Quốc gia: Vương quốc Anh
Ngôn ngữ: Tiếng Anh
Nguồn: MHRA (Medicines & Healthcare Products Regulatory Agency)
Timolol maleate
DE Pharmaceuticals
S01ED01
Timolol maleate
2.5mg/1ml
Eye drops
Ocular
No Controlled Drug Status
Valid as a prescribable product
BNF: 11060000
1 PACKAGE LEAFLET: INFORMATION FOR THE PATIENT TIMOPTOL 0.25% W/V EYE DROPS, SOLUTION TIMOPTOL 0.5% W/V EYE DROPS, SOLUTION TIMOLOL (AS MALEATE) READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START USING 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 Timoptol is and what it is used for 2. What you need to know before you use Timoptol 3. How to use Timoptol 4. Possible side effects 5. How to store Timoptol 6. Contents of the pack and other information 1. WHAT TIMOPTOL IS AND WHAT IT IS USED FOR Timoptol contains a substance called timolol which belongs to a group of medicines called beta-blockers. Timolol lowers the pressure in your eye(s). It is used to treat glaucoma, when the pressure in the eye is raised. 2. WHAT YOU NEED TO KNOW BEFORE YOU USE TIMOPTOL DO NOT USE TIMOPTOL IF: you are allergic (hypersensitive) to timolol, beta-blockers or any of the other ingredients of Timoptol (see section 6: Contents of the pack and other information ) you have now or have had in the past respiratory problems such as asthma, severe chronic obstructive bronchitis (severe lung disease which may cause wheeziness, difficulty in breathing and/or long-standing cough) you have heart problems slow heart beat disorders of heart rhythm (irregular heart beats) heart failure - “cardiogenic shock” – a serious heart condition caused by very low blood pressure, which may result in the following symptoms: dizziness and lightheadedness, fast pulse rate, white skin, sweating, restlessness, loss of consciousness. If you are not sure whether you should Đọc toàn bộ tài liệu
SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT Timoptol 0.25% w/v eye drops, solution 2 QUALITATIVE AND QUANTITATIVE COMPOSITION Each millilitre of 0.5% w/v solution contains an amount of timolol maleate equivalent to 5 mg timolol. Excipients with known effect: Benzalkonium chloride 0.10 mg/ml Disodium phosphate dodecahydrate 30.42 mg/ml Sodium dihydrogen phosphate dihydrate 6.10 mg/ml. For the full list of excipients, see section 6.1. 3 PHARMACEUTICAL FORM Eye drops, solution. Clear, colourless to light yellow, sterile eye drops, solution. 4 CLINICAL PARTICULARS 4.1 THERAPEUTIC INDICATIONS Timoptol is a beta-adrenoreceptor blocking agent used topically in the reduction of elevated intra-ocular pressure in various conditions including following: patients with ocular hypertension; patients with chronic open-angle glaucoma including aphakic patients; some patients with secondary glaucoma. 4.2 POSOLOGY AND METHOD OF ADMINISTRATION Posology Recommended therapy is one drop 0.25% solution in the affected eye twice a day. If clinical response is not adequate, dosage may be changed to one drop 0.5% solution in each affected eye twice a day. If needed, Timoptol may be used with other agent(s) for lowering intra-ocular pressure. The use of two topical beta-adrenergic blocking agents is not recommended (see also section 4.4). Intra-ocular pressure should be reassessed approximately four weeks after starting treatment because response to Timoptol may take a few weeks to stabilise. Provided that the intra-ocular pressure is maintained at satisfactory levels, many patients can then be placed on once-a-day therapy. Transfer from other agents When another topical beta-blocking agent is being used, discontinue its use after a full day of therapy and start treatment with Timoptol the next day with one drop of 0.25% Timoptol in each affected eye twice a day. The dosage may be increased to one drop of 0.5% solution in each affected eye twice a day, if the response is not adequate. When transferring a patient from Đọc toàn bộ tài liệu