Product image of Natriumcromoglicaat Teva (Sodium Cromoglicate) supplied by GNH India

Natriumcromoglicaat Teva

Active Ingredient:
Sodium Cromoglicate
Origin:
EU

Natriumcromoglicaat Teva (Sodium Cromoglicate)

Sodium cromoglicate, the active ingredient in Natriumcromoglicaat Teva, is a mast cell stabilizer presented as an ophthalmic solution for ocular and subconjunctival use. It is used to manage allergic conjunctivitis and to prevent ocular allergic reactions in patients of all ages.

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

Manufacturer / TM Owner

Teva Nederland B.V.

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Indications & Clinical Uses

Sodium cromoglicate acts on ocular allergic pathways to reduce inflammation and symptom severity.

  • Allergic conjunctivitis: alleviates itching, redness, and tearing associated with seasonal or perennial eye allergies.
  • Prophylaxis of ocular allergic reactions: prevents onset of symptoms when patients are exposed to known allergens.
  • Seasonal allergic conjunctivitis: provides pre‑emptive control of eye irritation during high pollen periods.

How It Works

  • Sodium cromoglicate stabilises mast cells in the conjunctival and corneal tissues, inhibiting the release of histamine, leukotrienes, and other inflammatory mediators. By preventing degranulation, it reduces vascular permeability and nerve activation, thereby limiting the ocular allergic response without directly blocking histamine receptors.

Side Effects

Adverse reactions are generally mild and local to the eye.

Common Side Effects

  • Transient ocular burning or stinging at instillation.
  • Mild blurred vision lasting a few minutes.
  • Temporary tearing or watery discharge.
  • Foreign‑body sensation.
  • Mild headache.
  • Conjunctival hyperemia.

Serious or Rare Side Effects

  • Severe allergic reaction (anaphylaxis) with swelling of the eyelids or face.
  • Corneal ulceration or epithelial defect.
  • Persistent eye pain or photophobia.
  • Vision loss or sudden visual acuity change.
  • Severe eyelid edema.
  • Acute intraocular inflammation.

Precautions & Warnings

Before prescribing sodium cromoglicate, clinicians should consider patient‑specific factors and handling requirements.

  • Pregnancy: safety not established; use only if potential benefit justifies the risk.
  • Breastfeeding: unknown excretion in milk; assess risk versus benefit.
  • Pediatric use: safety data limited; monitor closely in children.
  • Contact lens wear: advise removal during treatment and for at least 15 minutes after instillation.
  • Hypersensitivity: discontinue if signs of severe local or systemic allergic reaction appear.
  • Store at room temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Sodium cromoglicate may interact with other ocular or systemic agents, requiring attention to combined effects.

Major Interactions (Avoid)

  • Topical ophthalmic anesthetics: increased risk of corneal toxicity when used concurrently.
  • Systemic antihistamines: may diminish the perceived efficacy of the eye drop.

Moderate Interactions (Monitor Closely)

  • Topical corticosteroids: additive risk of intra‑ocular pressure elevation.
  • Contact lens cleaning solutions: potential incompatibility affecting drug stability.
  • Systemic immunosuppressants: monitor for heightened infection risk due to combined anti‑inflammatory actions.

Frequently Asked Questions

Natriumcromoglicaat Teva contains sodium cromoglicate, a mast cell stabiliser indicated for the treatment of allergic conjunctivitis and for prophylaxis of ocular allergic reactions. It helps reduce itching, redness, and tearing caused by eye allergies.

Sodium cromoglicate stabilises mast cells in the conjunctiva and cornea, preventing the release of histamine, leukotrienes and other inflammatory mediators. By blocking degranulation, it limits the cascade that leads to ocular itching, swelling and redness.

The dosing regimen for Natriumcromoglicaat Teva is determined by the prescribing clinician based on the patient’s condition, severity of symptoms and response to therapy. The product is supplied as an ophthalmic solution for instillation into the affected eye(s).

Safety data for sodium cromoglicate in pregnancy and lactation are limited. It should only be used if the potential benefit outweighs any possible risk to the fetus or infant, and the decision should be made in consultation with a healthcare professional.

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 and any required import documentation.

Unlike antihistamine eye drops that block histamine receptors, sodium cromoglicate stabilises mast cells, preventing the release of multiple inflammatory mediators. This mechanism can provide broader symptom control, especially for patients who do not respond fully to antihistamines alone.

Store the ophthalmic solution at room temperature, below 25 °C, in the original container. Protect it from direct light, moisture and extreme temperature fluctuations to maintain potency and sterility.

The product is applied as eye drops. The prescribed number of drops is instilled into the affected eye(s) using the provided dropper, typically once or twice daily, or as directed by the prescriber. Patients should avoid touching the dropper tip to the eye or any surface.

Serious but rare risks include severe allergic reactions such as anaphylaxis, corneal ulceration, persistent eye pain, sudden loss of vision, and severe eyelid edema. Any of these symptoms require immediate medical attention and discontinuation of the product.

Patients with known hypersensitivity to sodium cromoglicate or any excipients in the formulation should avoid use. Caution is also advised for individuals with active ocular infections, severe ocular surface disease, or those who are pregnant or breastfeeding without a clear benefit‑risk assessment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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