Calcitriol Salmon Pharma 0,5 ug Capsule সুইজারল্যান্ড - ইতালীয় - Swissmedic (Swiss Agency for Therapeutic Products)

calcitriol salmon pharma 0,5 ug capsule

salmon pharma gmbh - calcitriolum - capsule - calcitriolum 0.5 µg, triglycerida media, e 320, e 321, kapselhülle: gelatina, glycerolum (85 per centum), sorbitolum liquidum partim deshydricum corresp. sorbitolum 2.7-4.32 mg, e 172 (rubrum), pro capsula. - renale osteodystrophie, ipoparatiroidismo, rachitismo, osteoporosi post-menopausa - synthetika

METOXSALENE G.L. PHARMA ইতালী - ইতালীয় - AIFA (Agenzia Italiana del Farmaco)

metoxsalene g.l. pharma

g.l. pharma gmbh - altre citochine e immunomodulatori - altre citochine e immunomodulatori

Clopidogrel Hexal ইউরোপীয় ইউনিয়ন - ইতালীয় - EMA (European Medicines Agency)

clopidogrel hexal

acino pharma gmbh - clopidogrel - peripheral vascular diseases; acute coronary syndrome; myocardial infarction; stroke - agenti antitrombotici - clopidogrel è indicato negli adulti per la prevenzione di eventi atherothrombotic in:pazienti affetti da infarto miocardico (da pochi giorni fino a meno di 35 giorni), ictus ischemico (da 7 giorni fino a meno di 6 mesi) o accertata malattia arteriosa periferica;i pazienti affetti da sindrome coronarica acuta:- camere non-st segment elevation sindrome coronarica acuta (angina instabile o non-q infarto miocardico), inclusi pazienti sottoposti a posizionamento di stent in seguito a intervento coronarico percutaneo, in associazione con acido acetilsalicilico (asa);- st segment elevation infarto miocardico acuto, in combinazione con asa in medicalmente trattati i pazienti eleggibili per la terapia trombolitica. per ulteriori informazioni, si prega di fare riferimento alla sezione 5.

Clopidogrel Taw Pharma (previously Clopidogrel Mylan) ইউরোপীয় ইউনিয়ন - ইতালীয় - EMA (European Medicines Agency)

clopidogrel taw pharma (previously clopidogrel mylan)

taw pharma (ireland) limited - clopidogrel cloridrato - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - agenti antitrombotici - , , , , secondary prevention of atherothrombotic events, , clopidogrel is indicated in: , - adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease. , - adult patients suffering from acute coronary syndrome:,    - non-st segment elevation acute coronary syndrome (unstable angina or non-q-wave myocardial infarction), including patients undergoing a stent placement following percutaneous coronary intervention, in combination with acetylsalicylic acid (asa). ,     - st segment elevation acute myocardial infarction, in combination with asa in medically treated patients eligible for thrombolytic therapy. , , in patients with moderate to high-risk transient ischaemic attack (tia) or minor ischaemic stroke (is), clopidogrel in combination with asa is indicated in:, - adult patients with moderate to high-risk tia (abcd2  score ≥4) or minor is (nihss  ≤3) within 24 hours of either the tia or is event.  , , prevention of atherothrombotic and thromboembolic events in atrial fibrillation, in adult patients with atrial fibrillation who have at least one risk factor for vascular events, are not suitable for treatment with vitamin k antagonists (vka) and who have a low bleeding risk, clopidogrel is indicated in combination with asa for the prevention of atherothrombotic and thromboembolic events, including stroke. , , for further information please refer to section 5. , , ,.

Clopidogrel Sandoz ইউরোপীয় ইউনিয়ন - ইতালীয় - EMA (European Medicines Agency)

clopidogrel sandoz

acino pharma gmbh - clopidogrel - peripheral vascular diseases; stroke; myocardial infarction - agenti antitrombotici - clopidogrel è indicato negli adulti per la prevenzione di eventi aterotrombotici in: * pazienti affetti da infarto miocardico (da pochi giorni fino a meno di 35), ischemico (da 7 giorni fino a meno di 6 mesi) o stabilito periferico malattia arteriosa. per ulteriori informazioni, si prega di fare riferimento alla sezione 5.

Pioglitazone Teva Pharma ইউরোপীয় ইউনিয়ন - ইতালীয় - EMA (European Medicines Agency)

pioglitazone teva pharma

teva pharma b.v. - pioglitazone cloridrato - diabete mellito, tipo 2 - farmaci usati nel diabete - pioglitazone is indicated in the treatment of type-2 diabetes mellitus as monotherapy: , in adult patients (particularly overweight patients) inadequately controlled by diet and exercise for whom metformin is inappropriate because of contraindications or intolerance. , pioglitazone is also indicated for combination with insulin in type 2 diabetes mellitus adult patients with insufficient glycaemic control on insulin for whom metformin is inappropriate because of contraindications or intolerance. dopo l'inizio della terapia con pioglitazone, i pazienti devono essere rivisti dopo 3 a 6 mesi per valutare l'adeguatezza della risposta al trattamento (e. riduzione dell'hba1c). nei pazienti che non mostrano una risposta adeguata, pioglitazone deve essere interrotto. alla luce di potenziali rischi di un prolungato di terapia, i medici prescrittori devono confermare alla successiva routine di recensioni che il beneficio di pioglitazone è mantenuto.