Krajina: Írsko
Jazyk: angličtina
Zdroj: HPRA (Health Products Regulatory Authority)
BISOPROLOL HEMIFUMARATE
PCO Manufacturing
C07AB07
BISOPROLOL HEMIFUMARATE
1.25 Milligram
Film Coated Tablet
Product subject to prescription which may be renewed (B)
Beta blocking agents, selective
Authorised
2008-01-25
_ _ PACKAGE LEAFLET: INFORMATION FOR THE USER CARDICOR ® 1.25 MG FILM-COATED TABLETS CARDICOR ® 2.5 MG FILM-COATED TABLETS bisoprolol fumarate 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 your 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 Cardicor is and what it is used for 2. What you need to know before you take Cardicor 3. How to take Cardicor 4. Possible side effects 5. How to store Cardicor 6. Contents of the pack and other information 1. WHAT CARDICOR IS AND WHAT IT IS USED FOR The active substance in Cardicor is bisoprolol. Bisoprolol belongs to a group of medicines called beta-blockers. These medicines work by affecting the body’s response to some nerve impulses, especially in the heart. As a result, bisoprolol slows down the heart rate and makes the heart more efficient at pumping blood around the body. Heart failure occurs when the heart muscle is weak and unable to pump enough blood to supply the body’s needs. Cardicor is used to treat stable chronic heart failure. It is used in combination with other medicines suitable for this condition (such as ACE-inhibitors, diuretics, and heart glycosides). 2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE CARDICOR DO NOT TAKE CARDICOR Do not take Cardicor if one of the following conditions applies to you: Allergy (hypersensitivity) to bisoprolol or to Prečítajte si celý dokument
SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT Cardicor 1.25mg Film-coated tablets 2 QUALITATIVE AND QUANTITATIVE COMPOSITION Each tablet contains 1.25 mg bisoprolol fumarate. For a full list of excipients, see section 6.1. 3 PHARMACEUTICAL FORM Film-coated tablet _The product imported from Italy, The United Kingdom and Germany:_ White, round film-coated tablets 4 CLINICAL PARTICULARS As per PA0654/007/001 5 PHARMACOLOGICAL PROPERTIES As per PA0654/007/001 6 PHARMACEUTICAL PARTICULARS 6.1 LIST OF EXCIPIENTS Product imported from Italy and the United Kingdom Tablet Core: Silica, Colloidal anhydrous Magnesium Stearate Crospovidone Pregelatinised maize starch Maize starch Microcrystalline cellulose Calcium hydrogen phosphate, anhydrous. Film coating: Dimeticone Talc Macrogol 400 Titanium dioxide (E171) Hypromellose. Product imported from Germany Silica, Colloidal anhydrous Magnesium (stearate, palmitate, oleat) Crospovidone Pregelatinised starch Maize starch HEALTH PRODUCTS REGULATORY AUTHORITY ________________________________________________________________________________________________________________________ _Date Printed 04/03/2016_ _CRN 2174066_ _page number: 1_ Microcrystalline cellulose Calcium hydrogen phosphate Dimeticone Talc Macrogol 400 Titanium dioxide (E171) Hypromellose 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 package of the product on the market in the country of origin. 6.4 SPECIAL PRECAUTIONS FOR STORAGE Do not store above 25°C. 6.5 NATURE AND CONTENTS OF CONTAINER The immediate container is a blister, which is packaged in an outer carton. Pack size: 28 or 30 tablets. Not all pack sizes may be marketed. 6.6 SPECIAL PRECAUTIONS FOR DISPOSAL OF A USED MEDICINAL PRODUCT OR WASTE MATERIALS DERIVED FROM Prečítajte si celý dokument