Package Insert: Information for the Patient
Ibis 20 mg Tablets
Bilastine
Read this entire package insert carefully before starting to take this medication, as it contains important information for you.
Ibis contains bilastine as the active ingredient, which is an antihistamine. Ibis is used to relieve symptoms of allergic rhinoconjunctivitis (runny nose, nasal itching, nasal discharge, nasal congestion, and red, watery eyes) and other forms of allergic rhinitis. It may also be used to treat skin eruptions with itching (hives or urticaria).
Do not take Ibis
If you are allergic to bilastine or any of the other components of this medication (listed in section 6).
Warnings and precautions
Consult your doctor or pharmacist before starting to use Ibis if you have moderate or severe renal insufficiency, low blood levels of potassium, magnesium, calcium, if you have or have had heart rhythm problems or if your heart rate is very low, if you are taking medications that may affect heart rhythm, if you have or have had a certain abnormal pattern of your heartbeat (known as QTc interval prolongation in the electrocardiogram) that may occur in some types of heart disease and you are also taking other medications (see “Use of Ibis with other medications”).
Children
Do not administer this medication to children under 12 years of age
Do not exceed the recommended dose. If symptoms persist, consult your doctor.
Use of Ibis with other medications
Inform your doctor or pharmacist if you are using, have used recently or may need to use any other medication, including those purchased without a prescription.
Particularly, please consult with your doctor if you are taking any of the following medications:
Taking Ibis with food, drinks, and alcohol
These tabletsshould not be taken withfoodor withgrapefruit juice or other fruit juices, as this would decrease the effect of bilastine. To avoid this, you can:
Bilastine, at the recommended dose (20 mg), does not increase the drowsiness caused by alcohol.
Pregnancy, breastfeeding, and fertility
There are no data, or these are limited, on the use of bilastine in pregnant women, during lactation, or on its effects on fertility.
If you are pregnant or breastfeeding, think you may be pregnant, or intend to become pregnant, consult your doctor or pharmacist before using this medication.
Consult your doctor or pharmacist before using any medication.
Driving and operating machinery
Bilastine 20 mg has been shown not to affect performance during driving in adults. However, the response of each patient to the medication may be different. Therefore, check how this medication affects you before driving or operating machinery.
Ibis contains sodium
This medication contains less than 1 mmol of sodium (23 mg) per tablet; this is, essentially “sodium-free”.
Follow exactly the administration instructions for this medication as indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
The recommended dose in adults, including elderly patients and adolescents 12 years of age or older, is 1 tablet (20 mg) per day.
Regarding the duration of treatment, your doctor will determine the type of disease you have and will indicate for how long you should take Ibis.
Use in children
For children 6 to 11 years of age with a minimum body weight of 20 kg, there are other more suitable pharmaceutical forms – bilastine 10 mg chewable tablets or bilastine 2.5 mg/mL oral solution –, consult your doctor or pharmacist.
Do not administer bilastine to children under 6 years of age with a body weight less than 20 kg since there are not enough data available.
If you take more Ibis than you should
If you, or anyone else, exceed the dose of this medication, inform your doctor immediately or go to the nearest hospital emergency service. Please remember to bring this medication package or this leaflet with you.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicological Information Service, phone: 91 562 04 20 (indicating the medication and the amount ingested).
If you forget to take Ibis
Do nottake a double dose to compensate for a missed dose.
If you forget to take your dose, take it as soon as possible, and then return to your usual dosing schedule.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medicines, this medicine may cause side effects, although not everyone will experience them.
If you experience allergic reactions whose symptoms may include difficulty breathing, dizziness, fainting, or loss of consciousness, swelling of the face, lips, tongue, or throat, and/or swelling and redness of the skin, stop taking this medicine and seek immediate medical attention.
Other side effects that may occur in adults and adolescents are:
Frequent: may affect up to 1 in 10 people
Rare: may affect up to 1 in 100 people
?electrocardiogram changes
Unknown frequency: cannot be estimated from available data
Side effects that may appear in children:
Frequent: may affect up to 1 in 10 people
Rare: may affect up to 1 in 100 people
Reporting of side effects
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through the Spanish System for Pharmacovigilance of Medicines for Human Use:www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears after CAD on the packaging and blister. The expiration date is the last day of the month indicated.
This medication does not require special storage conditions.
Medications should not be disposed of through drains or trash.Deposit the packaging and medications you no longer need at the Sigre Point of your pharmacy.Ask your pharmacist if you are unsure how to dispose of the packaging and medications you no longer need. By doing so, you will help protect the environment.
Appearance of the product and contents of the package
Ibis tablets are white, oval, biconvex, and scored (length 10 mm, width 5 mm).
The tablets are packaged in blisters of 10, 20, 30, 40, or 50 tablets.
Only some package sizes may be commercially available.
Marketing Authorization Holder
Menarini International Operations Luxembourg, S.A.
1, Avenue de la Gare
L-1611 Luxembourg
Local Representative
Laboratorios Menarini, S.A.
Alfons XII, 587 – E 08918 Badalona (Barcelona)
Responsible for manufacturing
Faes Farma, S.A.
Máximo Aguirre, 14
48940 – Leioa
Spain
or
A.Menarini Manufacturing Logistics and Services S.r.l.
Campo di Pile
L’Aquila
Italy
or
Menarini - Von Heyden GmbH
Leipziger Strasse 7-13; 01097
Dresden
Germany
This medicine is authorized in the member states of the European Economic Area and in the United Kingdom (Northern Ireland)with the following names:
Austria: Olisir 20 mg Tablets
Belgium: Bellozal 20 mg Tablet
Bulgaria: Fortecal 20 mg
Cyprus: Bilaz 20 mg
Czech Republic: Xados
Denmark: Revitelle20 mg tablets
Estonia: Opexa
Finland: Revitelle 20 mg tablets
France: Bilaska 20 mg Compressed Tablet
Germany: Bilaxten 20 mg Tablets
Greece: Bilaz 20 mg
Hungary: Lendin 20 mg tablet
Iceland: Bilaxten 20 mgtablets
Ireland: Drynol 20 mg tablets
Italy: Bysabel 20 mg Compressed Tablet
Latvia: Opexa 20 mg tablets
Lithuania: Opexa 20 mg tablets
Luxembourg: Bellozal 20 mg Tablet
Malta: Gosall 20 mg tablets
Norway: Zilas 20 mg tablets
Poland: Clatra
Portugal: Lergonix 20 mg Compressed Tablet
Romania: Borenar 20 mg tablets
Slovakia: Omarit
Slovenia: Bilador 20 mg tablets
Spain: Ibis 20 mg tablets
Sweden: Bilaxten 20 mg tablets
United Kingdom (Northern Ireland): Ilaxten 20 mg tablets
Last review date of this leaflet:April 2025
Further information on this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es/
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