Stribild Európska únia - taliančina - EMA (European Medicines Agency)

stribild

gilead sciences ireland uc - elvitegravir, cobicistat, emtricitabina, tenofovir disoproxil fumarato - infezioni da hiv - antivirals for treatment of hiv infections, combinations, antivirals for systemic use - trattamento del virus dell'immunodeficienza umana 1 (hiv-1) infezione in adulti età compresa tra 18 anni e oltre che sono naïve al trattamento antiretrovirale o sono infettate con hiv 1 senza mutazioni note associate a resistenza ad uno qualsiasi dei tre agenti antiretrovirali in stribild.

Harvoni Európska únia - taliančina - EMA (European Medicines Agency)

harvoni

gilead sciences ireland uc - ledipasvir, sofosbuvir - epatite c, cronica - antivirali per uso sistemico - harvoni is indicated for the treatment of chronic hepatitis c (chc) in adult and paediatric patients aged 3 years and above (see sections 4. 2, 4. 4 e 5. per il virus dell'epatite c (hcv) di genotipo-specifici di attività, vedere sezioni 4. 4 e 5.

Refixia Európska únia - taliančina - EMA (European Medicines Agency)

refixia

novo nordisk a/s - nonacog beta pegol - emofilia b - antiemorragici - trattamento e profilassi delle emorragie in pazienti con emofilia b (congenita carenza di fattore ix). , refixia can be used for all age groups.

Apealea Európska únia - taliančina - EMA (European Medicines Agency)

apealea

inceptua ab - paclitaxel - neoplasie ovariche - antineoplastic agents, taxanes - apealea in combinazione con carboplatino è indicato per il trattamento di pazienti adulti con prima recidiva platino‑sensibile cancro epiteliale ovarico, cancro peritoneale primario e di tuba di falloppio cancro.

Zynlonta Európska únia - taliančina - EMA (European Medicines Agency)

zynlonta

swedish orphan biovitrum ab - loncastuximab tesirine - lymphoma, large b-cell, diffuse; lymphoma, b-cell - agenti antineoplastici - zynlonta as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large b-cell lymphoma (dlbcl) and high-grade b-cell lymphoma (hgbl), after two or more lines of systemic therapy.

Clopidogrel Viatris (previously Clopidogrel Taw Pharma) Európska únia - taliančina - EMA (European Medicines Agency)

clopidogrel viatris (previously clopidogrel taw pharma)

viatris limited - clopidogrel besilate - peripheral vascular diseases; stroke; myocardial infarction - 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), ischemic 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 infarto miocardico acuto, in combinazione con asa in medicalmente trattati i pazienti eleggibili per la terapia trombolitica. 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. per ulteriori informazioni, si prega di fare riferimento alla sezione 5.

Hemangiol Európska únia - taliančina - EMA (European Medicines Agency)

hemangiol

pierre fabre medicament - propranololo cloridrato - emangioma - agenti beta-bloccanti - hemangiol is indicated in the treatment of proliferating infantile haemangioma requiring systemic therapy: , life- or function-threatening haemangioma,, ulcerated haemangioma with pain and/or lack of response to simple wound care measures,, haemangioma with a risk of permanent scars or disfigurement. , it is to be initiated in infants aged 5 weeks to 5 months.

Iblias Európska únia - taliančina - EMA (European Medicines Agency)

iblias

bayer ag - octocog alfa - emofilia a - antiemorragici - trattamento e profilassi del sanguinamento in pazienti con emofilia a (deficit di fattore viii congenito). iblias può essere utilizzato per tutti i gruppi di età.

Ioa Európska únia - taliančina - EMA (European Medicines Agency)

ioa

n.v. organon - nomegestrol acetato di estradiolo - contraccezione - ormoni sessuali e modulatori del sistema genitale, - contraccezione orale.

Zepatier Európska únia - taliančina - EMA (European Medicines Agency)

zepatier

merck sharp & dohme b.v. - elbasvir, grazoprevir - epatite c, cronica - direct acting antivirals, antivirals for systemic use, antivirals for treatment of hcv infections - zepatier is indicated for the treatment of chronic hepatitis c (chc) in adult and paediatric patients 12 years of age and older who weigh at least 30 kg (see sections 4. 2, 4. 4 e 5. per il virus dell'epatite c (hcv) di genotipo-specifici di attività, vedere sezioni 4. 4 e 5.