


Ask a doctor about a prescription for DONEPEZIL TECNIGEN 10 mg FILM-COATED TABLETS
Package Leaflet: Information for the User
Donepezil TecniGen 10 mg film-coated tablets EFG
Donepezil hydrochloride
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you:
Contents of the pack and other information
Donepezil TecniGen (donepezil hydrochloride) belongs to a group of medicines called acetylcholinesterase inhibitors. Donepezil increases the levels of a substance (acetylcholine) in the brain involved in memory function, making the breakdown of acetylcholine slower.
It is used to treat the symptoms of dementia in people diagnosed with mild to moderately severe Alzheimer's disease. The symptoms include increased memory loss, confusion, and changes in behavior. As a result, patients with Alzheimer's disease have increasing difficulty performing their normal daily activities.
It is a medicine for use only in adult patients.
Do not take Donepezil TecniGen
Warnings and precautions
Consult your doctor or pharmacist before starting to take Donepezil TecniGen.
Tell your doctor if you have or have had:
Also, tell your doctor if you are pregnant or think you may be pregnant.
Interaction of Donepezil TecniGen with other medicines
Tell your doctor or pharmacist if you are taking, have recently taken, or might take other medicines. This includes medicines that your doctor has not prescribed but that you may have obtained yourself from a pharmacy. It also applies to medicines that you may need to take in the future while you continue to take Donepezil TecniGen. These medicines may weaken or enhance the effects of Donepezil TecniGen.
In particular, it is important to tell your doctor or pharmacist if you are taking any of the following types of medicines:
If you are going to have surgery with general anesthesia, you must inform your doctor and anesthesiologist that you are taking Donepezil TecniGen, as this medicine may affect the amount of anesthetic needed.
Tell your doctor if you have any kidney or liver disease. Patients with severe liver disease should not take Donepezil TecniGen. Donepezil TecniGen can be used in patients with kidney disease and mild to moderate liver disease.
Tell your doctor or pharmacist about the name of your caregiver. Your caregiver can help you take the medicine that your doctor has prescribed.
Donepezil TecniGen with food, drink, and alcohol
Food does not affect the absorption of Donepezil TecniGen.
Donepezil TecniGen should not be taken with alcohol, as alcohol may change 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 medicine.
Donepezil TecniGen should not be used during breastfeeding.
Donepezil TecniGen should not be used during pregnancy except in clearly necessary cases.
Consult your doctor or pharmacist before taking any medicine.
Driving and using machines
Your illness may affect your ability to drive or use machines, and you should not perform these activities unless your doctor tells you it is safe to do so. Donepezil may cause dizziness and somnolence, mainly at the start of treatment or when increasing the dose. If you experience these effects, do not drive or use machines.
Donepezil TecniGen contains lactose
If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medicine.
Follow exactly the administration instructions of this medicine indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
How much Donepezil TecniGen should you take?
Normally, you will start taking 5 mg (1 white tablet) each night. After a month, your doctor may tell you to take 10 mg (1 yellow tablet) each night.
Swallow the tablet with water or another drink before going to bed at night. If you have abnormal dreams, nightmares, or difficulty sleeping (see section 4), your doctor may recommend that you take donepezil in the morning. The dose may change depending on the duration of treatment or your doctor's recommendation. The maximum recommended dose is 10 mg each night.
Always follow the recommendations of your doctor or pharmacist on how and when to take your medicine. Do not change the dose yourself without your doctor's advice.
How long should you take Donepezil TecniGen?
Your doctor or pharmacist will tell you how long you should take your tablets. You will need to visit your doctor regularly to review your treatment and analyze your symptoms.
If you stop taking Donepezil TecniGen
Do not stop taking the tablets unless your doctor tells you to do so. When treatment with Donepezil TecniGen is interrupted, the benefits of your treatment disappear gradually.
If you take more Donepezil TecniGen than you should
Do not take more than one tablet per day. In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone: 91 562 04 20, indicating the medicine and the amount ingested. Always carry the tablets and packaging with you so that the doctor knows what you are taking.
If you take more Donepezil TecniGen than you should, symptoms such as nausea, salivation, sweating, slow heart rate, low blood pressure (dizziness when standing up), breathing problems, loss of consciousness, epileptic seizures, or convulsions may occur.
If you forget to take Donepezil TecniGen
If you forget to take a dose, take only one dose the next day at the usual time. Do not take a double dose to make up for forgotten doses.
If you forget to take the medicine for more than a week, before taking the medicine again, consult your doctor.
If you have any other questions about the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The following side effects have been reported in people taking Donepezil TecniGen. Tell your doctor if you have any of these side effects while taking Donepezil TecniGen.
Serious side effects
You should tell your doctor immediately if you notice any of these serious side effects. You may need urgent medical treatment.
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)
Frequency not known
Frequency not known (cannot be estimated from the available data)
Reporting of side effects
If you experience any side effects, talk to your doctor or pharmacist, even if it is possible side effects that are not listed in this leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use Medicines: http://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
No special storage conditions are required.
Do not use this medicine after the expiry date stated on the packaging. The expiry date is the last day of the month indicated.
Medicines should not be disposed of via wastewater or household waste. Place the packaging and any unused medicine in the SIGRE collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and any unused medicine. This will help protect the environment.
Composition of Donepezil TecniGen
The active substance is donepezil hydrochloride.
Each tablet contains 10 mg of donepezil hydrochloride (equivalent to 9.12 mg of donepezil).
The other ingredients are: Core:Lactose monohydrate, Microcrystalline cellulose, Corn starch, Hydroxypropylcellulose, Magnesium stearate. Coating:Hypromellose, Titanium dioxide, Macrogol 400, Talc, and Yellow iron oxide.
Appearance of the product and pack size
Yellow, round, convex, film-coated tablets.
Available in blister packs in packs of 28 or 56 film-coated tablets.
Not all pack sizes may be marketed.
Other presentations:
Donepezil TecniGen 5 mg film-coated tablets EFG. Packs of 28 tablets.
Marketing authorization holder and manufacturer:
Marketing authorization holder:
Tecnimede España Industria Farmacéutica, S.A.
Avda. de Bruselas, 13, 3º D.
28108 Alcobendas (Madrid) SPAIN
Manufacturer:
Atlantic Pharma – Produções Farmacêuticas SA
Rua da Tapada Grande, 2, Abrunheira, 2710 – 089 Sintra
Portugal
Date of last revision of this leaflet: March 2023
Detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/
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