NovoSeven Evropska unija - slovenščina - EMA (European Medicines Agency)

novoseven

novo nordisk a/s - eptakog alfa (aktiviran) - hemophilia b; thrombasthenia; factor vii deficiency; hemophilia a - antihemoragije - novoseven je primerna za zdravljenje epizod krvavitev in preprečevanju krvavitev v teh kirurških posegov ali invazivnih postopkih v naslednjih bolnik skupine:pri bolnikih s prirojeno hemofilija z inhibitorji za koagulacije faktorjev viii ali ix > 5 bethesda enot (bu);pri bolnikih s prirojeno hemofilija, ki se pričakuje, da imajo visoko anamnestic odziv na faktor viii ali faktor ix uprave;pri bolnikih z pridobljena hemofilija;pri bolnikih s prirojeno faktor vii pomanjkljivosti;pri bolnikih z glanzmann je thrombasthenia z protiteles za trombocitov glikoprotein (gp) iib-iiia in / ali človeške leucocyte antigenov (hla), in s preteklo ali sedanjo refractoriness, da transfuzije trombocitov. pri bolnikih z glanzmann je thrombasthenia s preteklo ali sedanjo refractoriness, da transfuzije trombocitov, ali če trombocitov niso na voljo.

Cancidas (previously Caspofungin MSD) Evropska unija - slovenščina - EMA (European Medicines Agency)

cancidas (previously caspofungin msd)

merck sharp & dohme b.v. - caspofungin (as acetate) - candidiasis; aspergillosis - antimikotiki za sistemsko uporabo - treatment of invasive candidiasis in adult or paediatric patients;treatment of invasive aspergillosis in adult or paediatric patients who are refractory to or intolerant of amphotericin b, lipid formulations of amphotericin b and / or itraconazole. refractoriness is defined as progression of infection or failure to improve after a minimum of seven days of prior therapeutic doses of effective antifungal therapy;empirical therapy for presumed fungal infections (such as candida or aspergillus) in febrile, neutropaenic adult or paediatric patients.

Plavix Evropska unija - slovenščina - EMA (European Medicines Agency)

plavix

sanofi winthrop industrie - klopidogrel vodikov sulfat - stroke; peripheral vascular diseases; atrial fibrillation; myocardial infarction; acute coronary syndrome - antitrombotična sredstva - secondary prevention of atherothrombotic eventsclopidogrel is indicated in:adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from seven days until less than six 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 patients undergoing percutaneous coronary intervention (including patients undergoing a stent replacement) or medically treated patients eligible for thrombolytic/fibrinolytic therapy. in patients with moderate to high-risk transient ischemic attack (tia) or minor ischemic 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. preprečevanje atherothrombotic in thromboembolic dogodkov v atrijska fibrillationin odraslih bolnikov z atrijsko fibrilacijo, ki imajo vsaj en dejavnik tveganja za žilne dogodke, niso primerni za zdravljenje z vitaminom k antagonisti in ki imajo nizko tveganje krvavitve, clopidogrel je indiciran v kombinaciji s asa za preprečevanje atherothrombotic in thromboembolic dogodkov, vključno z možgansko kap.

Cevenfacta Evropska unija - slovenščina - EMA (European Medicines Agency)

cevenfacta

laboratoire francais du fractionnement et des biotechnologies - eptacog beta (activated) - hemophilia a; hemophilia b - antihemoragije - cevenfacta is indicated in adults and adolescents (12 years of age and older) for the treatment of bleeding episodes and for the prevention of bleeding in those undergoing surgery or invasive procedures in the following patient groups:in patients with congenital haemophilia with high-responding inhibitors to coagulation factors viii or ix (i. ≥5 bethesda units (bu)); in patients with congenital haemophilia with low titre inhibitors (bu.

Prevenar 13 Evropska unija - slovenščina - EMA (European Medicines Agency)

prevenar 13

pfizer europe ma eeig - pneumococcal polysaccharide serotype 1, pneumococcal polysaccharide serotype 3, pneumococcal polysaccharide serotype 4, pneumococcal polysaccharide serotype 5, pneumococcal polysaccharide serotype 6a, pneumococcal polysaccharide serotype 6b, pneumococcal polysaccharide serotype 7f, pneumococcal polysaccharide serotype 9v, pneumococcal polysaccharide serotype 14, pneumococcal polysaccharide serotype 18c, pneumococcal polysaccharide serotype 19a, pneumococcal polysaccharide serotype 19f, pneumococcal polysaccharide serotype 23f - pneumococcal infections; immunization - cepiva - aktivna imunizacija za preprečevanje invazivne bolezni, pljučnice in akutnega srednjega ušesa, ki jo povzroča streptococcus pneumoniae pri dojenčkih, otrocih in mladostnikih od 6. do 17. leta starosti. aktivno imunizacijo za preprečevanje invazivnih bolezni, ki jih povzroča streptococcus pneumoniae pri odraslih ≥18 let in starejši. glej poglavja 4. 4 in 5. 1 za informacije o zaščiti proti specifičnim pnevmokoknim serotipom. uporaba prevenar 13 je treba določiti na podlagi uradnih priporočil, ob upoštevanju tveganja invazivnih bolezni v različnih starostnih skupinah, osnovna comorbidities kot tudi variabilnost serotip epidemiologija v različnih geografskih področjih,.

Prevenar Evropska unija - slovenščina - EMA (European Medicines Agency)

prevenar

pfizer limited - pneumococcal oligosaccharide serotype 18c, pneumococcal polysaccharide serotype 19f, pneumococcal polysaccharide serotype 23f, pneumococcal polysaccharide serotype 4, pneumococcal polysaccharide serotype 6b, pneumococcal polysaccharide serotype 9v, pneumococcal polysaccharide serotype 14 - pneumococcal infections; immunization - cepiva - aktivne imunizacije proti bolezni, ki povzroča streptococcus pneumoniae serotipe 4, 6b, iz 9v, 14, 18 c, 19f in 23f (vključno s sepso, meningitisom, pljučnica, bakteriemija in akutni otitis media) pri dojenčkih in otrocih od dveh mesecev do petih let starosti. uporaba prevenar je treba določiti na podlagi uradnih priporočil, ob upoštevanju vpliva invazivnih bolezni v različnih starostnih skupin, kot tudi variabilnost serotip epidemiologija v različnih geografskih področjih,.