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Donepezil Hydrochloride 5mg Orodispersible Tablets

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PACKAGE LEAFLET: INFORMATION FOR THE USER

Donepezil hydrochloride 5 mg Orodispersible tablet Donepezil hydrochloride 10 mg Orodispersible tablet

(Donepezil Hydrochloride)

Read all of this leaflet carefully before you start using 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 gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.

In this leaflet:

1.    What Donepezil hydrochloride is and what it is used for

2.    Before you take Donepezil hydrochloride

3.    How to take Donepezil hydrochloride

4.    Possible side effects

5.    How to store Donepezil hydrochloride

6.    Further information

1. WHAT DONEPEZIL HYDROCHLORIDE IS AND WHAT IT IS USED FOR

Donepezil hydrochloride (donepezil hydrochloride) belongs to a group of medicines called acetylcholinesterase inhibitors.

It is used to treat the symptoms of dementia (disorder of rational behaviour) in people diagnosed as having mild to moderately severe Alzheimer's disease (a chronic mental disease). It is for use only in adult patients.

2. BEFORE YOU TAKE DONEPEZIL HYDROCHLORIDE Do not take Donepezil hydrochloride if:

• you a re a llergic (hypersensitive) t o don epezil hy drochloride, or to p iperidine derivatives, or a ny other ingredients of Donepezil hydrochloride listed in section 6.

Take special care with Donepezil hydrochloride

Tell your doctor or pharmacist if:

•    you have ever had stomach or duodenal ulcers

•    you have ever had a seizure (fit) or convulsion

•    you have a heart condition (irregular or very slow heart beat)

•    you have asthma (dyspnoea) or other long term lung disease

•    you have ever had any liver problems or hepatitis (inflammation of the liver)

•    you have difficulty passing urine or mild kidney disease

Taking other medicines

Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription. Always tell your doctor or pharmacist if you are using or receiving any of the following medicines in addition to Donepezil hydrochloride:

•    other Alzheimer’s disease medicines, e.g. galantamine

•    pain killers or treatment for arthritis e.g. aspirin, non-steroidal anti-inflammatory (N SAID) drugs such as ibuprofen, or diclofenac sodium

•    anticholinergics medicines, e.g. tolterodine

•    antibiotics e.g. erythromycin, rifampicin

•    anti-fungal medicines e.g. ketoconazole

•    muscle relaxants e.g. diazepam, succinylcholine

•    anti-depressants e.g. fluoxetine

•    anticonvulsants (medicines used in prevention of the occurrence of several types of seizures) e.g. phenytoin, carbamazepine

•    medication for a heart condition e.g. quinidine, beta-blockers (propanolol and atenolol)

•    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 (narcosis) you should t ell y our doc tor a nd t he a naesthetist t hat y ou a re t aking Donepezil hy drochloride.This i s because your medicine may affect the amount of anaesthetic needed.

Donepezil hydrochloride 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 Donepezil hydrochloride.

Taking Donepezil hydrochloride with food and drink

Donepezil hydrochloride may be taken with a glass of water once the tablet has dissolved on the tongue. Food does not have any effect on this medication. Alcohol consumption should be restricted when taking Donepezil hydrochloride, as alcohol may reduce the levels of donepezil.

Pregnancy and breast-feeding

You should not use donepezil hydrochloride if you are pregnant or are breast feeding.

Ask your doctor or your pharmacist for advice before taking any medicine.

Driving and using machines

Do not drive because 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.

Do not use any tools or machines because your medicine can cause fatigue, dizziness and muscle cramp and if affected you must not drive or operate machinery.

Important information about some of the ingredients of Donepezil hydrochloride

Contains source of phenylalanine. May be harmful for people with phenylketonuria.

This product contains lactose. If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this product.

3. HOW TO TAKE DONEPEZIL HYDROCHLORIDE

Always take Donepezil hydrochloride exactly as your doctor has told you. You should check with your doctor or your pharmacist if you are not sure.

The usual dose is 5 mg every night. After one month, your doctor may tell you to take 10 mg every night. The maximum recommended dose is 10 mg each night.

Take your Donepezil hydrochloride by mouth at night before you go to bed. The tablet should be placed on the tongue and allowed to dissolve before swallowing with or without water according to your preference.

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 will recommend. You should 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. 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 take more Donepezil hydrochloride than you should

Do not take more than one tablet each day. If you do, you may experience nausea, vomiting, drooling, sweating, slow heart rate, low blood pressure (light-headedness or dizziness when standing), difficulty in breathing, collapse and convulsion. Call your doctor immediately or contact the local hospital. Always take the tablets and the carton with you to the hospital so that the doctor knows what has been taken.

