GLYCOPYRRONIUM-NEOSTIGMINE süstelahus Estonie - estonien - Ravimiamet

glycopyrronium-neostigmine süstelahus

b. braun melsungen ag - neostigmiin+glükopürroonium - süstelahus - 2,5mg+0,5mg 1ml 1ml 10tk

WATER FOR INJECTION süsteravimi lahusti Estonie - estonien - Ravimiamet

water for injection süsteravimi lahusti

b. braun melsungen ag - süstevesi - süsteravimi lahusti - 1000ml 1tk

ETOMIDATE-LIPURO süsteemulsioon Estonie - estonien - Ravimiamet

etomidate-lipuro süsteemulsioon

b. braun melsungen ag - etomidaat - süsteemulsioon - 2mg 1ml 10ml 10tk

Pandemic Influenza Vaccine H5N1 Baxter AG Union européenne - estonien - EMA (European Medicines Agency)

pandemic influenza vaccine h5n1 baxter ag

resilience biomanufacturing ireland limited - antigeen, mis sisaldab: a / vietnam / 1203/2004 (h5n1), gripivaktsiin (kogu virion, inaktiveeritud) - influenza, human; immunization; disease outbreaks - vaktsiinid - gripi profülaktika ametlikult pandeemia korral. pandeemilise gripi vaktsiini tuleks kasutada vastavalt ametlikele juhistele.

GENTAMICIN B.BRAUN infusioonilahus Estonie - estonien - Ravimiamet

gentamicin b.braun infusioonilahus

b.braun medical, s.a. - gentamütsiin - infusioonilahus - 3mg 1ml 80ml 10tk

GENTAMICIN B.BRAUN infusioonilahus Estonie - estonien - Ravimiamet

gentamicin b.braun infusioonilahus

b.braun medical, s.a. - gentamütsiin - infusioonilahus - 1mg 1ml 80ml 10tk

Ceprotin Union européenne - estonien - EMA (European Medicines Agency)

ceprotin

takeda manufacturing austria ag - inimese valk c - purpura fulminans; protein c deficiency - antitrombootilised ained - ceprotin is indicated for prophylaxis and treatment of  purpura fulminans  coumarin-induced skin necrosis and venous thrombotic events in patients with severe congenital protein c deficiency.

Clopidogrel Acino Union européenne - estonien - EMA (European Medicines Agency)

clopidogrel acino

acino ag - klopidogreel - peripheral vascular diseases; acute coronary syndrome; myocardial infarction; stroke - antitrombootilised ained - clopidogrel is indicated in adults for the prevention of atherothrombotic events in: , , , 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, 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, patients suffering from acute coronary syndrome. , ,.

Iblias Union européenne - estonien - EMA (European Medicines Agency)

iblias

bayer ag - octocog alfa - hemofiilia a. - antihemorraagilised ained - verejooksu ravi ja profülaktika hemofiilia a patsientidel (kaasasündinud viii faktori puudulikkus). iblias võib kasutada kõikides vanuserühmades.