الاتحاد الأوروبي - الإيطالية - EMA (European Medicines Agency)

biotest pharma gmbh - immunoglobulina umana da epatite b - immunization, passive; hepatitis b; liver transplantation - sieri immuni e immunoglobuline, - prevenzione della re-infezione da virus dell'epatite b (hbv) in pazienti adulti negativi con hbsag e hbv-dna almeno una settimana dopo il trapianto di fegato per insufficienza epatica indotta da epatite b. lo stato negativo di hbv-dna deve essere confermato negli ultimi 3 mesi precedenti l'olt. i pazienti devono essere hbsag negativi prima dell'inizio del trattamento. l'uso concomitante di adeguata virostatic agenti dovrebbero essere considerati come standard di epatite b re-infezione profilassi.

إيطاليا - الإيطالية - AIFA (Agenzia Italiana del Farmaco)

aristo pharma gmbh - desogestrel ed estrogeno - desogestrel ed estrogeno

إيطاليا - الإيطالية - AIFA (Agenzia Italiana del Farmaco)

pharmathen s.a. - voriconazolo - voriconazolo

الاتحاد الأوروبي - الإيطالية - EMA (European Medicines Agency)

axunio pharma gmbh - pirfenidone - fibrosi polmonare idiopatica - immunosoppressori - pirfenidone aet is indicated in adults for the treatment of mild to moderate idiopathic pulmonary fibrosis (ipf).

الاتحاد الأوروبي - الإيطالية - EMA (European Medicines Agency)

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. , , ,.

الاتحاد الأوروبي - الإيطالية - EMA (European Medicines Agency)

pari pharma gmbh - la tobramicina - cystic fibrosis; respiratory tract infections - antibatterici per uso sistemico, , antibatterici aminoglicosidici - vantobra è indicato per la gestione dell'infezione polmonare cronica dovuto pseudomonas aeruginosa in pazienti a partire dai 6 anni di età con fibrosi cistica (cf). dovrebbero essere prese in considerazione le linee guida ufficiali sull'uso appropriato degli agenti antibatterici..

الاتحاد الأوروبي - الإيطالية - EMA (European Medicines Agency)

zaklady farmafarmaceutyczne polpharma s.aceutyczne polpharma s.a. - dimetilfumarato - sclerosi multipla recidivante-remittente - immunosoppressori - dimethyl fumarate polpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

إيطاليا - الإيطالية - AIFA (Agenzia Italiana del Farmaco)

sandoz gmbh - enalapril e diuretici - enalapril e diuretici

إيطاليا - الإيطالية - AIFA (Agenzia Italiana del Farmaco)

aristo pharma gmbh - omeprazolo - omeprazolo

الاتحاد الأوروبي - الإيطالية - EMA (European Medicines Agency)

pinax pharma gmbh - ioflupane (123i) - radionuclide imaging; dementia; movement disorders - radiofarmaci diagnostici - questo medicinale è solo per uso diagnostico. celsunax is indicated for detecting loss of functional dopaminergic neuron terminals in the striatum:in adult patients with clinically uncertain parkinsonian syndromes, for example those with early symptoms, in order to help differentiate essential tremor from parkinsonian syndromes related to idiopathic parkinson’s disease, multiple system atrophy and progressive supranuclear palsy.  celsunax is unable to discriminate between parkinson's disease, multiple system atrophy and progressive supranuclear palsy. nei pazienti adulti, per aiutare a differenziare probabile demenza con corpi di lewy dal morbo di alzheimer.  celsunax is unable to discriminate between dementia with lewy bodies and parkinson’s disease dementia.