‘SORBITRATE’ ORAL TABLETS |
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WHAT YOU SHOULD KNOW ABOUT 'SORBITRATE' The information in this leaflet applies only to your medicine 'Sorbitrate', please read it carefully. It gives you important information but it can't tell you everything. If you have any questions, or are not sure about anything, ask your doctor or pharmacist. WHAT IS YOUR MEDICINE? 'Sorbitrate' comes as tablets and each contains either 10mg or 20mg of isosorbide dinitrate. Each tablet contains a number of inactive ingredients which allow it to be made. These are: lactose, magnesium stearate, starch, pregelatinized starch. 'Sorbitrate' 10mg tablets also contain quinoline yellow and 'Sorbitrate' 20mg tablets also contain brilliant blue FCF. 'Sorbitrate' 10mg comes in containers of 100 and 500 tablets. 'Sorbitrate' 20mg comes in containers of 100 tablets. 'Sorbitrate' belongs to a group of medicines called vasodilators. This means that it has effects on the blood vessels within your body, and can cause both the veins and arteries to dilate, increasing the size of these blood vessels. These blood vessels can therefore carry more blood around the body and in particular to the heart. WHO HAS MADE YOUR MEDICINE? The product licence holder and manufacturer of 'Sorbitrate' is: ZENECA Limited Macclesfield Cheshire United Kingdom
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WHAT IS YOUR MEDICINE FOR? ‘Sorbitrate’ is used to prevent the onset of angina (chest pain) and in combination with other drugs. It is used to treat heart failure. WHEN SHOULD ‘SORBITRATE’ NOT BE USED?
you have ever shown an allergic reaction to 'Sorbitrate' or to any other medicines containing either isosorbide dinitrate or isosorbide mononitrate. you suffer from a very low blood pressure or have recently suffered from a heart attack.
WHAT PRECAUTIONS SHOULD BE TAKEN WITH 'SORBITRATE’?
you are pregnant or are breast feeding. you are taking any other medicines including those which you have bought. In particular tell your doctor if you are taking any medicines for the treatment of high blood pressure (hypertension).
HOW SHOULD I TAKE MY 'SORBITRATE’?
WHAT UNDESIRABLE EVENTS MAY BE EXPERIENCED WITH 'SORBITRATE’? As with all medicines undesirable events are sometimes experienced. With 'Sorbitrate' these may include:
These may occur at the start of treatment but tend to become less as treatment continues. Other effects which may occur less frequently include:
Do not be alarmed by this list of possible events. You may not have any of them. Tell your doctor or pharmacist d you think you have any of these or any other problems with your tablets. HOW SHOULD I STORE 'SORBITRATE’?
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Date of preparation of leaflet: June 1995 ‘Sorbitrate’ is a trade mark, the property of ZENECA Limited 8/IE/UK/1015680 |
P2135746 |