Standardized allergen extract of grass pollen from timothy grass (Phleum pratense)
Grazax contains an allergen extract from grass pollen. Grazax is used to treat hay fever and allergic conjunctivitis caused by grass pollen in adults and children (5 years of age and older).
Grazax relieves allergy symptoms by increasing immune tolerance to grass pollen.
Children should be qualified for treatment by doctors who have experience in treating allergic diseases in children.
The doctor will assess the allergic symptoms and perform skin tests or order a blood test to decide if Grazax should be used.
It is recommended to take the first sublingual lyophilisate in the presence of a doctor. This precaution allows for the assessment of the patient's individual sensitivity to treatment and discussion with the doctor of possible side effects.
Grazax is prescribed by doctors with experience in treating allergies.
Before starting treatment with Grazax, discuss with your doctor:
Some side effects can be severe and require immediate medical attention.
Symptoms, see section 4.
If any of the above situations occur, consult your doctor before taking Grazax.
There is a lack of experience with the use of Grazax in the elderly (65 years of age or older).
Tell your doctor or pharmacist about all medicines you are taking or have recently taken, including those obtained without a prescription. If you are taking other allergy medicines, such as antihistamines or corticosteroids, your doctor should assess the use of such medicines.
Do not eat or drink anything for 5 minutes after taking the sublingual lyophilisate.
Currently, there are no data on the use of Grazax during pregnancy. Do not start treatment with Grazax during pregnancy. If you become pregnant during treatment, consult your doctor about whether to continue treatment.
Currently, there is no experience with the use of Grazax during breastfeeding. It is not expected to affect the breastfed baby.
The patient is responsible for assessing their ability to drive or perform precision work. The effects or symptoms of the medicine may affect this ability. The description of these effects is presented in other sections of this package leaflet. Therefore, read all the information in this package leaflet before driving or operating machinery.
In case of doubts, consult your doctor or pharmacist again.
Treatment with Grazax has no significant effect on the ability to drive and use machines.
Always take this medicine exactly as your doctor has told you. If you are not sure, ask your doctor or pharmacist.
The first dose of Grazax should be taken in a doctor's office, because:
Take Grazax every day, even if it takes some time before the symptoms improve.
If the allergy symptoms do not improve during the first grass pollen season, consult your doctor to discuss continuing treatment.
Before touching the medicine, make sure your hands are dry.
If you take too many Grazax sublingual lyophilisates, you may experience allergy symptoms, including local symptoms in the mouth and throat. If the symptoms are severe, seek medical attention immediately.
If you miss a sublingual lyophilisate, take it later that day. Do not take a double dose in one day to make up for the missed dose.
The condition for the effectiveness of the treatment is to take the medicine as recommended by your doctor.
If you have any further questions about taking this medicine, ask your doctor or pharmacist.
Like all medicines, Grazax can cause side effects, although not everybody gets them.
A side effect can be an allergic reaction to the allergen being treated.
In most cases, side effects last from a few minutes to a few hours after taking the sublingual lyophilisate and disappear within one week of starting treatment.
Stop taking Grazax and tell your doctor or go to the hospital immediately if you experience any of the following symptoms:
If you experience persistent heartburn, consult your doctor.
Very common (may affect more than 1 in 10 people):
Common (may affect up to 1 in 10 people):
Uncommon (may affect up to 1 in 100 people):
Rare (may affect up to 1 in 1000 people):
In children, eye irritation, throat redness, mouth blisters, ear pain, and ear swelling are more common than in adults.
If you experience troublesome side effects, consult your doctor, who will determine whether it is necessary to administer anti-allergic medicines, such as antihistamines.
If you experience any side effects, including any not listed in this package leaflet, please tell your doctor or pharmacist.
Side effects can be reported directly to the Department of Post-Marketing Surveillance of Medicinal Products, Medical Devices, and Biocidal Products, Al. Jerozolimskie 181 C, 02-222 Warsaw, Tel.: +48 22 49 21 301, Fax: + 48 22 49 21 309, website: https://smz.ezdrowie.gov.pl
Side effects can also be reported to the marketing authorization holder.
Reporting side effects will allow for more information to be collected on the safety of the medicine.
Keep out of sight and reach of children.
Do not use this medicine after the expiry date stated on the blister and carton after the term "Expiry date" or "EXP". The expiry date refers to the last day of the month.
There are no special precautions for the storage of the medicinal product.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
The active substance of Grazax is a standardized allergen extract from grass pollen from timothy grass (Phleum pratense).The activity of the medicine is expressed in SQ-T* units per sublingual lyophilisate.
The activity of one sublingual lyophilisate is 75,000 SQ-T units. One sublingual lyophilisate contains 6 micrograms of Phl p 5 allergen.
* (Standardised Quality units Tablet (SQ-T) – standardized quality unit of the tablet)
The other ingredients of the medicine are: gelatin (from fish), mannitol, and sodium hydroxide.
Round, white to off-white sublingual lyophilisate, marked with an embossed image on one side.
Aluminum blisters with a removable aluminum foil in an outer cardboard box. Each blister contains 10 sublingual lyophilisates. The following pack sizes are available: 30 (3 x 10), 90 (9 x 10), or 100 (10 x 10) sublingual lyophilisates.
Not all pack sizes may be marketed.
ALK-Abelló A/S
Bøge Allé 6-8
DK-2970 Hørsholm
Denmark
ALK-Abelló S.A.
Miguel Fleta 19
28037 Madrid
Spain
Date of last revision of the package leaflet:19.12.2024
Need help understanding this medicine or your symptoms? Online doctors can answer your questions and offer guidance.