


Ask a doctor about a prescription for DONEPEZIL PENSA 10 mg FILM-COATED TABLETS
Package Leaflet: Information for the User
Donepezil Pensa 10mg 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 belongs to a group of medicines called acetylcholinesterase inhibitors: it increases the levels in the brain of a substance related to memory (acetylcholine) by reducing the speed of breakdown of this substance.
It is used for the treatment of the symptoms of Alzheimer's disease of mild to moderate severity. The symptoms include increased memory loss, confusion, and behavioral changes.
Remember:You must tell your doctor who your caregivers are.
Do not takeDonepezil Pensa
Warnings and precautions
Consult your doctor or pharmacist before starting to take Donepezil Pensa.
Treatment with donepezil should only be initiated and supervised by a doctor with experience in the diagnosis and treatment of Alzheimer's disease.
Consult your doctor or pharmacist before starting to take Donepezil Pensa if you have or have had:
You must avoid taking Donepezil Ranbaxy with other acetylcholinesterase inhibitors and other agonists or antagonists of the cholinergic system.
The individual effect of donepezil cannot be predicted, therefore the effect of treatment should be regularly evaluated by the doctor.
Children:
Donepezil is not recommended for use in children.
Other medicines and Donepezil Pensa
Tell your doctor if you are using, have recently used, or might use any other medicines, including those obtained without a prescription.
In particular, it is important that you inform your doctor if you are taking any of the following types of medicines:
In case of surgical intervention with general anesthesia, you must inform your doctor that you are taking Donepezil Pensa, as this may affect the amount of anesthetic needed. Donepezil Pensa can be used in patients with mild to moderate renal or hepatic impairment. Inform your doctor if you have any kidney or liver problems. Patients with severe hepatic impairment should not take Donepezil Pensa.
Taking Donepezil Pensa with food, drink, and alcohol
Taking Donepezil Pensa with alcohol may alter the absorption of this medicine.
You should avoid drinking alcohol while being treated with donepezil, as it may reduce the effect of donepezil.
Pregnancy, breast-feeding, and fertility
If you are pregnant or breast-feeding, or think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Do not take donepezil if you are pregnant or think you may be pregnant.
Do not take donepezil if you are breast-feeding.
Driving and using machines
Your illness may affect your ability to drive or use machines, and you should not carry out these activities unless your doctor tells you it is safe to do so. Donepezil may cause dizziness, drowsiness, somnolence, and muscle cramps, mainly at the start of treatment or when increasing the dose. If you experience these effects, do not drive or use machines.
Donepezil Pensa contains lactose
Donepezil Pensa contains lactose. If your doctor has told you that you have an intolerance to some sugars, consult them before taking this medicine.
Follow exactly the administration instructions of this medicine given by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again. The usual dose is described below. You should take donepezil once a day orally with a glass of water in the evening, immediately before bedtime.
The dose you take may vary depending on how long you have been taking the medicine and what your doctor recommends. You will usually start by taking
5 mg each night. After a month, your doctor may tell you to take 10 mg each night. The maximum recommended dose is 10 mg each night.
If you have abnormal dreams, nightmares, or difficulty sleeping (see section 4), your doctor may recommend that you take Donepezil Pensa in the morning.
Both you and your caregivers should know the doctor's instructions.
If you have mild to moderate hepatic (liver) or renal (kidney) impairment, you can take Donepezil Pensa. Inform your doctor before starting treatment if you have liver or kidney problems. Patients with severe hepatic impairment should not take Donepezil Pensa.
Use in children:
Donepezil is not recommended for use in children.
If you take more Donepezil Pensa than you should
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.
Symptoms of overdose may include dizziness, drooling, sweating, decreased heart rate, low blood pressure (dizziness or fainting when standing up), breathing problems, loss of consciousness, and seizures
If you forget to take Donepezil Pensa
If you forget to take a dose, take the missed dose as soon as you remember, unless it is time for the next dose.
Do not take a double dose to make up for forgotten doses.
If you stop taking Donepezil Pensa
Do not stop taking Donepezil Pensa unless your doctor tells you to. If you stop taking Donepezil Pensa, the benefits of treatment will gradually disappear
If you have any further questions on the use of this product, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Very common side effects(≥1/10) are:Diarrhea, nausea, headache.
Common side effects(seen in at least 1 in 100 patients) are: dizziness, insomnia, fatigue, fainting, hallucinations, agitation, aggressive behavior, abnormal dreams and nightmares, fatigue, pain, loss of appetite, digestive disorders, such as diarrhea, nausea, and vomiting, incontinence, muscle cramps, skin rash, itching, colds, and accidents.
Uncommon side effects(≥1/1,000 to <1>
Rare side effects(≥1/10,000 to <1>
Frequency not known
Very rare and serious side effects
Consult your doctor immediately if you experience these serious side effects. You may need urgent medical treatment.
If you experience hallucinations, agitation, aggressive behavior, seizures, or brief episodes of fainting, you should consult your doctor, as you may need to lower the dose or stop treatment.
Serious side effects:
Consult your doctor immediately if you experience these serious side effects. You may need urgent medical treatment:
If you experience any side effect that is severe or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.
Reporting of side effects
If you experience any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly to the Spanish Medicines and Healthcare Products Agency (AEMPS) via their website: https://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.
Do not use Donepezil Pensa after the expiry date stated on the carton. The expiry date refers to the last day of the month shown.
No special storage conditions are required.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help protect the environment.
Composition of Donepezil Pensa 10mg
The film coating contains: talc (E-553b), macrogol, hypromellose, titanium dioxide (E-171), yellow iron oxide (E-172).
Appearance and packaging of the product
Donepezil Pensa 10 mg are film-coated tablets, capsule-shaped, scored on both sides, yellow in color, and with the text "RC&26" on both sides of the score line on one side. The 10 mg tablets are available in pack sizes of 28 tablets and a clinical pack of 50 tablets.
Donepezil Pensa 5 mg is also available in pack sizes of 28 tablets and a clinical pack of 50 tablets.
Not all pack sizes may be marketed.
Marketing authorization holder
Towa Pharmaceutical, S.A.
C/ de Sant Martí, 75-97
08107 Martorelles (Barcelona)
Spain
Manufacturer
Sun Pharmaceutical Industries Europe B.V.,
Polarisavenue 87,
2132JH Hoofddorp,
Netherlands
Date of last revision of this leaflet:September 2022
Detailed 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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