Plant origin allergen extracts (plant pollen)
House dust mite allergen extracts
Allergen extract mixtures
Sublingual solution
10 IR/ml; 300 IR/ml
Specific immunotherapy medicine. It is used in patients allergic to plant origin allergens (plant pollen) or house dust mites, whose list is attached to this leaflet.
Allergic diseases of a seasonal or year-round nature, manifested by rhinitis (sneezing, runny nose or itchy nose, stuffy nose), conjunctivitis (itchy and watery eyes) or asthma (mild or moderate) in adults and children (over 5 years old).
The goal of treatment with STALORAL 300 is to increase immunological tolerance to allergens, thereby alleviating allergic reactions.
Only a doctor can determine if there are contraindications to the use of the medicine.
Before starting treatment, symptoms of allergy should be stabilized with appropriate symptomatic treatment, if necessary.
Before starting treatment with STALORAL 300, inform your doctor or pharmacist:
Tell your doctor about all medicines you have taken recently, including those available without a prescription.
Before starting treatment, inform your doctor:
Symptomatic treatment (e.g., antihistamines and/or nasal corticosteroids) may be used concurrently with STALORAL 300.
Pregnant women, or women who think they may be pregnant, or are planning to become pregnant, should consult a doctor or pharmacist before using this medicine.
Breastfeeding women should consult a doctor or pharmacist before using this medicine.
There is no experience with the use of STALORAL 300 in pregnant or breastfeeding women, so immunotherapy should not be started in pregnant or breastfeeding women unless the doctor considers it necessary.
Women who become pregnant or start breastfeeding during treatment with STALORAL 300 should consult a doctor about continuing to take this medicine.
There are no contraindications to driving or using machines during treatment with STALORAL 300.
In the case of patients on a low-sodium diet, the presence of sodium chloride in the medicine should be taken into account (one 10 ml vial contains 590 mg of sodium chloride). See "Warnings and Precautions".
STALORAL 300 should always be used in accordance with the doctor's recommendations. In case of doubts, consult a doctor or pharmacist again. In case of using a higher dose of STALORAL 300 than recommended or missing a dose of STALORAL 300,
read the information in the relevant sections of the leaflet.
Specific immunotherapy is most effective when started in the early stages of the disease.
The dose size does not depend on age, but on the degree of individual patient reactivity.
In the case of seasonal allergies, it is recommended to start treatment before the pollen season and continue until the end of the pollen season.
In the case of year-round allergies, it is recommended to continue treatment throughout the year.
Treatment is divided into two stages:
In treatment, allergen solutions of different concentrations are used, for which the packaging differs in cap color:
Cap color: blue - concentration 10 IR/ml
Cap color: purple - concentration 300 IR/ml
The dose of the medicine should be measured under the tongue by pressing the pump dispenser and after 2 minutes should be swallowed.
The medicine is used daily, with each dose increased until the maintenance dose is reached according to the following scheme:
First week | Second week | ||||
Concentration: 10 IR/ml | Concentration: 300 IR/ml | ||||
Day | number of presses | Dose (IR) | Day | number of presses | Dose (IR) |
1 2 3 4 5 | 1 2 3 4 5 | 2 4 6 8 10 | 6 7 8 9 | 1 2 3 4 | 60 120 180 240 |
The above dosing scheme should be considered as a guideline and example of treatment. Treatment can be modified depending on the patient's condition and their reaction to treatment.
The maximum well-tolerated dose should be taken daily or three times a week.
The recommended dosing of the medicine is at least 4 presses 3 times a week or 2 to 4 presses taken daily, using a solution with a concentration of 300 IR/ml.
Clinical trials with the use of STALORAL 300 with various allergens have shown that a daily dose of 300 IR is well tolerated.
Usually, desensitization treatment is used for a period of 3 to 5 years.
The doctor will reassess the treatment in case of no significant improvement in symptoms after a year (year-round allergy) or after the first pollen season (seasonal allergy).
To ensure the safe use of the medicine, the doctor's recommendations should be strictly followed.
STALORAL 300 is administered sublingually.
Before taking the medicine, carefully check the information on the packaging and make sure it matches the doctor's prescription (recipe): patient's name, composition and concentration of the medicine, as well as check the expiry date of the medicine.
The medicine should be taken during the day, to an empty stomach, without food and drink.
The dose of the medicine should be measured under the tongue by pressing the pump dispenser and after 2 minutes should be swallowed.
The doctor may recommend a different dosing schedule depending on the patient's condition and their reaction to treatment.
STALORAL 300 should be administered to children by adults.
Instructions for the First Use of the Medicine:
During the first use, follow the points below:
Usually, desensitization treatment is used for 3 to 5 years. In the case of seasonal allergies, specific immunotherapy can be carried out for several seasons in subsequent years.
Allergen immunotherapy is not recommended for children under 5 years old.
