Land: Malta
Sprache: Englisch
Quelle: Medicines Authority
SILDENAFIL CITRATE
Zentiva k.s. U kabelovny 130, Dolní Mecholupy, 102 37 Praha 10, Czech Republic
G04BE03
SILDENAFIL CITRATE 20 mg
FILM-COATED TABLET
SILDENAFIL CITRATE 20 mg
POM
UROLOGICALS
Withdrawn
2017-04-18
PAGE 1 OF 7 PACKAGE LEAFLET: INFORMATION FOR THE PATIENT SILDENAFIL ZENTIVA 20 MG FILM-COATED TABLETS sildenafil 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 Sildenafil Zentiva is and what it is used for 2. What you need to know before you take Sildenafil Zentiva 3. How to take Sildenafil Zentiva 4. Possible side effects 5. How to store Sildenafil Zentiva 6. Contents of the pack and other information 1. WHAT SILDENAFIL ZENTIVA IS AND WHAT IT IS USED FOR Sildenafil Zentiva contains the active substance sildenafil which belongs to a group of medicines called phosphodiesterase type 5 (PDE5) inhibitors. Sildenafil Zentiva brings down blood pressure in the lungs by widening the blood vessels in the lungs. Sildenafil Zentiva is used to treat adults and children and adolescents from 1 to 17 years old with high blood pressure in the blood vessels in the lungs (pulmonary arterial hypertension). 2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE SILDENAFIL ZENTIVA DO NOT TAKE SILDENAFIL ZENTIVA IF YOU − are allergic to sildenafil or any of the other ingredients of this medicine (listed in section 6). − are taking medicines containing nitrates, or nitric oxide donors such as amyl nitrate (“poppers”). These medicines are often given for relief of chest pain (or “angina pectoris”). PAGE 2 OF 7 Sildenafil Zentiva can cause a serious increase in the effects of these medicines. Tell your doctor if you are taking any of these medicines. If you are not certain, ask your doctor or pharmacist. − are Lesen Sie das vollständige Dokument
PAGE 1 OF 22 SUMMARY OF PRODUCT CHARACTERISTICS 1. NAME OF THE MEDICINAL PRODUCT Sildenafil Zentiva 20 mg film-coated tablets 2. QUALITATIVE AND QUANTITATIVE COMPOSITION Each film-coated tablet contains 20 mg sildenafil (as citrate). For the full list of excipients, see section 6.1. 3. PHARMACEUTICAL FORM Film-coated tablet. White to off-white, round, lens-shape, film-coated tablets. 4. CLINICAL PARTICULARS 4.1 THERAPEUTIC INDICATIONS Adults Treatment of adult patients with pulmonary arterial hypertension classified as WHO functional class II and III, to improve exercise capacity. Efficacy has been shown in primary pulmonary hypertension and pulmonary hypertension associated with connective tissue disease. Paediatric population Treatment of paediatric patients aged 1 year to 17 years old with pulmonary arterial hypertension. Efficacy in terms of improvement of exercise capacity or pulmonary haemodynamics has been shown in primary pulmonary hypertension and pulmonary hypertension associated with congenital heart disease (see section 5.1). 4.2 POSOLOGY AND METHOD OF ADMINISTRATION Treatment should only be initiated and monitored by a physician experienced in the treatment of pulmonary arterial hypertension. In case of clinical deterioration in spite of Sildenafil Zentiva treatment, alternative therapies should be considered. PAGE 2 OF 22 Posology _Adults _ The recommended dose is 20 mg three times a day (TID). Physicians should advise patients who forget to take Sildenafil Zentiva to take a dose as soon as possible and then continue with the normal dose. Patients should not take a double dose to compensate for the missed dose. _Paediatric population (1 year to 17 years) _ For paediatric patients aged 1 year to 17 years old, the recommended dose in patients ≤ 20 kg is 10 mg three times a day and for patients > 20 kg is 20 mg three times a day. Higher than recommended doses should not be used in paediatric patients with PAH (see also sections 4.4 and 5.1). The 20 mg tablet should not be used in cases where 10 mg TI Lesen Sie das vollständige Dokument