conjunctivitis, allergic conjunctivitis, ocular inflammation and post‑operative eye inflammation. It combines an antibiotic and a corticosteroid to address both infection and inflammation in the eye.

Neomycin and polymyxin B act as antibiotics: neomycin inhibits bacterial protein synthesis, while polymyxin B disrupts the cell membrane of gram‑negative bacteria. Dexamethasone is a glucocorticoid that binds intracellular receptors to suppress inflammatory pathways, reducing swelling, redness and pain.

The dosing regimen for Maxitrol is determined by the prescribing clinician based on the specific condition, severity and patient factors. The prescriber will provide instructions on the number of drops, frequency and duration of therapy.

Safety data for Maxitrol in pregnancy and lactation are limited. The decision to use it should be made by a healthcare professional after weighing potential benefits against possible risks to the mother and fetus or infant.

To order Maxitrol, 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 and any necessary import documentation.

Compared with single‑agent antibiotic drops, Maxitrol offers both antibacterial and anti‑inflammatory activity, which can simplify therapy for mixed infections and inflammation. Compared with steroid‑only drops, it adds protection against bacterial contamination, but it also carries the combined safety profile of both drug classes.

Store Maxitrol at room temperature, preferably below 25 °C. Keep the bottle tightly closed, protect it from direct sunlight and moisture, and do not freeze. If the suspension appears discolored or contains particles, discard it and obtain a new supply.

Maxitrol is applied as eye drops. The patient should wash hands, tilt the head back, pull down the lower eyelid, and place the prescribed number of drops into the conjunctival sac. Close the eye gently and avoid blinking excessively for a few seconds to allow absorption.

Serious risks include allergic reactions such as severe eye swelling or rash, secondary ocular infections, corneal ulceration, and a rise in intra‑ocular pressure that can lead to glaucoma. Any sudden worsening of vision or pain should prompt immediate medical evaluation.

Maxitrol should be avoided in patients with known hypersensitivity to any of its components, in viral or fungal eye infections, and in individuals with uncontrolled glaucoma or steroid‑responsive intra‑ocular pressure elevations unless closely monitored by an eye specialist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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