Země: Velká Británie
Jazyk: angličtina
Zdroj: MHRA (Medicines & Healthcare Products Regulatory Agency)
Terazosin hydrochloride
Sigma Pharmaceuticals Plc
G04CA03
Terazosin hydrochloride
10mg
Oral tablet
Oral
No Controlled Drug Status
Valid as a prescribable product
BNF: 02050400
306/06 TERAZOSIN 2 MG, 5MG AND 10MG TABLETS 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 or nurse. 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 or nurse. This includes any possible side effects not listed in this leaflet. See section 4. WHAT IS IN THIS LEAFLET: 1. What Terazosin is and what it is used for 2. What you need to know before you take Terazosin 3. How to take Terazosin 4. Possible side effects 5. How to store Terazosin 6. Contents of the pack and other information 1. WHAT TERAZOSIN IS AND WHAT IT IS USED FOR The name of this medicine is Terazosin 2mg Tablets, Terazosin 5mg Tablets or Terazosin 10mg Tablets referred to as Terazosin throughout this leaflet. Terazosin belongs to a group of medicines called ‘alpha blockers’ which help to relax smooth muscle and has been prescribed for you to treat one of the following: Improve the obstructive symptoms caused by benign prostatic hyperplasia (BPH) and help the flow of urine from the bladder Treat mild to moderate hypertension (high blood pressure). 2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE TERAZOSIN DO NOT TAKE TERAZOSIN IF: You are allergic (hypersensitive) to Terazosin or to any of the other ingredients in this medicine (listed in Section 6) You are allergic (hypersensitive) to other medicines in the ‘alpha blocker’ group. You have ever fallen over or fainted whilst passing water. Do not take Terazosin if any of the above apply to you. If you are not sure, talk to your doctor or pharmacist before taking this medicine. WARNINGS AND PRECAUTIONS Talk to your doctor or pharmacist before taking Terazosin if you: Are taking other medication for high blood pressu Přečtěte si celý dokument
SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT Terazosin Teva 10 mg Tablets 2 QUALITATIVE AND QUANTITATIVE COMPOSITION Each tablet contains 11.87mg of terazosin hydrochloride dihydrate equivalent to 10 mg of terazosin. Excipient with known effect: Each 10 mg tablet contains 109.03 mg lactose monohydrate. For the full list of excipients, see section 6.1. 3 PHARMACEUTICAL FORM Tablet Mottled blue, round, flat tablet with bevelled edges embossed with “93” on one-side and “763” on the other side. 4 CLINICAL PARTICULARS 4.1 THERAPEUTIC INDICATIONS Terazosin Teva Tablets are indicated for: The treatment of mild to moderate hypertension. The symptomatic treatment of urinary obstruction caused by benign prostatic hyperplasia (BPH). 4.2 POSOLOGY AND METHOD OF ADMINISTRATION For oral use. For the different dosage regimens suitable strengths are available. The dose of terazosin should be adjusted according to the patient's response. The following is a guide to administration: INITIAL DOSE The lowest single dose of 1 mg before bedtime for all patients which should not be exceeded. Strict compliance with this recommendation should be observed to minimise potential acute first-dose hypotensive episodes. SUBSEQUENT DOSES Treatment of mild to moderate hypertension. The single daily dosage may be increased by approximately doubling the dosage at weekly intervals to achieve the desired blood pressure response. The maintenance dose needs to be adjusted to the patient’s response. 2 mg/day may be sufficient with increases up to 10 mg if necessary (clinical studies support the use of 2 – 10 mg as maintenance dose). The maximum dose is 20 mg of terazosin per day and should not be exceeded. Use with thiazide diuretics and other antihypertensive agents in the treatment of hypertension When adding a thiazide diuretic or another antihypertensive agent to a patient's regimen the dose of terazosin should be reduced or discontinued and retitration carried out if necessary. Caution should be observed when terazo Přečtěte si celý dokument