Package Insert: Information for the Patient
Ebastel Forte 20 mg Film-Coated Tablets
ebastina
Read this package insert carefully before taking this medicine, as it contains important information for you.
Ebastel Forte belongs to a group of medications called antihistamines (antiallergics).
Ebastel Forte is indicated for the treatment of symptoms of allergic processes such as seasonal or perennial allergic rhinitis associated or not with allergic conjunctivitis (such as runny nose, nasal itching, eye itching, tearing, urge to sneeze), chronic urticaria and allergic dermatitis.
Consult your doctor or pharmacist before starting to take Ebastel Forte.
This medication should be used with caution:
Do not use this medication if you are experiencing an acute allergic emergency, as ebastine (active ingredient of this medication) takes 1 to 3 hours to take effect.
Children
Ebastel Forte should not be administered to children under 12 years of age. In this group of patients, Ebastel 1 mg/ml Oral Solution is recommended.
Other medications and Ebastel Forte
Inform your doctor or pharmacist that you are taking, have taken recently, or may need to take any other medication.
The following medications may interact with Ebastel Forte; in these cases, it may be necessary to adjust the dose or discontinue treatment with one of them:
No interactions have been described between ebastine and theophylline, warfarin, cimetidine, diazepam, and alcohol.
Interference with diagnostic tests
Ebastel Forte may interfere with the results of skin allergy tests, so it is recommended not to perform them until 5-7 days after discontinuing treatment.
Taking Ebastel Forte with food and drinks
The tablets can be taken with or without food.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, or think you may be pregnant, consult your doctor or pharmacist before using this medication.
Pregnancy
There is no experience in pregnant women, so it is recommended to consult a doctor before taking Ebastel Forte. They will decide whether to start treatment or not.
Breastfeeding
It is unknown whether the medication passes into breast milk, so it should not be used during breastfeeding.
Driving and operating machinery
In men, no effects have been observed on psychomotor function, or on the ability to drive or operate machinery, at the recommended therapeutic doses. However, given that drowsiness and dizziness are among the adverse effects, observe your response to the medication before driving or operating machinery.
Ebastel Forte contains lactose
This medication contains lactose. If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medication.
This medication contains less than 23 mg of sodium (1 mmol) per tablet; that is, it is essentially "sodium-free".
Follow exactly the administration instructions for this medication as indicated by your doctor. If in doubt, consult your doctor or pharmacist again.
Remember to take your medication.
Your doctor will indicate the duration of your treatment with Ebastel Forte.
Dosage
Use in adults and children over 12 years:The usual dose is 10 mg of ebastine once a day, although some patients may require a dose of 20 mg once a day.
Use in patients with severe liver disease:Do not exceed a dose of 10 mg of ebastine per day. In this case, it is recommended to use the 10 mg presentation (Ebastel 10 mg Coated Tablets).
Administration Form
This medication is for oral administration.
The tablets can be taken with or without food, with the help of a glass of water.
If you estimate that the action of Ebastel Forte is too strong or too weak, inform your doctor or pharmacist.
If you take more Ebastel Forte than you should
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately, call the Toxicological Information Service, phone 915 620 420 (indicating the medication and the amount ingested) or go to the nearest hospital. Bring the remaining tablets, the box, and the complete packaging so that the healthcare staff can identify the medication you have taken more easily.
The treatment of intoxication by this medication consists of gastric lavage and administration of the appropriate medication.
Do not take a double dose to compensate for the missed doses. Take the missed dose when you remember and then continue with your usual schedule. However, if there are only a few hours left before the next dose, do not take the missed dose and wait for the next dose at the scheduled time.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medications, Ebastel Forte can produce adverse effects, although not all people may experience them.
In clinical trials and post-marketing experience, the following adverse effects have been observed:
Very common (may affect more than 1 in 10 people):
Common (may affect up to 1 in 10 people):
Rare (may affect up to 1 in 1,000 people):
Unknown frequency (cannot be estimated from available data):
Reporting Adverse Effects
If you experience any type of adverse effect, consult your doctor, pharmacist, or nurse, even if it is a possible adverse effect not listed in this prospectus. You can also report them directly through the Spanish System for Pharmacovigilance of Medicinal Products for Human Use: https://www.notificaram.es. By reporting adverse effects, you can contribute to providing more information on the safety of this medication.
Keep this medication out of the sight and reach of children.
Do not store at a temperature above30°C.
Do not use this medication after the expiration date that appears on the packaging after CAD. The expiration date is the last day of the month indicated.
Medicines should not be disposed of through drains or in the trash.Deposit the packaging and medications you no longer need at the SIGRE collection pointof the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need.This will help protect the environment.
Composition of Ebastel Forte
Appearance of the product and contents of the packaging
Ebastel Forte is presented in the form of coated tablets with a film for oral administration, conditioned in PVC/Aluminum blisters. The tablets areround, white in color, and have one face marked with E20.
Each package contains 20 coated tablets.
Holder of the marketing authorization and responsible for manufacturing
Holderof the marketing authorization
Almirall, S.A.
General Mitre, 151
08022 - Barcelona (Spain)
Responsible for manufacturing
Industrias Farmacéuticas Almirall, S.A.
Ctra. de Martorell, 41-61
08740 Sant Andreu de la Barca - Barcelona (Spain)
Date of the last review of this leaflet: May 2019
The detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es/
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