For use in adults, adolescents, and children over 5 years old.
An extract of allergens from the pollen of the following grasses:
Common couch grass ( Dactylis glomerataL.), Sweet vernal grass ( Anthoxanthum odoratumL.), Perennial ryegrass ( Lolium perenneL.), Meadow grass ( Poa pratensisL.) and Timothy grass ( Phleum pratenseL.)
ORALAIR contains an allergen extract. The treatment with ORALAIR aims to increase immunological tolerance to grass pollen and thus reduce allergy symptoms.
ORALAIR is used to treat grass pollen allergy, which is characterized by rhinitis (sneezing, runny or itchy nose, stuffy nose) with or without conjunctivitis (itchy and watery eyes) in adults, adolescents, and children over 5 years old.
Before starting treatment, the doctor will diagnose the allergy (hypersensitivity) using a suitable skin test and/or blood test.
Before starting treatment with ORALAIR, you should discuss with your doctor:
ORALAIR is used to treat grass pollen allergy, which is characterized by rhinitis with or without conjunctivitis in adults, adolescents, and children over 5 years old.
ORALAIR is not indicated for use in children under 5 years old.
You should tell your doctor or pharmacist about all medicines you are taking or have recently taken, as well as any medicines you plan to take, including those available without a prescription.
You should inform your doctor in particular if you are taking certain antidepressants (tricyclic antidepressants and monoamine oxidase inhibitors (MAOIs)).
Patients taking other anti-allergic medicines, such as antihistamines, asthma medicines, steroids, or medicines that block the substance called immunoglobulin E (IgE), e.g., omalizumab, should discuss with their doctor the continuation of these medicines. Stopping these anti-allergic medicines may cause further side effects during treatment with ORALAIR. During therapy with ORALAIR, symptomatic treatment (e.g., antihistamines and/or nasal corticosteroids) may be used.
You should inform your doctor or pharmacist before taking ORALAIR: if you are taking medicines that block beta-adrenergic receptors (i.e., a group of medicines often prescribed for heart disorders and high blood pressure, as well as found in some eye drops or ointments), as they may reduce the effectiveness of adrenaline used to treat severe systemic reactions.
You should not eat or drink for 5 minutes after taking this medicine.
If you are pregnant or think you may be pregnant, or if you plan to become pregnant, you should consult your doctor or pharmacist before taking this medicine.
There is no experience with the use of ORALAIR during pregnancy. Therefore, immunotherapy should not be started if you are pregnant. If you become pregnant during treatment, you should discuss with your doctor whether to continue treatment.
Before taking this medicine, you should consult your doctor or pharmacist.
Immunotherapy should not be started during breastfeeding.
There is no experience with the use of ORALAIR during breastfeeding. No effect on breastfed children is expected during treatment. If you plan to breastfeed during treatment, you should consult your doctor about whether to continue treatment.
No effect of ORALAIR on the ability to drive and use machines has been observed.
ORALAIR contains lactose.
If you have been told that you have an intolerance to some sugars, you should consult your doctor before taking this medicine.
ORALAIR contains sodium.
The medicine contains less than 1 mmol (23 mg) of sodium per tablet, which means it is essentially 'sodium-free'.
This medicine should always be taken exactly as your doctor has told you. If you are not sure, you should ask your doctor or pharmacist.
ORALAIR is prescribed by doctors with appropriate training and experience in the treatment of allergies (hypersensitivity). If the medicine is prescribed for children, it is prescribed by a doctor with appropriate experience in the treatment of children.
It is recommended to take the first tablet under medical supervision. This will allow you to discuss possible side effects with your doctor.
Dosage
Treatment consists of an initial phase (including dose increase over 3 days) and a maintenance phase.
Initial treatment
Treatment with ORALAIR should be started as follows:
IR (Index of Reactivity) expresses activity.
ORALAIR 100 IR is intended for use only during the dose increase period and is not intended for maintenance treatment.
Maintenance treatment
The dose is 300 IR (one tablet) per day until the end of the pollen season.
Method of administration
It is recommended to take the first tablet of ORALAIR under medical supervision. You should remain under medical supervision for at least 30 minutes after taking the first dose of the medicine. This precaution is taken to monitor the reaction to the medicine. It also allows you to discuss possible side effects with your doctor.
The tablet should be placed under the tongue until it is completely dissolved (at least 1 minute), and then swallowed. On the second day of treatment, you should place 2 tablets of 100 IR under the tongue at the same time, and then swallow them after about 1 minute. It is recommended to take the tablet during the day on an empty stomach. For the next 5 minutes, you should not eat or drink anything.
Duration of treatment
Treatment should be started about 4 months before the expected pollen season and should be continued until the end of the pollen season.
There is no experience with the use of ORALAIR in patients over 65 years old.
There is no experience with the use of ORALAIR in children under 5 years old.
There is no experience with the use of ORALAIR in children for more than one pollen season.
