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Donepezil Hydrochloride 5mg Orodispersible Tablets

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Document: leaflet MAH GENERIC_PL 15773-0785 change

Package leaflet: Information for the user

Donepezil hydrochloride 5 mg orodispersible tablets Donepezil hydrochloride 10 mg orodispersible tablets

Donepezil hydrochloride

Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.

-    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 only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.

-    If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.

What is in this leaflet

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

2.    What you need to know before you take Donepezil hydrochloride

3.    How to take Donepezil hydrochloride

4.    Possible side effects

5.    How to store Donepezil hydrochloride

6.    Contents of the pack and other information

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

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 breakdown of acetylcholine.

Donepezil hydrochloride 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.

Donepezil hydrochloride is for use in adult patients only.

2.    What you need to know before you take Donepezil hydrochloride Do not take Donepezil hydrochloride

- if you are allergic to donepezil hydrochloride, to piperidine derivatives or any of the other ingredients of this medicine (listed in section 6).

Warnings and precautions

Talk to your doctor or pharmacist before taking Donepezil hydrochloride

•    if you have or have    had stomach or duodenal ulcers

•    if you have or have    had seizures (fits) or convulsions

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

•    if you have or have    had asthma or other long term lung disease

•    if you have or have    had liver problems or hepatitis

•    if you have or have    had difficulties passing urine or mild kidney disease

•    if you are going to    have an operation or if you need to have an anaesthetic before surgery.

Donepezil may exaggerate muscle relaxation during anaesthesia.

•    if you take anti-inflammatory medicines

If you are going to if you have difficulty passing urinehave an operation that requires you to have a general anaesthetic, you should tell your doctor and the anaesthetist that you are taking Donepezil hydrochloride. This is because your medicine may affect the amount of anaesthetic needed.

Donepezil hydrochloride can be used in patients with kidney diseaseif you have kidney or liver disease. Patients with severe liver disease should not take Donepezil hydrochloride.

Other medicines and Donepezil hydrochloride

Tell your doctor or pharmacist if you are taking/using, have recently taken/used or might take/use any other medicines. This includes medicines that your doctor has not prescribed for you but which you have bought yourself from a pharmacy. It also applies to medicines you may take sometime in the future if you continue to take Donepezil hydrochloride. This is because these medicines may weaken or strengthen the effects of Donepezil hydrochloride.

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 anti-inflammatory (NSAID) drugs such as ibuprofen, or diclofenac sodium

•    anticholinergics medicines, e.g. tolterodine

•    antibiotics e.g. erythromycin, rifampicin

•    anti-fungal medicine e.g. ketoconazole or itraconazole

•    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

Tell your doctor or pharmacist the name of your caregiver. Your caregiver will help you to take your medicine as prescribed.

Donepezil hydrochloride with food and alcohol

Food has no influence on the absorption of donepezil hydrochloride.

Donepezil hydrochloride should not be taken with alcohol because alcohol may change its effect. Pregnancy and breast-feeding

Donepezil hydrochloride should not be used during pregnancy or breast-feeding.

If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this 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.

3. How to take Donepezil hydrochloride

Always take this medicine exactly as your doctor has told you. Check with your doctor or pharmacist if you are not sure. You and your caregivers should be aware of the doctor’s instructions.

The recommended starting dose is 5 mg once daily. When Donepezil hydrochloride treatment of 5 mg/day has continued for one month, the dose can be increased by your doctor to 10 mg per day. The maximum recommended dose is 10 mg per day.

Kidney problems: No dosage adjustment needed.

Liver problems:

•    mild to moderate: Your dose is adjusted by your doctor.

•    severe: No data available, therefore Donepezil hydrochloride should not be used.

You should take Donepezil hydrochloride just before going to sleep. The tablet should be placed on the tongue and allowed to disintegrate before swallowing with or without water, according to your preference.

Use in children and adolescents

Donepezil hydrochloride is not recommended for use in children and adolescents.

For how long should you take Donepezil hydrochloride?

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

Overdosage with donepezil hydrochloride can result in cholinergic crisis (acetylcholine effect is too much) characterized by severe nausea, vomiting, salivation, sweating, slow heartbeat, low blood pressure, respiratory depression, collapse and convulsions. Increasing muscle weakness is a possibility and may result in death if respiratory muscles are involved.

