Bilastinum
This medicine should always be taken exactly as described in this package leaflet for the patient or as directed by a doctor or pharmacist.
Bilastyna Hitaxa contains the active substance bilastine, which has antihistamine properties.
Bilastyna Hitaxa is used in adults and in adolescents 12 years of age and older to relieve symptoms of hay fever (sneezing, itching, runny nose, and nasal congestion, as well as red and itchy eyes) and other forms of allergic rhinitis. The medicine may also be used to treat itchy skin rashes (hives).
If there is no improvement after 3 days or the patient feels worse, they should consult their doctor.
Before taking Bilastyna Hitaxa, the patient should discuss it with their doctor or pharmacist if they have moderate to severe kidney problems, low potassium, magnesium, or calcium levels in the blood, if they have or have had heart rhythm problems or a very slow heart rate, if they are taking medicines that may affect heart rhythm, if they have or have had an abnormal heart rhythm (known as a prolonged QTc interval on an electrocardiogram), which can occur in certain types of heart disease, and also if the patient is taking other medicines (see "Bilastyna Hitaxa and other medicines").
Do notexceed the recommended dose.
The patient should tell their doctor or pharmacist about all medicines they are taking, have recently taken, or might take, including those obtained without a prescription.
In particular, the patient should inform their doctor or pharmacist if they are taking any of the following medicines:
Do nottake this medicine with food or with grapefruit juice or other fruit juices, as this reduces the effect of Bilastyna Hitaxa. To avoid reducing the effect of the medicine, the patient should:
Bilastine at the recommended dose (20 mg) does not increase drowsiness caused by alcohol consumption.
There are no data or limited data on the use of bilastine in pregnant women, during breastfeeding, and on fertility.
If the patient is pregnant or breastfeeding, thinks they may be pregnant, or plans to have a baby, they should consult their doctor before taking this medicine.
The doctor will decide whether Bilastyna Hitaxa can be taken during pregnancy and breastfeeding.
It has been shown that taking bilastine at a dose of 20 mg does not affect the ability to drive vehicles in adults. However, the response to treatment may vary from patient to patient.
Therefore, before driving or operating machinery, the patient should check their reaction to the medicine.
This medicine should always be taken exactly as described in this package leaflet for the patient or as directed by a doctor or pharmacist. If the patient has any doubts, they should consult their doctor or pharmacist.
The recommended dose for adults, including the elderly, and adolescents 12 years of age and older is 1 tablet (20 mg) per day.
Consult a doctorif there is no improvement after 3 days or if the patient feels worse.
The duration of treatment depends on the type of disease and is determined by the doctor.
This medicine should not be given to children under 12 years of age.
In case of overdose, the patient should immediately contact a doctor or pharmacist or go to the emergency department of the nearest hospital. They should take the medicine packaging or leaflet with them.
Do nottake a double dose to make up for a missed dose.
If a dose is missed, the patient should take the missed dose as soon as possible and then continue taking the medicine at the usual time.
If the patient has any further doubts about taking this medicine, they should consult their doctor or pharmacist.
Like all medicines, Bilastyna Hitaxa can cause side effects, although not everybody gets them.
If the patient experiences symptoms of an allergic reaction (frequency not known), including difficulty breathing, dizziness, fainting, or loss of consciousness, swelling of the face, lips, tongue, or throat, and (or) swelling and redness of the skin, they should stop taking the medicine and consult their doctor immediately.
Frequency not known: cannot be estimated from the available data
If the patient experiences any side effects, including any side effects not listed in the leaflet, they should tell their doctor or pharmacist, or nurse. 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:
Al. Jerozolimskie 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, more information can be collected on the safety of the medicine.
The medicine should be stored out of sight and reach of children.
Do not use this medicine after the expiry date stated on the carton and blister after "EXP".
The expiry date refers to the last day of the month.
There are no special precautions for storage.
Medicines should not be disposed of via wastewater or household waste. The patient should ask their pharmacist how to dispose of medicines no longer required. This will help protect the environment.
Bilastyna Hitaxa tablets are white, round, and 7 mm in diameter.
The tablets are packaged in PA/Aluminum/PVC/Aluminum blisters.
Pack sizes: 10 or 20 tablets.
Not all pack sizes may be marketed.
Adamed Pharma S.A.
Pieńków, ul. Mariana Adamkiewicza 6A
05-152 Czosnów
phone: +48 22 732 77 00
Adamed Pharma S.A.
ul. Marszałka Józefa Piłsudskiego 5
95-200 Pabianice
NOUCOR HEALTH, S.A.
Avda. Camí Reial 51-57
08184 Palau-Solità i Plegamans (Barcelona)
Spain
Date of last revision of the leaflet:04.2025
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