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 an allergen immunotherapy presented as a sublingual tablet for oral use. It is employed to modify the immune response to grass pollen in patients with allergic rhinitis and related conditions.
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 used to modify the immune response to grass pollen, helping to reduce allergic disease burden.

  • Seasonal allergic rhinitis (hay fever): reduces nasal symptoms and the need for rescue medication.
  • Allergic conjunctivitis: alleviates eye itching, redness and tearing associated with grass pollen exposure.
  • Grass‑pollen‑triggered mild asthma: may improve symptom control when used as part of a comprehensive allergy management plan.

How It Works

  • Oralair contains standardized grass‑pollen extracts that are administered sublingually to induce immune tolerance. Repeated exposure promotes a shift from a Th2‑dominant response toward regulatory T‑cell activity, increasing allergen‑specific IgG4 and reducing IgE‑mediated mast cell activation, thereby diminishing allergic inflammation upon natural pollen exposure.

Side Effects

Oralair may cause local and systemic reactions, most of which are mild and transient.

Common Side Effects

  • Oral itching or tingling: mild discomfort in the mouth after administration.
  • Throat irritation: transient soreness or scratchy sensation.
  • Ear pruritus: itching in the ears.
  • Mild gastrointestinal upset: nausea or abdominal discomfort.
  • Local swelling: mild swelling of the oral mucosa.
  • Sneezing or mild nasal congestion.

Serious or Rare Side Effects

  • Anaphylaxis: severe, potentially life‑threatening allergic reaction.
  • Systemic allergic reaction: widespread hives, angioedema, or respiratory distress.
  • Asthma exacerbation: worsening of asthma symptoms.
  • Severe oral mucosal edema: pronounced swelling that may impair breathing.
  • Urticaria: widespread hives.
  • Cardiovascular symptoms: hypotension or tachycardia associated with severe reactions.

Precautions & Warnings

Before initiating Oralair, patients should be evaluated for suitability and monitored for adverse reactions.

  • Contraindication: severe uncontrolled asthma: avoid use in patients with recent exacerbations.
  • History of severe allergic reactions: assess risk before starting therapy.
  • Medical supervision: first dose should be administered under physician observation.
  • Interaction with other allergen extracts: avoid simultaneous use of different sublingual immunotherapies.
  • Pregnancy and breastfeeding: discuss potential risks with a healthcare professional.
  • Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Oralair may interact with other medications or therapies, influencing safety or efficacy.

Major Interactions (Avoid)

  • Beta‑blockers: may mask symptoms of anaphylaxis and complicate emergency treatment.
  • Immunosuppressive agents: can reduce the effectiveness of allergen immunotherapy.
  • Concurrent sublingual immunotherapy with different extracts: increased risk of severe local or systemic reactions.

Moderate Interactions (Monitor Closely)

  • Antihistamines: may mask early signs of an allergic reaction.
  • Systemic corticosteroids: may alter immune response to the extract.
  • Live vaccines: consider timing to avoid overlapping immune activation.
  • ACE inhibitors: monitor for angioedema, though risk is low.
  • NSAIDs: watch for enhanced gastrointestinal irritation.

Frequently Asked Questions

Oralair is a sublingual allergen immunotherapy designed to treat seasonal allergic rhinitis, allergic conjunctivitis, and mild asthma caused by grass‑pollen exposure. By gradually exposing the immune system to standardized grass‑pollen extracts, it helps reduce symptom severity and reliance on rescue medications.

The allergen extract in Oralair contains purified pollen proteins from several grass species. When taken sublingually, it stimulates regulatory immune pathways, increasing allergen‑specific IgG4 antibodies and promoting tolerance while decreasing IgE‑mediated mast cell activation, which lessens allergic inflammation during natural pollen seasons.

The dosing regimen for Oralair is individualized and determined by the prescribing healthcare professional. The prescriber selects the appropriate starting dose, titration schedule, and maintenance dose based on the patient’s age, severity of allergy, and clinical response.

Safety of Oralair in pregnancy or while breastfeeding has not been fully established. Women who are pregnant, planning pregnancy, or nursing should discuss potential risks and benefits with their healthcare provider before initiating therapy.

To order 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 necessary import documentation.

Oralair offers a sublingual route, which can be more convenient than subcutaneous allergy shots that require clinic visits. Compared with antihistamines, it targets the underlying immune response rather than just symptom relief, potentially providing longer‑term disease modification.

Oralair should be stored at room temperature, below 25 °C, in its original packaging. Keep the tablet away from moisture, direct sunlight, and extreme temperatures to maintain product stability.

Oralair is taken as a sublingual tablet placed under the tongue and allowed to dissolve completely without swallowing. The first dose is usually administered under medical supervision, after which patients can continue the regimen at home as directed by their clinician.

The most serious risks include systemic allergic reactions such as anaphylaxis, severe asthma exacerbations, and widespread urticaria or angioedema. Patients should be monitored closely, especially during the initial dosing period, and have emergency medication available if needed.

Oralair is contraindicated in individuals with severe uncontrolled asthma, a history of severe systemic allergic reactions to grass pollen extracts, or those who are unable to comply with the sublingual administration protocol. Consultation with a qualified healthcare professional is essential before starting therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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