If you have taken too many tablets, or another adult or a child has accidentally swallowed Donepezil hydrochloride, immediately contact a doctor, hospital or the Poison Information Centre. 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

Do not take a double dose to make up for a forgotten tablet. Take your normal dose on 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.

If you stop taking Donepezil hydrochloride

When Donepezil hydrochloride treatment is stopped, the beneficial effects of the treatment gradually disappear.

Do not stop taking Donepezil hydrochloride without first discussing it with your doctor.

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

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.

Serious side effects

You must tell your doctor immediately if you notice these serious side effects mentioned. You may

need urgent medical treatment.

Uncommon: may affect up to 1 in 100 people

•    Stomach or duodenal ulcers. The symptoms of ulcers are stomach pain and discomfort (indigestion) felt between the navel and the breast bone.

•    bleeding in the stomach or intestines. This may cause you to pass black tar like stools or visible blood from the rectum.

•    seizures (fits) or convulsions

Rare: may affect up to 1 in 1,000 people

•    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

Very rare: may affect up to 1 in 10,000 people

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

•    Muscle weakness, tenderness or pain and particularly, if at the same time, you feel unwell, have a high temperature or have dark urine. They may be caused by an abnormal muscle breakdown which can be life threatening and lead to kidney problems (a condition called rhabdomyolysis)

Other side effects

Tell your doctor if you have any of these effects while you are taking Donepezil hydrochloride

Very common: may affect more than 1 in 10 people

   diarrhoea

•    feeling or beeing sick

•    headache

Common: may affect up to 1 in 10 people

•    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

•    vomiting

•    stomach feeling uncomfortable

•    rash

•    itching

•    passing urine uncontrollably

•    pain

•    accidents (patients may be more prone to falls and accidental injury)

Uncommon: may affect up to 1 in 100 people

•    slow heart beat,

•    minor increase in serum concentration of muscle creatine kinase Rare: may affect up to 1 in 1,000 people

•    extrapyramidal symptoms (e.g. muscle stiffness, shaking or uncontrollable movements especially of the face and tongue but also of the limbs),

•    cardiac disorders (sinuatrial block or atrioventricular block)

Reporting of side effects

If you get 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 via the Yellow Card Scheme at: www.mhm.gov.uk/vellowcaid.

By reporting side effects you can help provide more information on the safety of this medicine.

5.    How to store Donepezil hydrochloride

Keep this medicine out of the sight and reach of children.

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

Store in the original package in order to protect from light and moisture.

Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.

6.    Contents of the pack and other information

What Donepezil hydrochloride contains

-    The active substance is donepezil hydrochloride.

Each film-coated tablet contains 5 mg or 10 mg donepezil hydrochloride

-    The other ingredients are

Mannitol (E 421), micocrystalline cellulose, disodium phosphate dihydrate, sodium stearyl fumarate, flavour peppermint (containing menthol, thymol, methyl-tert-butylether, maltodextrin and modified starch), flavour menthol (containing menthol and gum arabic) and saccharin sodium.

Only in 10 mg tablets pigment blend yellow containing iron oxide (E 172) and microcrystalline cellulose.

What Donepezil hydrochloride looks like and contents of the pack

5 mg: White, round, biconvex tablet, embossed with ‘D’ on one side.

10 mg: Yellow, round, biconvex tablet, embossed with ‘D’ on one side.

Packs with 7, 10, 14, 28, 30, 3x30, 50, 56, 60, 98, 100 and 120 orodispersible tablets

Not all pack sizes may be marketed.

Marketing Authorisation Holder and Manufacturer

Marketing Authorisation Holder: Ratiopharm GmbH, Graf-Arco-Strasse 3, D-89079 Ulm, Germany

Manufacturer: HBM Pharma s.r.o., Sklabinska 30, 036 80 Martin, Slovak Republic

OR*

Merckle GmbH, Ludwig-Merckle-Strasse 3, 89143 Blaubeuren, Germany OR*

Teva Pharmaceutical Works Private Ltd.

Pallagi Ut 13 4042 Debrecen Hungary

This leaflet was last revised in April 2016

PL 15773/0785-6

* Only the paragraph containing the details of the current batch release site will be included in the printed version of the PIL

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