Страна: Ірландія
мова: англійська
Джерело: HPRA (Health Products Regulatory Authority)
Etoricoxib
IMED Healthcare Ltd.
M01AH05
Etoricoxib
90 milligram(s)
Film-coated tablet
Product subject to prescription which may be renewed (B)
etoricoxib
Authorised
2010-08-06
PACKAGE LEAFLET: INFORMATION FOR THE USER ARCOXIA® 60 mg film-coated tablets ARCOXIA® 90 mg film-coated tablets etoricoxib 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 ARCOXIA is and what it is used for 2. What you need to know before you take ARCOXIA 3. How to take ARCOXIA 4. Possible side effects 5. How to store ARCOXIA 6. Contents of the pack and other information 1. WHAT ARCOXIA IS AND WHAT IT IS USED FOR WHAT IS ARCOXIA? • ARCOXIA contains the active substance etoricoxib. ARCOXIA is one of a group of medicines called selective COX-2 inhibitors. These belong to a family of medicines called non-steroidal anti-inflammatory drugs (NSAIDs). WHAT IS ARCOXIA USED FOR? • ARCOXIA helps to reduce the pain and swelling (inflammation) in the joints and muscles of people 16 years of age and older with osteoarthritis, rheumatoid arthritis, ankylosing spondylitis and gout. • ARCOXIA is also used for the short-term treatment of moderate pain after dental surgery in people 16 years of age and older. WHAT IS OSTEOARTHRITIS? Osteoarthritis is a disease of the joints. It results from the gradual breakdown of cartilage that cushions the ends of the bones. This causes swelling (inflammation), pain, tenderness, stiffness and disability. WHAT IS RHEUMATOID ARTHRITIS? Rheumatoid arthritis is a long-term inflammatory disease of the joints. It causes pain, stiffness, swelling, and increasing loss of movement in the joints it affects. It may also cause inflammation in other areas of the body. WHAT I Прочитайте повний документ
Health Products Regulatory Authority 30 November 2021 CRN00CP6X Page 1 of 2 SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT Arcoxia 90 mg film-coated tablets 2 QUALITATIVE AND QUANTITATIVE COMPOSITION Each film-coated tablet contains 90 mg of etoricoxib. Excipients with known effect: 90 mg tablet: 4.0 mg lactose For the full list of excipients, see section 6.1. 3 PHARMACEUTICAL FORM Film-coated tablet (tablets). _Product imported from Romania_: White, apple shaped, biconvex film-coated tablets debossed '202' on one side and 'ARCOXIA 90' on the other side 4 CLINICAL PARTICULARS As per PA0964/009/003 5 PHARMACOLOGICAL PROPERTIES As per PA0964/009/003 6 PHARMACEUTICAL PARTICULARS 6.1 LIST OF EXCIPIENTS _Core:_ Calcium hydrogen phosphate (anhydrous) Croscarmellose sodium Magnesium stearate Microcrystalline cellulose _Tablet Coating:_ Carnauba wax Lactose monohydrate Hypromellose Titanium dioxide (E171) Triacetin 6.2 INCOMPATIBILITIES Not applicable. Health Products Regulatory Authority 30 November 2021 CRN00CP6X Page 2 of 2 6.3 SHELF LIFE The shelf-life expiry date of this product is the date shown on the blister strips and outer carton of the product on the market in the country of origin. 6.4 SPECIAL PRECAUTIONS FOR STORAGE Store below 25° C. Store in the original package in order to protect from moisture. 6.5 NATURE AND CONTENTS OF CONTAINER Aluminium/aluminium blisters in over-labelled cardboard cartons containing 28 tablets. 6.6 SPECIAL PRECAUTIONS FOR DISPOSAL AND OTHER HANDLING No special requirements 7 PARALLEL PRODUCT AUTHORISATION HOLDER IMED Healthcare Ltd. Unit 625 Kilshane Avenue Northwest Business Park Ballycoolin Dublin 15 Ireland 8 PARALLEL PRODUCT AUTHORISATION NUMBER PPA1463/041/002 9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION Date of first authorisation: 6 th August 2010 10 DATE OF REVISION OF THE TEXT November 2021 Прочитайте повний документ