Страна: Нідерланди
мова: голландська
Джерело: CBG-MEB (College ter Beoordeling van Geneesmiddelen)
DUTASTERIDE
Regiomedica GmbH
G04CB02
DUTASTERIDE
Capsule, zacht
BUTYLHYDROXYTOLUEEN (E 321) ; GELATINE (E 441) ; GLYCEROL (E 422) ; GLYCEROL MONOCAPRYLOCAPRAAT, TYPE I ; IJZEROXIDE GEEL (E 172) ; IJZEROXIDE ROOD (E 172) ; TITAANDIOXIDE (E 171),
Oraal gebruik
Dutasteride
Hulpstoffen: BUTYLHYDROXYTOLUEEN (E 321); GELATINE (E 441); GLYCEROL (E 422); GLYCEROL MONOCAPRYLOCAPRAAT, TYPE I; IJZEROXIDE GEEL (E 172); IJZEROXIDE ROOD (E 172); TITAANDIOXIDE (E 171);
2014-01-20
PACKAGE LEAFLET: INFORMATION FOR THE USER DUTASTERIDE REGIOMEDICA 0.5 MG CAPSULES, SOFT dutasteride 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. - 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 Dutasteride Regiomedica is and what it is used for 2. What you need to know before you take Dutasteride Regiomedica 3. How to take Dutasteride Regiomedica 4. Possible side effects 5. How to store Dutasteride Regiomedica 6. Contents of the pack and other information 1. WHAT DUTASTERIDE REGIOMEDICA IS AND WHAT IT IS USED FOR DUTASTERIDE REGIOMEDICA IS USED TO TREAT MEN WITH AN ENLARGED PROSTATE _(benign prostatic _ _hyperplasia)_ - a non-cancerous growth of the prostate gland, caused by producing too much of a hormone called dihydrotestosterone. The active ingredient is dutasteride. It belongs to a group of medicines called 5-alpha reductase inhibitors. As the prostate grows, it can lead to urinary problems, such as difficulty in passing urine and a need to go to the toilet frequently. It can also cause the flow of the urine to be slower and less forceful. If left untreated, there is a risk that your urine flow will be completely blocked _(acute urinary retention)_ . This requires immediate medical treatment. In some situations surgery is necessary to remove or reduce the size of the prostate gland. Dutasteride Regiomedica lowers the production of dihydrotestosterone, which helps to shrink the prostate and relieve the symptoms. This will reduce the risk of acute urinary retention and the need for surgery. Dutasteride Regiomedica may also be used with a Прочитайте повний документ
SUMMARY OF PRODUCT CHARACTERISTICS 1. NAME OF THE MEDICINAL PRODUCT Dutasteride Regiomedica 0.5 mg capsules, soft 2. QUALITATIVE AND QUANTITATIVE COMPOSITION Each capsule contains 0.5 mg dutasteride. For the full list of excipients, see section 6.1. 3. PHARMACEUTICAL FROM Capsule, soft. Dutasteride Regiomedica soft capsules are light brown, oblong soft-gelatin capsules without printing, approximately 19 x 7 mm, containing a clear, slightly yellow to pale amber, oily liquid. 4. CLINICAL PARTICULARS 4.1 THERAPEUTIC INDICATIONS Treatment of moderate to severe symptoms of benign prostatic hyperplasia (BPH). Reduction in the risk of acute urinary retention (AUR) and surgery in patients with moderate to severe symptoms of BPH. For information on effects of treatment and patient populations studied in clinical trials please see section 5.1. 4.2 POSOLOGY AND METHOD OF ADMINISTRATION Dutasteride Regiomedica can be administered alone or in combination with the alpha-blocker tamsulosin (0.4 mg) (see sections 4.4, 4.8 and 5.1). _ _ POSOLOGY Adults (including elderly): The recommended dose of Dutasteride Regiomedica is one capsule (0.5 mg) taken orally once a day. The capsules should be swallowed whole and not chewed or opened as contact with the capsule contents may result in irritation of the oropharyngeal mucosa. The capsules may be taken with or without food. Although an improvement may be observed at an early stage, it can take up to 6 months before a response to the treatment can be achieved. No dose adjustment is necessary in the elderly. Renal impairment The effect of renal impairment on dutasteride pharmacokinetics has not been studied. No adjustment in dosage is anticipated for patients with renal impairment (see section 5.2). Hepatic impairment The effect of hepatic impairment on dutasteride pharmacokinetics has not been studied so caution should be used in patients with mild to moderate hepatic impairment (see sections 4.4 and 5.2). In patients with severe hepatic impairment, the use of dutasteride is contraindica Прочитайте повний документ