Product image of Grazax (Phleum Pratense (225)) supplied by GNH India

Grazax

Active Ingredient:
Phleum Pratense (225)
Origin:
EU

Grazax (Phleum Pratense (225))

Grazax is a prescription sublingual tablet containing 225 µg of Phleum pratense (timothy grass) extract. It is formulated for oral administration under the tongue and is classified as an allergen immunotherapy product for the treatment of grass pollen‑induced allergic rhinitis and seasonal allergic rhinoconjunctivitis in the European market. The medication is intended for use before the grass pollen season and requires a prescription from a qualified healthcare professional.

Manufacturer / TM Owner

Alk-Abello A/S

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Indications & Clinical Uses

Grazax is indicated for patients with documented sensitivity to grass pollen who experience allergic rhinitis or rhinoconjunctivitis symptoms.

  • Initiation of allergen immunotherapy prior to the start of the grass pollen season.
  • Reduction of seasonal nasal congestion, sneezing, and itchy eyes associated with grass pollen exposure.
  • Long‑term disease‑modifying effect that may lessen the need for symptomatic medications.
  • Use in adults and children (typically from age 5) with confirmed grass pollen allergy.
  • Administration as a single daily sublingual tablet under medical supervision.

Side Effects

The safety profile of Grazax includes both frequently observed and less common reactions, most of which are mild and transient.

Common

  • Oral itching or mild irritation of the mouth and throat.
  • Transient throat swelling that resolves without intervention.
  • Mild ear or nasal itching.
  • Slight increase in nasal discharge shortly after dosing.
  • Mild abdominal discomfort or nausea.
  • Transient headache or dizziness.

Serious

  • Persistent or progressive swelling of the lips, tongue, or throat that may affect breathing.
  • Anaphylactic reaction characterized by hives, difficulty breathing, or cardiovascular symptoms.
  • Severe systemic allergic reaction requiring emergency medical care.

Precautions & Warnings

Before prescribing Grazax, clinicians should evaluate patient history and consider specific safety considerations to minimize risk.

  • Confirmed diagnosis of grass pollen allergy through skin testing or specific IgE measurement.
  • Avoid use in patients with uncontrolled asthma or severe chronic respiratory disease.
  • Assess for a history of severe allergic reactions, especially to sublingual or oral immunotherapy.
  • Do not administer to pregnant or breastfeeding individuals unless the benefit outweighs potential risk.
  • Ensure the tablet is placed under the tongue and not swallowed immediately to allow proper absorption.
  • Monitor patients during the first administration for signs of systemic allergic response.

Avoid Interactions

Grazax may interact with other medications or substances that influence immune response or increase the risk of allergic reactions.

Avoid

  • Concurrent use of beta‑blockers, which can mask symptoms of anaphylaxis and complicate emergency treatment.
  • Simultaneous administration of other allergen immunotherapy products targeting the same or different allergens.

Use with caution

  • Antihistamines or corticosteroids may reduce the perception of mild local reactions, potentially delaying recognition of a serious event.
  • Immunosuppressive agents (e.g., systemic steroids, biologics) could alter the efficacy of the immunotherapy.
  • Vaccinations, particularly live vaccines, should be spaced appropriately from Grazax dosing.

Frequently Asked Questions

Grazax contains a standardized extract of Phleum pratense (timothy grass) at a strength of 225 µg. The sublingual exposure induces immune tolerance by promoting regulatory T‑cell activity and IgG4 antibody production, which reduces the allergic response to grass pollen.

Grazax is prescribed for individuals with confirmed grass pollen allergy who experience allergic rhinitis or rhinoconjunctivitis. Eligibility typically includes adults and children aged five years and older, provided they have no contraindications such as uncontrolled asthma.

The tablet is placed under the tongue once daily, usually starting several weeks before the anticipated grass pollen season. The exact start date and duration are determined by the prescribing clinician based on local pollen patterns.

Yes, Grazax may be prescribed for children who are at least five years old, provided they have a documented grass pollen allergy and meet other safety criteria established by their healthcare provider.

Common reactions include mild oral itching, transient throat swelling, ear or nasal itching, slight increase in nasal discharge, mild abdominal discomfort, and occasional headache or dizziness. These effects are usually short‑lived.

Medical attention is warranted if the patient experiences persistent swelling of the lips, tongue, or throat, difficulty breathing, hives, or any signs of anaphylaxis. Prompt evaluation is essential for serious systemic reactions.

Grazax should not be used in individuals with uncontrolled asthma, severe chronic respiratory disease, a history of severe systemic allergic reactions to sublingual immunotherapy, or in pregnant or breastfeeding women unless the benefit clearly outweighs potential risks.

Beta‑blockers can mask the symptoms of anaphylaxis and make emergency treatment more difficult. Concurrent use with Grazax is generally avoided to reduce this risk.

Antihistamines and nasal steroids may be used alongside Grazax, but they can diminish the perception of mild local reactions, potentially delaying recognition of a serious event. Clinicians often advise monitoring when these agents are combined.

The initial administration is usually performed under medical supervision, with observation for at least 30 minutes to detect any immediate systemic allergic response.

Treatment generally continues throughout the grass pollen season and may be repeated annually. The exact duration is individualized based on the patient’s response and the prescribing physician’s recommendation.

The safety of Grazax in pregnancy or while breastfeeding has not been definitively established. Use is only considered if the potential benefit justifies any possible risk to the fetus or infant.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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