Dosage in children and adolescents over 5 years old is the same as in adults.
In case of taking a higher dose of ORALAIR than recommended, allergic symptoms may occur, including local symptoms in the mouth and throat. If severe symptoms occur, you should contact your doctor immediately.
You should not take a double dose to make up for a missed dose.
If treatment with ORALAIR is interrupted for less than a week, you can resume treatment with the same dose as the last one taken.
If treatment is interrupted for more than 7 days, you should consult your doctor about how to continue treatment.
Day 1 | 1 tablet of 100 IR |
Day 2 | 2 tablets of 100 IR at the same time |
Day 3 | 1 tablet of 300 IR |
If the treatment cycle with ORALAIR is interrupted, there may be a lack of further benefits from treatment.
If you have any further questions about the use of this medicine, you should consult your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Patients during treatment with ORALAIR are exposed to substances that can cause local reactions at the site of administration and/or symptoms that can affect the whole body. Local reactions at the site of administration (such as itching in the mouth and throat irritation) can be expected. These reactions usually occur at the beginning of therapy, are temporary, and generally decrease over time.
Treatment should only be resumed on the advice of a doctor.
Very common (affect more than 1 in 10 patients):
Common (affect less than 1 in 10 patients):
Uncommon (affect less than 1 in 100 patients)
Rare (affect less than 1 in 1000 patients)
Frequency not known (cannot be estimated from the available data):
Additionally, esophagitis has been reported.
The number of side effects reported by adults who used ORALAIR during three consecutive pollen seasons decreased in the second and third year of use in a clinical trial.
In children and adolescents taking ORALAIR, the following side effects occurred more frequently than in adults: cough, pharyngitis, lip swelling (very common), oral allergy syndrome, cheilitis, feeling of lumps in the throat, tongue inflammation, ear disorders (common).
Additionally, in children and adolescents, the following side effects have been reported: bronchitis, tonsillitis (common), chest pain (uncommon).
(post-marketing experience, frequency not known):
Asthma worsening, systemic allergic reactions.
If you experience any side effects, including those not listed in the leaflet, you should tell your doctor or pharmacist.
Side effects can be reported directly to the
Department of Drug Safety Monitoring of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products
Jerozolimskie Avenue 181C, 02-222 Warsaw
Phone: +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.
By reporting side effects, you can help provide more information on the safety of this medicine.
Keep out of sight and reach of children.
Do not use this medicine after the expiry date stated on the carton after "EXP" and on the blister after "EXP". The expiry date refers to the last day of that month.
There are no special precautions for storage temperature.
Store in the original package to protect from moisture.
Medicines should not be disposed of via wastewater or household waste. You should ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
The active substance of ORALAIR is an allergen extract from the pollen of the following grasses: Common couch grass ( Dactylis glomerataL.), Sweet vernal grass ( Anthoxanthum odoratumL.), Perennial ryegrass ( Lolium perenneL.), Meadow grass ( Poa pratensisL.) and Timothy grass ( Phleum pratenseL.). One sublingual tablet contains 100 IR or 300 IR.
IR (Index of Reactivity) is a measure of activity and is determined in allergic patients based on a skin test.
The other ingredients are: mannitol (E421), microcrystalline cellulose, sodium croscarmellose, colloidal silica, magnesium stearate, and lactose monohydrate.
Tablets of 100 IR are slightly speckled in white to beige color, with "100" embossed on both sides.
Tablets of 300 IR are slightly speckled in white to beige color, with "300" embossed on both sides.
One small blister contains 3 sublingual tablets of 100 IR and one blister contains 28 sublingual tablets of 300 IR
Tablets are provided in blisters (Alu/Alu) with foil (polyamide/aluminum/PCW). The blister cavities are numbered.
Pack size: 31 sublingual tablets.
STALLERGENES
6 rue Alexis de Tocqueville
92160 ANTONY
France
Phone: +33 (0) 1 55 59 20 00
Fax: +33 (0) 1 55 59 21 68
Austria
Oralair 100 IR + 300 IR Sublingualtabletten
Belgium, Estonia, Germany, Ireland, Italy, Latvia, Luxembourg, Malta, Netherlands, Poland, Portugal, Romania, Slovakia
Oralair 100 IR & 300 IR
Bulgaria, Czech Republic
ORALAIR 100 IR & 300 IR
Croatia
Oralair 100 IR i 300 IR sublingvalne tablete
Denmark, Finland, Sweden, Norway
Aitgrys
France
Oralair 100 IR & 300 IR, comprimé sublingual
Hungary
Oralair 100 IR és 300 IR nyelvatti tabletta
Lithuania
ORALAIR 100 IR & 300 IR poliežuvinés tabletés
Slovenia
Oralair 100 IR in 300 IR podjezične tablete
Spain
ORALAIR INICIO 100 IR/300 IR comprimidos sublinguales
Need help understanding this medicine or your symptoms? Online doctors can answer your questions and offer guidance.