Tell your doctor or pharmacist immediately.
In the case of using a higher dose of the medicine than recommended, the risk of side effects increases.
Do not take a double dose to make up for a missed dose.
Treatment should be continued the next day, taking the established dose.
If the medicine is discontinued for less than a week, treatment can be continued using the last dose. If treatment is interrupted for more than a week, consult a doctor.
In case of any further doubts about the use of this medicine, consult a doctor, pharmacist, or nurse.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
During treatment with STALORAL 300, the patient will be exposed to the action of substances that can cause allergic reactions at the injection site and/or symptoms that can affect the whole body.
Such reactions may occur at the start of treatment or later, during treatment.
Severe allergic reaction with rapid onset of symptoms, which affects the whole body, e.g., intense itching or rash, difficulty breathing, abdominal pain, or symptoms related to low blood pressure, such as dizziness, malaise.
Tolerance to a given dose may change over time depending on the patient's health and environment.
In case of side effects, consult a doctor, who may change the treatment schedule.
The doctor may prescribe pre-treatment with antiallergic medicines to reduce the frequency and severity of side effects.
Common (affects less than 1 in 10 patients)
Mouth disorders (e.g., swelling, discomfort, tingling, itching, numbness, blisters, ulcers), tongue swelling, discomfort in the throat or pain or swelling or irritation,
rhinitis (stuffy nose, runny nose, sneezing, itchy nose, discomfort in the nose), cough,
salivary gland disorders, itchy eyes, itchy ears, nausea, vomiting, abdominal pain, diarrhea, redness or itching of the skin.
Uncommon (affects less than 1 in 100 patients)
Eye disorders (redness, irritation of the eyes, watery eyes), herpes, hoarseness, breathing difficulties, asthma, hives, atypical skin allergy symptoms (burning, tingling, pricking), gastritis, esophageal spasms.
Rare (affects less than 1 in 1000 patients)
Headache, eczema, joint pain, muscle pain, weakness, enlarged lymph nodes (glands), fever.
The following side effects have also been reported:
Taste disorders, dry mouth, dizziness, facial swelling, severe allergic reactions, esophagitis.
If you experience any side effects, including those not listed in this leaflet, tell your doctor, pharmacist, or nurse. Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products, Medical Devices, and Biocidal Products, Al. Jerozolimskie 181C, 02-222 Warsaw, tel. 22 49 21 301, fax 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 help to gather more information on the safety of the medicine.
The medicine should be stored out of sight and reach of children.
Before opening: Store in a refrigerator (2°C - 8°C).
After opening:
10 IR/ml: Store in a refrigerator (2°C - 8°C) for up to 30 days.
300 IR/ml: Store at a temperature below 25°C for up to 30 days or in a refrigerator (2°C - 8°C) for up to 30 days.
During transport, vials should always be carried in an upright position.
Do not use this medicine for more than 30 days after opening and after the expiry date stated on the carton after the "EXP" date. The expiry date refers to the last day of the given month.
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 the medicine is allergen extracts or their mixtures with a concentration of 10 or 300 IR/ml (according to annex 1) in combination with mannitol. The amount of mannitol does not exceed 40 mg/ml.
The qualitative composition of the active substance may be individually selected for the patient within the range of allergens listed in annex 1.
The activity of the relevant allergen expressed in IR units/ml is indicated on the label.
* IR (reactivity index): the allergen extract has an activity equal to 100 IR/ml if it causes a wheal with a diameter of 7mm in a prick test using a Stallerpoint needle in 30 people allergic to the given allergen.
Additionally, the sensitivity of the tested persons is confirmed by a positive reaction to 9% sodium chloride or 10 mg/ml histamine dihydrochloride in a prick test.
Other ingredients are: sodium chloride, glycerol, purified water
Basic treatment set:
3 vials of 10 ml (concentration 10 IR/ml, concentration 300 IR/ml, concentration 300 IR/ml)
+ 3 pump dispensers
Maintenance treatment set:
2 vials of 10 ml (concentration 300 IR/ml, concentration 300 IR/ml)
+ 2 pump dispensers
STALLERGENES
6, rue Alexis de Tocqueville
92160 Antony, France
To obtain more detailed information, contact the representative of the marketing authorization holder in Poland:
STALLERGENES Sp. z o.o.
tel. 22 620 29 98
Date of last update of the leaflet: 02/2024
ANNEX 1
661Timothy grass (Phleum pratense)
609Black alder (Alnus glutinosa)
615White birch (Betula alba)
651European olive (Olea europea)
649Hazel (Corylus avellana)
315Dermatophagoides pteronyssinus
314Dermatophagoides farinae
6885 grasses (meadow fescue, sweet vernal grass, perennial ryegrass, meadow grass, timothy grass)
350Dermatophagoides pteronyssinus, Dermatophagoides farinae
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