Product image of Oralair (Allergen Extract From Pollen Of Dactylis Glomerata, Anthoxanthum Odoratum, Lolium Perenne, Poa Prate) supplied by GNH India

Oralair

Active Ingredient:
Allergen Extract From Pollen Of Dactylis Glomerata, Anthoxanthum Odoratum, Lolium Perenne, Poa Prate
Origin:
EU

Oralair (Allergen Extract From Pollen Of Dactylis Glomerata, Anthoxanthum Odoratum, Lolium Perenne, Poa Prate)

Allergen Extract From Pollen Of Dactylis Glomerata, Anthoxanthum Odoratum, Lolium Perenne, Poa Prate, the active ingredient in Oralair, is a allergen immunotherapy presented as a sublingual tablet for oral use. It is indicated for the treatment of grass‑pollen allergic rhinoconjunctivitis in patients five years of age and older. Oralair is marketed in the European Union and complies with EU regulatory standards for allergen extracts.

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

Manufacturer / TM Owner

Stallergenes

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Indications & Clinical Uses

Oralair is an allergen immunotherapy tablet that targets the immune response to grass‑pollen allergens. It is used to modify disease activity in seasonal allergic conditions.

  • Grass‑pollen allergic rhinitis: reduces nasal congestion, sneezing and itching.
  • Grass‑pollen allergic conjunctivitis: alleviates eye redness, tearing and irritation.
  • Combined allergic rhinoconjunctivitis: improves overall symptom control during the grass pollen season.

How It Works

  • Oralair delivers standardized grass‑pollen allergen extracts to the oral mucosa, where they are taken up by antigen‑presenting cells. Repeated exposure induces regulatory T‑cell responses and a shift from IgE‑mediated to IgG4‑mediated immunity, promoting long‑term tolerance and reducing the clinical reactivity to grass pollen.

Side Effects

Common Side Effects

  • Oral itching or tingling: mild irritation of the mouth and throat.
  • Throat irritation: transient soreness after tablet placement.
  • Ear pruritus: itching in the ear canal.
  • Nasal congestion: mild blockage of nasal passages.
  • Cough: brief coughing episodes after administration.
  • Mild gastrointestinal discomfort: occasional stomach upset.

Serious or Rare Side Effects

  • Anaphylaxis: severe, potentially life‑threatening allergic reaction.
  • Systemic allergic reaction: widespread hives, swelling or respiratory difficulty.
  • Severe asthma exacerbation: worsening of asthma symptoms.
  • Angioedema: rapid swelling of lips, tongue or face.
  • Cardiovascular symptoms: dizziness, hypotension or fainting.
  • Persistent gastrointestinal bleeding: rare but serious GI upset.

Precautions & Warnings

Before initiating Oralair, patients should be evaluated for appropriate diagnosis and suitability.

  • Medical evaluation: confirm grass‑pollen allergy and rule out contraindications.
  • Age restriction: not recommended for children younger than five years.
  • Asthma control: ensure asthma is well‑controlled before use.
  • Pregnancy and lactation: discuss risks with a healthcare professional.
  • Concomitant immunotherapy: avoid simultaneous use of other allergen immunotherapies.
  • Store at room temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Oralair may interact with other medicines that affect allergic responses.

Major Interactions (Avoid)

  • Beta‑blockers: can mask symptoms of anaphylaxis and complicate emergency treatment.
  • ACE inhibitors: may increase the risk of severe allergic reactions.

Moderate Interactions (Monitor Closely)

  • Antihistamines: may reduce local side effects but do not eliminate the need for monitoring.
  • Systemic corticosteroids: could alter immune tolerance development.
  • Other allergen immunotherapies: combined use may raise the chance of systemic reactions.

Frequently Asked Questions

Oralair is a sublingual tablet containing standardized grass‑pollen allergen extracts. It is used to treat and reduce symptoms of grass‑pollen allergic rhinoconjunctivitis in patients five years of age and older, helping to lessen nasal, ocular and respiratory complaints during the pollen season.

The allergen extract is placed under the tongue where it is absorbed by immune cells in the oral mucosa. Repeated exposure shifts the immune response toward regulatory T‑cells and IgG4 antibodies, decreasing IgE‑mediated reactivity and building long‑term tolerance to grass pollen.

The dosing schedule for Oralair is individualized by the prescribing clinician based on the patient’s age, allergy severity and response to therapy. The prescriber determines the initial dose, titration steps and maintenance regimen according to the product’s labeling and clinical guidelines.

Safety data for Oralair in pregnancy and lactation are limited. Women who are pregnant, planning pregnancy or breastfeeding should discuss potential risks and benefits with their healthcare provider before starting therapy.

To request Oralair, 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 import documentation.

Oralair is a sublingual immunotherapy, offering a non‑injectable alternative to traditional subcutaneous allergy shots. It provides a convenient at‑home administration route and aims for disease‑modifying effects, whereas antihistamines and nasal corticosteroids only relieve symptoms without inducing long‑term tolerance.

Oralair tablets should be stored at room temperature, below 25 °C, in the original blister pack. Keep the product away from moisture, direct sunlight and excessive heat to maintain potency throughout its shelf life.

The tablet is placed under the tongue and allowed to dissolve completely without swallowing or chewing. Patients should remain upright for at least 30 minutes after administration and avoid eating or drinking during that time to ensure optimal absorption.

The most serious risks include systemic allergic reactions such as anaphylaxis, severe asthma exacerbations, and angioedema. Patients should be educated to recognize early signs of these reactions and have immediate access to emergency medical care if they occur.

Oralair is contraindicated in individuals with uncontrolled asthma, a history of severe systemic allergic reactions to grass‑pollen extracts, those taking beta‑blockers or ACE inhibitors without medical supervision, and children younger than five years of age.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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