Kraj: Irlandia
Język: angielski
Źródło: HPRA (Health Products Regulatory Authority)
DONEPEZIL HYDROCHLORIDE
Clear Pharmacy
N06DA02
DONEPEZIL HYDROCHLORIDE
10 Milligram
Film Coated Tablet
Product subject to prescription which may not be renewed (A)
Anticholinesterases
Authorised
2011-06-23
PACKAGE LEAFLET: INFORMATION FOR THE USER ARICEPT® 5 MG FILM COATED TABLETS ARICEPT® 10 MG FILM COATED 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 of the side effects talk to your doctor or pharmacist. This includes any side possible effects not listed in this leaflet. See section 4. WHAT IS IN THIS LEAFLET 1. WHAT ARICEPT IS AND WHAT IT IS USED FOR 2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE ARICEPT 3. HOW TO TAKE ARICEPT 4. POSSIBLE SIDE EFFECTS 5. HOW TO STORE ARICEPT 6. CONTENTS OF THE PACK AND OTHER INFORMATION 1. WHAT ARICEPT IS AND WHAT IT IS USED FOR ARICEPT contains the active substance donepezil hydrochloride. ARICEPT (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 is for use in adult patients only. 2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE ARICEPT DO NOT TAKE ARICEPT • if you are allergic to donepezil hydrochloride, or 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 ARICEPT if you have or have had: • stomach or duodenal ulcers • seizures (fits) or Przeczytaj cały dokument
SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT Aricept 10mg Film-coated Tablets 2 QUALITATIVE AND QUANTITATIVE COMPOSITION 10 mg donepezil hydrochloride tablets each containing 9.12 mg of donepezil free base. Excipient: lactose monohydrate 174.33 mg per tablet. For full list of excipients, see section 6.1. 3 PHARMACEUTICAL FORM Film-coated Tablet _Product imported from the Czech Republic:_ Yellow round, biconvex tablets embossed ‘ARICEPT’ on one side and ‘10’ on the other side. 4 CLINICAL PARTICULARS As per PA0822/002/002 5 PHARMACOLOGICAL PROPERTIES As per PA0822/002/002 6 PHARMACEUTICAL PARTICULARS 6.1 LIST OF EXCIPIENTS Lactose monohydrate Maize starch Microcrystalline cellulose Hyprolose Magnesium stearate _film coating_ Talc Macrogol 8000 Hypromellose Titanium dioxide (E171) Yellow iron oxide (E172) 6.2 INCOMPATIBILITIES Not applicable 6.3 SHELF LIFE The shelf-life expiry date of this product shall be the date shown on the container and outer packaging of the product on the market in the country of origin. H E A L T H P R O D U C T S R E G U L A T O R Y A U T H O R I T Y ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ ___ _D_ _a_ _t_ _e_ _ _ _P_ _r_ _i_ _n_ _t_ _e_ _d_ _ _ _1_ _1_ _/_ _0_ _1_ _/_ _2_ _0_ _1_ _7_ _C_ _R_ _N_ _ _ _2_ _1_ _8_ _7_ _2_ _5_ _5_ _p_ _a_ _g_ _e_ _ _ _n_ _u_ _m_ _b_ _e_ _r_ _:_ _ _ _1_ 6.4 SPECIAL PRECAUTIONS FOR STORAGE Do not store above 30°C. 6.5 NATURE AND CONTENTS OF CONTAINER Blisters in cardboard cartons of 28 tablets. 6.6 SPECIAL PRECAUTIONS FOR DISPOSAL OF A USED MEDICINAL PRODUCT OR WASTE MATERIALS DERIVED FROM SUCH MEDICINAL PRODUCT Przeczytaj cały dokument