Ország: Egyesült Királyság
Nyelv: angol
Forrás: MHRA (Medicines & Healthcare Products Regulatory Agency)
Bendroflumethiazide
RX Farma
C03AA01
Bendroflumethiazide
5mg
Oral tablet
Oral
No Controlled Drug Status
Valid as a prescribable product
BNF: 02020100; GTIN: 5060637640210
Continued, please turn over SPECIAL TRIM Package leaflet: Information for the Patient BENDROFLUMETHIAZIDE 2.5MG TABLETS BENDROFLUMETHIAZIDE 5MG TABLETS (BENDROFLUMETHIAZIDE) This medicine will be called Bendroflumethiazide Tablets in this leaflet. 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, pharmacist or nurse. • This medicine is only for you. Do not pass it to others. It may harm them, even if their signs of illness are the same as yours. • If you get any of the side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. See section 4. WHAT IS IN THIS LEAFLET: 1. What Bendroflumethiazide Tablets is and what it is used for 2. What you need to know before you take Bendroflumethiazide Tablets 3. How to take Bendroflumethiazide Tablets 4. Possible side effects 5. How to store Bendroflumethiazide Tablets 6. Contents of the pack and other information 1. What Bendroflumethiazide Tablets is and what it is used for These tablets are available in two different strengths, 2.5mg and 5mg and your doctor will have decided which is the most suitable for you. Bendroflumethiazide belongs to a group of medicines called diuretics (water tablets) which increase urine production. Bendroflumethiazide Tablets are used to treat hypertension (high blood pressure) and oedema (fluid retention) associated with such conditions as kidney disorder, liver damage, heart failure and premenstrual fluid retention. 2. What you need to know before you take Bendroflumethiazide Tablets DO NOT TAKE BENDROFLUMETHIAZIDE TABLETS: • If you ever had an allergic reaction to bendroflumethiazide or any other ingredients of this medicine (allergic reactions include mild symptoms such as itching and/or rash. More severe symptoms include swelling of the face, lips, tongue and/or throat with difficulty in swa Olvassa el a teljes dokumentumot
SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT Bendroflumethiazide 5mg Tablets 2 QUALITATIVE AND QUANTITATIVE COMPOSITION Each tablet contains Bendroflumethiazide 5mg. For a full list of excipients, see section 6.1. 3 PHARMACEUTICAL FORM Tablets for oral use. White, circular flat faced tablets with bevelled edges, B 5 separated by a break line on one face and plain on the reverse. 4 CLINICAL PARTICULARS 4.1 THERAPEUTIC INDICATIONS Bendroflumethiazide is a diuretic. The tablets are indicated for the treatment of essential hypertension and oedema associated with such conditions as nephrotic syndrome, cirrhosis of the liver, congestive heart failure and pre- menstrual oedema. 4.2 POSOLOGY AND METHOD OF ADMINISTRATION _Adults: _ Oedema 5-10mg daily in the morning initially. Maintenance: usually 2.5mg-5mg on only two or three days in the week. A single dose may be sufficient Essential Hypertension 2.5mg in the morning. Doses above 2.5mg are rarely necessary. Pre-menstrual syndrome 2.5mg each morning for seven days before the period is due. _ _ _Children:_ Oedema Up to 400 micrograms per kg body weight daily initially, reducing to 50-100 micrograms per kg for maintenance. Elderly: The dosage of thiazide diuretics may need to be reduced in the elderly, particularly when renal function is impaired, because of the possibility of electrolyte imbalance.” 4.3 CONTRAINDICATIONS Bendroflumethiazide tablets are contraindicated in patients with known hypersensitivity to thiazides; hypercalcaemia, hyponatraemia, refractory hypokalemia, severe renal and hepatic insufficiency, symptomatic hyperuricaemia and Addison's disease. 4.4 SPECIAL WARNINGS AND PRECAUTIONS FOR USE HYPOKALAEMIA Electrolytes should be monitored during treatment as continued or intensive use of bendroflumethiazide may result in hypokalaemia. This effect may be enhanced with concomitant use of medicines that can also cause hypokalaemia such as other diuretics or beta-2 agonists. Hypokalaemia can increase the risk of cardiac arrhythmia partic Olvassa el a teljes dokumentumot