Product image of Itulazax (Betula Verrucosa (108)) supplied by GNH India

Itulazax

Active Ingredient:
Betula Verrucosa (108)
Origin:
EU

Itulazax (Betula Verrucosa (108))

Betula verrucosa, the active ingredient in Itulazax, is a allergen extract presented as a sublingual preparation for sublingual use. It treats allergic rhinitis and allergic conjunctivitis caused by birch pollen in patients with IgE‑mediated sensitivity.

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

Manufacturer / TM Owner

Alk-Abello A/S

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Indications & Clinical Uses

  • Itulazax is used in allergy immunotherapy to address IgE‑mediated reactions to birch pollen.
  • Allergic rhinitis: reduces nasal congestion, sneezing and itching caused by Betula verrucosa pollen.
  • Allergic conjunctivitis: alleviates eye redness, itching and tearing associated with birch pollen exposure.
  • Seasonal allergic rhinoconjunctivitis: provides sustained symptom control throughout the birch pollen season.

How It Works

  • Sublingual administration of Betula verrucosa extract delivers controlled allergen exposure to oral mucosal immune cells, promoting regulatory T‑cell development and IgG4 blocking antibody production while shifting the Th2‑dominant response toward a tolerant Th1 profile, thereby reducing IgE‑mediated allergic inflammation.

Side Effects

Adverse reactions to Itulazax are generally related to local immune activation in the oral cavity and systemic allergic responses.

Common Side Effects

  • Oral itching: mild irritation of the mouth or throat after dosing.
  • Throat irritation: transient discomfort in the throat.
  • Nasal congestion: temporary blockage of nasal passages.

Serious or Rare Side Effects

  • Anaphylaxis: severe, potentially life‑threatening allergic reaction.
  • Angioedema: swelling of lips, tongue or face.
  • Severe bronchospasm: acute narrowing of airways causing breathing difficulty.

Precautions & Warnings

  • When prescribing Itulazax, clinicians should consider several safety measures.
  • Patient selection: confirm IgE‑mediated Betula verrucosa allergy before initiating therapy.
  • Initial dosing: start with a low sublingual dose under medical supervision.
  • Monitoring: observe for at least 30 minutes after first administration for systemic reactions.
  • Contraindications: avoid in patients with a history of severe anaphylaxis to birch pollen.
  • Pregnancy and lactation: use only if potential benefit justifies potential risk; data limited.
  • Store at ambient temperature: keep below 25°C in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Itulazax may interact with other medications that affect allergic response or immune modulation.

Major Interactions (Avoid)

  • Concurrent use of beta‑blockers: may mask symptoms of anaphylaxis and complicate treatment.
  • ACE inhibitors: increase risk of angioedema during allergic reactions.

Moderate Interactions (Monitor Closely)

  • Antihistamines: may reduce efficacy of sublingual immunotherapy if taken shortly before dosing.
  • Corticosteroids: may alter immune response, requiring dose adjustment.
  • Other allergen extracts: simultaneous administration can increase risk of systemic reactions.

Frequently Asked Questions

Itulazax is a prescription allergen extract containing Betula verrucosa, indicated for the treatment of allergic rhinitis and allergic conjunctivitis caused by birch pollen. It is administered sublingually as part of allergy immunotherapy to reduce symptoms and improve tolerance.

Betula verrucosa extract provides controlled exposure to birch pollen allergens via the sublingual route. This exposure promotes the development of regulatory T cells and IgG4 blocking antibodies, shifting the immune response away from an IgE‑driven Th2 profile toward a more tolerant state, thereby decreasing allergic inflammation.

The dosage of Itulazax is determined individually by a qualified healthcare professional based on the patient’s sensitivity, age, and clinical response. The prescriber selects the appropriate starting concentration and titration schedule, and adjustments are made during follow‑up visits.

Safety data for Itulazax in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision should be made by the prescribing clinician in consultation with the patient.

To place an order, submit an enquiry on the Itulazax 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.

Itulazax delivers the allergen extract sublingually, whereas alternative options may include subcutaneous immunotherapy injections

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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