Aricept 10mg Tablets
PATIENT INFORMATION LEAFLET
Revision Date: 27 03 2015
ARICEPT® 5MG TABLETS Leaflet reference: ARIC 5,10R/UT
ARICEPT® 10MG TABLETS
(Donepezil hydrochloride)
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This product is known by either of the above names, but will be referred to as Aricept® Tablets throughout this leaflet.
You and your caregiver should read all of this leaflet carefully before you start taking this medicine.
• Keep this leaflet. You may need to read it again.
• If you have any further questions, ask your doctor or pharmacist.
• This medicine has been prescribed for you. Do not pass it on to others. It may harm them, even if their symptoms are the same as yours.
• If any of the side effects get serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.
In this leaflet:
1. What Aricept® Tablets are and what they are used for
2. Before you take Aricept® Tablets
3. How to take Aricept® Tablets
4. Possible side effects
5. How to store Aricept® Tablets
6. Further information
1. WHAT ARICEPT® TABLETS ARE AND WHAT THEY ARE USED FOR
Aricept® Tablets (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 by slowing down the break down of acetylcholine.
It is used to treat the symptoms of dementia in people diagnosed as having mild and moderately severe Alzheimer's disease.
The symptoms include increasing memory loss, confusion and behavioural changes. As a result, sufferers of Alzheimer's disease find it more and more difficult to carry out their normal daily activities.
Aricept® Tablets are for use in adult patients only.
2. BEFORE YOU TAKE ARICEPT® TABLETS
Do NOT take Aricept® Tablets
• if you are allergic (hypersensitive) to donepezil hydrochloride or to piperidine derivatives, or any of the other ingredients of Aricept® Tablets listed in section 6
Take special care with Aricept® Tablets
Tell your doctor or pharmacist before starting to take Aricept® Tablets if you have or have had:
• stomach or duodenal ulcers
• seizures (fits) or convulsions
• a heart condition (irregular or very slow heartbeat)
• asthma or other long term lung disease
• liver problems or hepatitis
• difficulty passing urine or mild kidney disease
Also tell your doctor if you are pregnant or think you might be pregnant.
Taking other medicines
Please tell your doctor or pharmacist if you are taking, or have recently taken, any other medicine. This includes medicines that your doctor has not prescribed for you but which you have bought yourself from a chemist/pharmacist. It also applies to medicines you may take sometime in the future if you continue to take Aricept® T ablets. This is because these medicines may weaken or strengthen the effects of Aricept®
Tablets.
Especially tell your doctor if you are taking any of the following types of medicines:
• other Alzheimer's disease medicines, e.g. galantamine
• pain killers or treatment for arthritis e.g. aspirin, non-steroidal antiinflammatory (NSAID) drugs such as ibuprofen, or diclofenac sodium
• anticholinergics medicines, e.g. tolterodine
• antibiotics e.g. erythromycin, rifampicin
• anti-fungal medicine e.g. ketoconazole
• anti-depressants e.g. fluoxetine
• anticonvulsants e.g. phenytoin, carbamazepine
• medication for a heart condition e.g. quinidine, beta-blockers (propanolol and atenolol)
• muscle relaxants e.g. diazepam, succinylcholine
• general anaesthetic
• medicines obtained without a prescription e.g. herbal remedies
If you are going to have an operation that requires you to have a general anaesthetic you should tell your doctor and the anaesthetist that you are taking Aricept® Tablets.
This is because your medicine may affect the amount of anaesthetic needed.
Aricept® Tablets can be used in patients with kidney disease or mild to moderate liver disease. Tell your doctor first if you have kidney or liver disease. Patients with severe liver disease should not take Aricept® Tablets.
Tell your doctor or pharmacist the name of your caregiver. Your caregiver will help you to take your medicine as it is prescribed.
Taking Aricept® Tablets with food and drink
Food will not influence the effect of Aricept® Tablets
Aricept® Tablets should not be taken with alcohol because alcohol may
change its effect.
Pregnancy and breast-feeding
Aricept® Tablets should not be used while breast-feeding.
If you are pregnant, or think you might be pregnant, ask your doctor for advice before taking any medicine.
Driving and using machines
Alzheimer's disease may impair your ability to drive or operate machinery and you must not perform these activities unless your doctor tells you that it is safe to do so.
Also, your medicine can cause tiredness, dizziness and muscle cramp. If you experience any of these effects you must not drive or operate machinery.
Important information about some of the ingredients of Aricept® Tablets
This product contains lactose. If you have been told by your doctor that you have intolerance to some sugars, you should contact your doctor before taking Aricept® Tablets.
3. HOW TO TAKE ARICEPT® TABLETS
How much Aricept® Tablets should you take?
Usually, you will start by taking 5mg (one white tablet) every night. After one month, your doctor may tell you to take 10mg (one yellow tablet) every night.
Swallow your Aricept® tablet with a drink of water before you go to bed at night.
The tablet strength you will take may change depending on the length of time you have been taking the medicine and on what your doctor recommends. The maximum recommended dose is 10mg each night. Always follow your doctor's, or pharmacist's advice about how and when to take your medicine.
