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Ibis 20 mg comprimidos

О препарате

Introduction

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.

  • Keep this package insert, as you may need to refer to it again.
  • If you have any questions, consult your doctor or pharmacist.
  • This medication has been prescribed only for you and should not be given to others, even if they have the same symptoms as you, as it may harm them.
  • If you experience any adverse effects, consult your doctor or pharmacist, even if they are not listed in this package insert. See section 4.
  1. What Ibis is and for what it is used
  2. What you need to know before starting to take Ibis
  3. How to take Ibis
  4. Possible adverse effects
  5. Storage of Ibis
  6. Contents of the package and additional informationl

1. What is Ibis and how is it used

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).

2. What you need to know before starting to take Ibis

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:

  • Ketoconazole (an antifungal medication)
  • Erythromycin (an antibiotic)
  • Diltiazem (to treat angina pectoris)
  • Ciclosporin (to reduce the activity of your immune system, to prevent transplant rejection or reduce the activity of autoimmune diseases and allergic disorders, such as psoriasis, atopic dermatitis or rheumatoid arthritis)
  • Ritonavir (to treat HIV)
  • Rifampicin (an antibiotic)

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:

  • take the tablet and wait one hour before eating or taking fruit juices, or
  • if you have eaten food or fruit juices, wait for two hours before taking the tablet.

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”.

3. How to Take Ibis

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.

  • The tablet is to be taken orally.
    • The tablet should be taken one hour before or two hours after taking any food or fruit juice (see section 2, “Taking Ibis with food, drinks, and alcohol”).
    • Swallow the tablet with a glass of water.
    • The groove is only for breaking the tablet if it is difficult to swallow whole.

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.

4. Possible Adverse Effects

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

  • headache
  • drowsiness

Rare: may affect up to 1 in 100 people

?electrocardiogram changes

  • blood tests showing changes in liver function
  • dizziness
  • stomach pain
  • fatigue
  • increased appetite
  • irregular heartbeat
  • weight gain
  • nausea (urge to vomit)
  • anxiety
  • dry or irritated nose
  • abdominal pain
  • diarrhea
  • gastritis (inflammation of the stomach lining)
  • vertigo (a feeling of dizziness or instability)
  • weakness
  • thirst
  • shortness of breath
  • dry mouth
  • indigestion
  • itching
  • herpes labialis
  • fever
  • tinnitus (ringing in the ears)
  • difficulty sleeping
  • blood tests showing changes in kidney function
  • increased blood fats

Unknown frequency: cannot be estimated from available data

  • palpitations (feeling the heartbeat)
  • tachycardia (rapid heartbeat)
  • vomiting

Side effects that may appear in children:

Frequent: may affect up to 1 in 10 people

  • rhinitis (nasal irritation)
  • allergic conjunctivitis (eye irritation)
  • headache
  • stomach pain (abdominal pain/superior abdominal pain)

Rare: may affect up to 1 in 100 people

  • eye irritation
  • dizziness
  • loss of consciousness
  • diarrhea
  • nausea (urge to vomit)
  • swelling of the lips
  • eczema
  • urticaria (hives)
  • fatigue

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.

5. Ibis Conservation

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.

6. Contents of the packaging and additional information

Composition of Ibis

  • The active ingredient is bilastine. Each tablet contains 20 mg of bilastine.
  • The other components are microcrystalline cellulose, sodium carboxymethylstarch type A (derived from potato), anhydrous colloidal silica, magnesium stearate.

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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