If you forget to take Donepezil hydrochloride

If you forget to take a tablet, just take one tablet the following day at the usual time. If you forget to take your medicine for more than one week, call your doctor before taking any more medicine. Do not take a double dose to make up for a forgotten tablet.

If you stop taking Donepezil hydrochloride

Do not stop taking the tablets unless told to do so by your doctor.

If you have any further question on the use of this product, ask your doctor or your pharmacist.

4. POSSIBLE SIDE EFFECTS

Like all medicines, Donepezil hydrochloride can have side effects, although not everybody gets them. In most cases these go away without having to stop treatment. Tell your doctor if you have any of these effects and if they are too uncomfortable for you.

Patients taking Donepezil hydrochloride have reported following side effects. Tell your doctor if you have any of these effects while you are taking Donepezil hydrochloride.

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 (probably affecting fewer than 1 in 1,000).

•    stomach or duodenal ulcers. The symptoms of ulcers are stomach pain and discomfort (indigestion) felt between the navel and the breast bone (probably affecting fewer than 1 in 100).

•    bleeding in the stomach or intestines. This may cause you to pass black tar like stools or visible blood from the rectum (probably affecting fewer than 1 in 100).

•    seizures (fits) or convulsions (probably affecting fewer than 1 in 100).

•    fever with muscle stiffness, sweating or a lowered level of consciousness (a disorder called “Neuroleptic Malignant Syndrome”)

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)

   common cold

abdominal disturbances rash


•    loss of appetite    •

•    hallucinations (seeing or hearing things that • are not really there

•    agitation

itching

muscle cramp urinary incontinence fatigue pain


•    aggressive behaviour

•    fainting

•    dizziness

•    insomnia (difficulty in sleeping)

•    accidents

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 or uncontrollable movement especially of the face and tongue but also of the limbs

If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or your pharmacist.

5. HOW TO STORE DONEPEZIL HYDROCHLORIDE

Keep out of the reach and sight of children.

Do not use Donepezil hydrochloride after the expiry date which is stated on the blister and the carton. The expiry date refers to the last day of that month.

This medicinal product does not require any special storage conditions

Medicines should not be disposed of via wastewater or household waste. Ask yor pharmacist how to dispose of medicines no longer required. These measures will help to protect the enviroment.

6. FURTHER INFORMATION What Donepezil hydrochloride

The active substance in Donepezil hydrochloride is donepezil hydrochloride.

5mg: Each tablet contains 5 mg of donepezil hydrochloride.

10mg: Each tablet contains 10 mg of donepezil hydrochloride.

The other ingredients are: polacrilin potassium, microcrystalline cellulose, lactose monohydrate (spray dried), monosodium citrate anhydrous, aspartame (E951), croscarmellose sodium, silica colloidal anhydrous, magnesium stearate, hydrochloric acid for pH adjustments

What Donepezil hydrochloride looks like and contents of the pack

White to off-white round, flat tablets, with bevelled edges, containing 5 mg of Donepezil HCl, embossed with ‘5’ on one side and plain on the other

White to off-white round, flat tablets, with bevelled edges, containing 10 mg of Donepezil HCl, embossed with ‘10’ on one side and plain on the other

Packs:

PVC /Aclar/Aluminium and Aluminium/Aluminium blisters of 7, 10, 14 tablets Pack sizes: 7, 28, 30, 50, 56, 60, 98, 120 orodispersible tablets Not all pack sizes may be marketed.

Marketing Authorisation Holder and Manufacturer:

Marketing Authorisation Holder:

Glenmark Generics (Europe) Limited, The Old Sawmill, Hatfield Park, Hatfield, Hertfordshire, AL9 5PG, United Kingdom

Manufacturer:

Genepharm Group, 18 Km Marathon Avenue, 15351 Greece

This medicinal product is authorised in the member states of the EEA under the following names:

Bulgaria    Cognezil ODT 5 mg orodispersible tablet / Cognezil ODT 5 mg

orodispersible tablet

Czech Republic Alzil Orotab 5 mg / Alzil Orotab 10 mg

Hungary    Cognezil 5 mg szajban diszpergalodo tabletta / Cognezil 10 mg szajban

diszpergalodo tabletta Poland    Cognezil ODT

Romania    Cognezil OD 5 mg comprimate orodispersabile / Cognezil OD 10 mg

comprimate orodispersabile

Slovakia    Cognezil Orotab 5 mg / Cognezil Orotab 10 mg

This leaflet was last approved in 12/2012