Do not alter the dose yourself without your doctor's advice.
The following is a translation of the days of the week shown on the blister
For how long should you take Aricept® Tablets?
Your doctor or pharmacist will advise you on how long you should continue to take your tablets. You will need to see your doctor from time to time to review your treatment and assess your symptoms.
If you stop taking Aricept® Tablets
Do not stop taking the tablets unless told to do so by your doctor. If you stop taking Aricept® Tablets the benefits of your treatment will gradually fade away.
If you take more Aricept® Tablets than you should
DO NOT take more than one tablet each day. Call your doctor immediately if you take more than you should. If you cannot contact your doctor, contact the local hospital Accident and Emergency department at once. Always take the tablets and the carton with you to the hospital so that the doctor knows what has been taken.
Symptoms of overdosing include feeling and being sick, drooling, sweating, slow heart rate, low blood pressure (light-headedness or dizziness when standing), breathing problems, losing consciousness and seizures (fits) or convulsions.
If you forget to take Aricept® Tablets
If you forget to take a tablet, just take one tablet the following day at the usual time.
Do not take a double dose to make up for a forgotten tablet.
If you forget to take your medicine for more than one week, call your doctor before taking any more medicine
4. POSSIBLE SIDE EFFECTS
Like all medicines, Aricept® Tablets can cause side effects, although not everybody gets them.
The following side effects have been reported by people taking Aricept® Tablets.
Tell your doctor if you have any of these effects while you are taking Aricept® Tablets.
Serious side effects:
You must tell your doctor immediately if you notice these serious side effects mentioned. You may need urgent medical treatment.
• liver damage e.g. hepatitis. The symptoms of hepatitis are feeling or being sick, loss of appetite, feeling generally unwell, fever, itching, yellowing of the skin and eyes, and dark coloured urine (affects1 to 10 users in 10,000).
• stomach or duodenal ulcers. The symptoms of ulcers are stomach pain and discomfort (indigestion) felt between the navel and the breast bone (affects 1 to 10 users in 1,000).
• bleeding in the stomach or intestines.
This may cause you to pass black tar-like stools or visible blood from the rectum (affects 1 to 10 users in 1,000).
• seizures (fits) or convulsions (affects 1 to 10 users in 1,000).
• Fever with muscle stiffness, sweating or a lowered level of consciousness (a disorder called “Neuroleptic Malignant Syndrome”) (affects less than 1 user in 10,000)
Very common side effects (affects more than 1 user in 10):
• diarrhoea
• feeling or being sick
• headaches
Common side effects (affects 1 to 10 users in 100):
• muscle cramp
• tiredness
• difficulty in sleeping (insomnia)
• the common cold
• loss of appetite
• hallucinations (seeing or hearing things that are not really there)
• unusual dreams including nightmares
• agitation
• aggressive behaviour
• fainting
• dizziness
• stomach feeling uncomfortable
• rash
• itching
• passing urine uncontrollably
• pain
• accidents (patients may be more prone to falls and accidental injury) Uncommon side effects (affects 1 to 10 users in 1,000):
• slow heart beat
Rare side effects (affects 1 to 10 users in 10,000):
• stiffness, shaking or uncontrollable movement especially of the face and tongue but also of the limbs
Reporting of side effects
If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard. By reporting side effects, you can help provide more information on the safety of this medicine.
5. HOW TO STORE ARICEPT® TABLETS
• Do not store above 30°C.
• Keep out of the sight and reach of children.
• Do not use this medicine after the expiry date shown on the carton label or blister.
• If your doctor tells you to stop taking this medicine, return any unused tablets to your pharmacist for safe disposal. Only keep this medicine, if your doctor tells you to.
• If your tablets become discoloured or show any other signs of deterioration, consult your pharmacist who will tell you what to do.
6. FURTHER INFORMATION What do Aricept® Tablets contain?
Aricept® Tablets contain either 5mg or 10mg of the active ingredient donepezil (as hydrochloride).
Each tablet also contains lactose, maize starch, microcrystalline cellulose, hydroxypropyl cellulose, magnesium stearate, hypromellose, talc, polyethylene glycol, titanium dioxide (E171).
The 10mg tablet also contains yellow iron oxide (E172).
What do Aricept® Tablets look like?
The 5mg tablets are white, round, film-coated tablet and marked ‘ARICEPT' on one side, ‘5' on the reverse.
The 10mg tablets are yellow, round, film-coated tablet and marked ‘ARICEPT' on one side, ‘10' on the reverse.
Aricept® Tablets are available in calendar blister packs of 28 tablets.
Who manufactured your medicine
Manufactured by Pfizer PGM., Zone Industrielle, 29 Route des Industries, 37530 Poce-Sur-Cisse, France. Procured from within the EU and repackaged by Product Licence holder: Beachcourse Limited, 20 Alliance Court, Alliance Road, London W3 0RB.
Aricept® 5 mg Tablets PL 16378/0110 _
Aricept® 10 mg Tablets PL 16378/0111 |POM|
Revision Date: 27 03 2015 Leaflet reference: ARIC 5,10R/UT
Aricept is a registered trademark of Eisai Limited