Prospecto: information for the patient
Yasnal 10 mg film-coated tablets EFG
hydrochloride of donepezil
Read this prospectus carefully before starting to take this medication, as it contains important information for you.
-This medication has been prescribed only to you, and you should not give it to others even if they have the same symptoms as you, as it may harm them.
1.What is Yasnal and for what it is used
2.What you need to knowbefore starting to take Yasnal
3.How to take Yasnal
4.Possible adverse effects
6.Contents of the package and additional information
Yasnal (donepezil hydrochloride) contains the active ingredient donepezil hydrochloride. Yasnal (donepezil hydrochloride) belongs to a group of medicines called acetylcholinesterase inhibitors. Donepezil increases the levels in the brain of a substance related to memory (acetylcholine), by decreasing the rate of breakdown of this substance.
It is used for the treatment of symptoms of dementia in people who have been diagnosed with mild to moderately severe Alzheimer's disease. These symptoms include memory loss, confusion, and changes in behavior. As a result, patients with Alzheimer's find it increasingly difficult to carry out their normal daily activities.
Yasnal is used only in adults.
Do not take Yasnal
Warnings and precautions
Consult your doctor or pharmacist before starting to take Yasnal if you have or have had:
Also, consult your doctor if you are pregnant or think you may be pregnant.
Children and adolescents
Yasnal is not recommended for use in children and adolescents (under 18 years of age).
Other medications and Yasnal
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication, including medications obtained without a prescription. Also, include medications you may take in the future if you continue to take Yasnal. The reason is that these medications may increase or decrease the effect of Yasnal.
Especially, it is important to inform your doctor if you are taking any of the following medications:
If you are going to undergo a surgical procedure that requires general anesthesia, you must inform your doctor and anesthesiologist that you are taking Yasnal. The reason is that this medication may affect the amount of anesthesia needed.
Yasnal can be used in patients with kidney disease or mild to moderate liver disease. Inform your doctor if you have kidney or liver disease. Patients with severe liver disease should not take Yasnal.
Inform your doctor or pharmacist of the name of your caregiver. This person will help you take the medication as prescribed.
Taking Yasnal with food, drinks, and alcohol
Food does not affect the effect of Yasnal.
Yasnal should not be taken with alcohol because alcohol may modify its effect.
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, or think you may be pregnant, consult your doctor or pharmacist before using this medication.
If you are breastfeeding, do not take this medication.
Driving and operating machinery
Alzheimer's disease may affect your ability to drive or operate machinery and should not engage in these activities unless your doctor tells you it is safe to do so.
Additionally, this medication may cause fatigue, drowsiness, and muscle cramps. If you experience any of these effects, do not drive or operate machinery.
Yasnal contains lactose
If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medication.
Follow exactly the administration instructions of this medication indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
Amount of Yasnal you should take
The initial recommended dose is 5 mg (one white tablet) each night.
If you have abnormal dreams, nightmares, or difficulty sleeping (see section 4), your doctor may recommend that you take this medication in the morning.
After a month of treatment, your doctor may increase your dose to one 10 mg tablet (one yellow tablet) each night.
Your dose may vary depending on the time you have been taking this medication and what your doctor recommends. The maximum recommended dose is 10 mg each night.
Always follow the advice of your doctor or pharmacist on how much and when to take your medication. Do not alter this dose without consulting your doctor.
How to take your medication
Swallow your Yasnal tablet with a glass of water before going to bed.
Use in children and adolescents
Yasnal is not recommended for use in children and adolescents (under 18 years old).
If you take more Yasnal than you should
Contact your doctor or the nearest hospital emergency service immediately if you take more medication than you should. Carry this leaflet and your remaining tablets with you at all times.
The symptoms of overdose may include nausea (feeling unwell) and vomiting (disease), drooling, sweating, slow heart rate, decreased blood pressure (mild headache or dizziness when standing up), difficulty breathing, fainting, and convulsions.
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 forgot to take Yasnal
If you forget to take your medication, take the next dose at your usual time. Do not take a double dose to compensate for the missed dose.
If you forget to take your medication for more than a week, call your doctor before taking any more tablets.
If you interrupt treatment with Yasnal
Do not stop taking the tablets unless your doctor tells you to. If you stop taking Yasnal, the benefits of treatment will decrease gradually.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
How long should you take Yasnal
Your doctor or pharmacist will advise you on how long you should continue taking the tablets. You will need to see your doctor from time to time to review your treatment and evaluate your symptoms.
Like all medicines, this medicine may cause side effects, although not everyone will experience them.
The following side effects have been reported with Yasnal.
Inform your doctor if you experience any of these side effects while taking Yasnal.
Severe side effects:
If you observe any of the severe side effects, inform your doctor immediately. You may need urgent medical treatment.
Unknown frequency
Other side effects
Very common side effects(may affect more than 1 in 10 people):
Common side effects(may affect up to 1 in 10 people):
Uncommon side effects(may affect up to 1 in 100 people):
Rare side effects(may affect up to 1 in 1,000 people):
Unknown frequency (cannot be estimated from available data):
Reporting 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 theSpanish 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.
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Keep this medication out of the sight and reach of children.
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.
This medication does not require special storage precautions.
Medications should not be disposed of through drains or in the trash. Dispose of packaging and medications you no longer need at the SIGRE collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of packaging and medications you no longer need. By doing so, you will help protect the environment.
Composition of Yasnal
Each film-coated tablet contains 10 mg of donepezil hydrochloride (as monohydrate) equivalent to 9.12 mg of donepezil.
See section 2 "Yasnal contains lactose."
Appearance of the product and contents of the package
The film-coated tablets of 10 mg are light brown, round, biconvex, approximately 9 mm in diameter.
Yasnal 10 mg is available in packages containing:
It may only be marketed in some package sizes.
Marketing Authorization Holder:
KRKA, d.d., Novo mesto, Šmarješka cesta 6, 8501 Novo mesto, Slovenia
Responsible for manufacturing:
KRKA, d.d., Novo mesto, Šmarješka cesta 6, 8501 Novo mesto, Slovenia
O
TAD Pharma GmBH, Heinz Lohmann strasse, 5 - Groden Cuxhaven - D-27472 - Germany
You can request more information about this medication by contacting the local representative of the marketing authorization holder:
KRKA Farmacéutica, S.L., C/ Anabel Segura 10, 28108 Alcobendas, Madrid, Spain
This medication is authorized in the member states of the European Economic Area and in the United Kingdom (Northern Ireland) with the following names:
Member state name | Medication name |
Germany, Bulgaria, Slovakia, Spain, Italy, Hungary, Czech Republic, Romania | Yasnal |
Greece | Donepezil/Krka |
Austria, Belgium, Cyprus, Denmark, France, Finland, Ireland, Sweden, Norway | Donepezil Krka |
Portugal | Donepezilo Krka |
United Kingdom (Northern Ireland) | Donepezil hydrochloride |
Last review date of this leaflet: : December 2022
The detailed information about 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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