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 administration. It is used to treat grass‑pollen‑induced allergic rhinitis in patients with confirmed sensitivity.

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

Manufacturer / TM Owner

Stallergenes

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Indications & Clinical Uses

Oralair is an allergen immunotherapy that targets grass‑pollen‑related allergic disease.

  • Grass pollen allergic rhinitis: reduces nasal congestion, sneezing and itching during the grass season.
  • Seasonal allergic rhinoconjunctivitis (grass): improves overall symptom control and quality of life.
  • Grass‑induced allergic asthma (adjunct): may lessen asthma exacerbations linked to grass exposure.

How It Works

  • Oralair contains standardized grass‑pollen allergen extracts that are administered sublingually. Repeated exposure induces immune tolerance by shifting the T‑cell response from a Th2‑dominant profile toward regulatory T‑cells, increasing allergen‑specific IgG4 and decreasing IgE‑mediated mast cell activation, thereby reducing clinical reactivity to grass pollen.

Side Effects

Adverse reactions are generally localized to the oral cavity but can range from mild to severe.

Common Side Effects

  • Oral itching or tingling: mild discomfort in the mouth after dosing.
  • Throat irritation: transient soreness or scratchy sensation.
  • Ear pruritus: itching in the ears or around the jaw.
  • Mild gastrointestinal upset: nausea or mild stomach discomfort.
  • Local swelling of the tongue or lips: transient and self‑limiting.

Serious or Rare Side Effects

  • Anaphylaxis: rapid onset of systemic allergic reaction requiring emergency care.
  • Severe systemic allergic reaction: widespread urticaria, angioedema, or respiratory distress.
  • Asthma exacerbation: worsening of underlying asthma symptoms.
  • Severe oral edema: pronounced swelling that interferes with breathing or swallowing.
  • Cardiovascular collapse: rare but life‑threatening drop in blood pressure.

Precautions & Warnings

Oralair should be used with careful patient selection and monitoring.

  • Contraindication: severe uncontrolled asthma: avoid use until asthma is stable.
  • Pregnancy: limited data, use only if potential benefit outweighs risk.
  • Breastfeeding: no specific studies, consider risk‑benefit before prescribing.
  • Monitoring: observe patients for at least 30 minutes after first dose for systemic reactions.
  • Drug interactions: inform patients about possible interactions with immunosuppressants.
  • Storage: Store at ambient temperature below 25°C: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Oralair may interact with other agents that affect immune response or mask allergic symptoms.

Major Interactions (Avoid)

  • Beta‑blockers: may blunt response to emergency epinephrine during anaphylaxis.
  • Immunosuppressive therapy (e.g., high‑dose steroids, chemotherapy): may reduce efficacy of immunotherapy.

Moderate Interactions (Monitor Closely)

  • Antihistamines: can mask early local reactions, making monitoring harder.
  • Systemic corticosteroids: may alter immune modulation during treatment.
  • Omalizumab (anti‑IgE): may affect the clinical response to allergen extracts.
  • Live vaccines: schedule administration to avoid overlapping immune activation.

Frequently Asked Questions

Oralair is a sublingual allergen immunotherapy tablet designed to treat grass‑pollen‑induced allergic rhinitis and related seasonal rhinoconjunctivitis. It works by gradually desensitizing the immune system to specific grass pollen proteins, reducing symptom severity during the grass season.

The allergen extract contains standardized proteins from several grass species. Repeated sublingual exposure promotes regulatory immune pathways, increases allergen‑specific IgG4 antibodies, and suppresses IgE‑mediated mast cell activation, leading to long‑term tolerance to grass pollen.

The dosing regimen for Oralair is individualized by the prescribing clinician based on the patient’s age, sensitivity profile, and treatment goals. The prescriber determines the starting dose, escalation schedule, and maintenance dose according to approved guidelines.

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

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 tablet, whereas many alternatives are administered via subcutaneous injections. The sublingual route offers the convenience of at‑home dosing and eliminates the need for frequent clinic visits, though both approaches aim to achieve long‑term tolerance to grass pollen.

Oralair tablets should be stored at ambient temperature below 25 °C, in the original packaging, protected from moisture and direct sunlight. Do not refrigerate or freeze the product, and keep it out of reach of children.

Oralair is taken sublingually: the tablet is placed under the tongue and allowed to dissolve completely without swallowing or drinking for at least 30 minutes. Patients should avoid eating or drinking during this period to ensure optimal absorption.

The most serious risks include systemic allergic reactions such as anaphylaxis, severe asthma exacerbations, and pronounced oral or facial swelling that can compromise breathing. Patients should be educated to recognize early signs and seek immediate medical attention if they occur.

Oralair is contraindicated in individuals with severe uncontrolled asthma, a history of life‑threatening systemic allergic reactions to grass pollen, or those receiving beta‑blocker therapy that cannot be discontinued. It should also be used with caution in pregnant or breastfeeding women.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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