Donepezil Hydrochloride
Donecept belongs to a group of medications called acetylcholinesterase inhibitors. Donepezil increases the concentration of a substance (acetylcholine) involved in memory function by slowing down the breakdown of acetylcholine.
This medication is used to treat the symptoms of dementia in patients diagnosed with mild and moderate Alzheimer's disease. The symptoms of the disease may include increasing memory loss, feeling disoriented, and changes in behavior. As a result, people with Alzheimer's disease may find it increasingly difficult to perform their daily tasks.
The medication is intended for use only in adult patients.
You should also inform your doctor if you are pregnant or think you may be pregnant.
Donecept is not recommended for use in children and adolescents (under 18 years of age).
Tell your doctor or pharmacist about all medications you are taking, have recently taken, or plan to take. This includes medications that have not been prescribed by a doctor and that you have bought yourself in a pharmacy. It also includes medications that you will take for a certain period in the future with Donecept. This is important because these medications may weaken or enhance the effect of Donecept.
It is especially important to tell your doctor if you are taking any of the following types of medications:
A patient who is to undergo surgery requiring general anesthesia should inform the doctor that they are taking Donecept. Donecept may affect the amount of anesthetic needed.
Donecept can be used in patients with kidney and mild to moderate liver impairment. You should inform your doctor about kidney or liver diseases. Patients with severe liver impairment should not take Donecept.
You should indicate to your doctor or pharmacist who is the patient's caregiver. The caregiver will help the patient take their medications as prescribed.
Food does not affect the action of Donecept.
During treatment with Donecept, you should not consume alcohol, as alcohol may alter the effect of the medication.
If you are pregnant or breastfeeding, think you may be pregnant, or plan to have a child, ask your doctor or pharmacist for advice before taking any medication.
Donecept should not be used during breastfeeding.
Alzheimer's disease may impair your ability to drive or operate machinery.
You should not perform these activities unless your doctor considers it safe. The medication may cause drowsiness, dizziness, and muscle cramps. If these symptoms occur, you should not drive or operate machinery.
If you have been told you have an intolerance to some sugars, contact your doctor before taking this medication.
Always take this medication exactly as your doctor or pharmacist has told you. If you are unsure, ask your doctor or pharmacist. The recommended starting dose is 5 mg (one white tablet) taken once daily in the evening before bedtime. After one month, your doctor may increase the dose to 10 mg (one yellow tablet) taken once daily in the evening before bedtime.
If you experience unusual dreams, nightmares, or difficulty sleeping (see section 4), your doctor may recommend taking Donecept in the morning.
The dose of the tablet you take may change depending on the duration of treatment and your doctor's recommendations. The maximum recommended daily dose is 10 mg taken in the evening.
Always follow the instructions of your doctor or pharmacist regarding the method and time of taking the medication. Do not change the dose yourself without consulting your doctor.
Take Donecept orally with a glass of water in the evening immediately before bedtime.
Donepezil is not recommended for use in children and adolescents (under 18 years of age).
In case of overdose, contact your doctor or hospital immediately. Bring the package leaflet and any remaining tablets with you.
Symptoms of overdose may include nausea, vomiting, salivation, sweating, slow heartbeat, low blood pressure (dizziness when standing), difficulty breathing, loss of consciousness, and seizures.
If you miss a dose, take the next dose at the scheduled time. Do not take a double dose to make up for the missed dose.
If treatment has been interrupted for more than one week, consult your doctor before taking the next dose.
Do not stop taking the tablets unless your doctor tells you to. If you stop treatment, the benefits of donepezil will gradually fade.
If you have any further questions about the use of this medication, ask your doctor or pharmacist.
Your doctor or pharmacist will inform you how long to continue taking the tablets.
Regular check-ups with your doctor will be necessary to assess your treatment and symptoms.
If you have any further questions about the use of this medication, ask your doctor or pharmacist.
Like all medications, Donecept can cause side effects, although not everybody gets them.
The following side effects have been reported in patients taking Donecept.
If any of the following side effects occur while taking Donecept, consult your doctor.
If you experience any of the following severe side effects, contact your doctor immediately. You may need urgent medical attention.
Very Common: may affect more than 1 in 10 patients:
Common: may affect up to 1 in 10 patients:
Uncommon: may affect up to 1 in 100 patients:
Rare: may affect up to 1 in 1,000 patients:
Unknown: frequency cannot be estimated from the available data
If you experience any side effects, including any not listed in this leaflet, please tell your doctor, pharmacist, or nurse. You can also report side effects directly to the Department of Drug Safety Monitoring of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products, Al. Jerozolimskie 181C, 02-222 Warsaw, tel.: +48 22 49 21 301, fax: +48 22 49 21 309, website: https://smz.ezdrowie.gov.pl. You can also report side effects to the marketing authorization holder. By reporting side effects, you can help provide more information on the safety of this medication.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiry date stated on the blister pack and carton after EXP. The expiry date refers to the last day of the month.
There are no special storage precautions.
Medications should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medications no longer required. This will help protect the environment.
Donecept, 5 mg, film-coated tablet, white, round, and biconvex with the inscription "DZ5" on one side.
Donecept, 10 mg, film-coated tablet, pale yellow, round, and biconvex with the inscription "DZ10" on one side.
Pack sizes: Blister: 28, 30, 56, and 60 film-coated tablets.
Actavis Group PTC ehf.
Dalshraun 1, 220 Hafnarfjörður, Iceland
Actavis Ltd.
BLB 016 Bulebel Industrial Estate
Zejtun ZTN 3000, Malta
Actavis Group PTC ehf.
Dalshraun 1, IS-220 Hafnarfjörður, Iceland
Balkanpharma-Dupnitsa AD
3 Samokovska Shosse Str.
2600, Dupnitsa, Bulgaria
Teva Pharmaceuticals Polska Sp. z o.o., ul. Emilii Plater 53, 00-113 Warsaw, tel. (22) 345 93 00.
Estonia
Donepezil Actavis
Austria
Donepezil Actavis 5 mg Filmtabletten
Donepezil Actavis 10 mg Filmtabletten
Czech Republic
Donepezil Actavis
Iceland
Donepezil Actavis
Lithuania
Donepezil Actavis 5 mg plėvele dengtos tabletės
Donepezil Actavis 10 mg plėvele dengtos tabletės
Malta
Donecept
Norway
Donepezil Actavis
Poland
Donecept
Romania
Donecept 5 mg, comprimate filmate
Donecept 10 mg, comprimate filmate
Sweden
Donepezil Actavis
Date of Last Revision of the Leaflet:January 2024
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