Uniunea Europeană - finlandeză - EMA (European Medicines Agency)

sanofi-aventis deutschland gmbh - glargininsuliini - diabetes mellitus - diabeetilla käytettävät lääkkeet - diabetes mellituksen hoitoon aikuisille, nuorille ja lapsille 6-vuotiaille.

Finlanda - finlandeză - Fimea (Suomen lääkevirasto)

fresenius kabi ab - aspartic acid, glutamic acid, alanine, arginine, calcium chloride dihydrate, glucose monohydrate, aminoacetic acid, histidine, isoleucine, potassium chloride, leucine, methionine, phenylalanine, proline, serine, threonine, tryptophane, tyrosine, valine, lysine hydrochloride, magnesium sulfate heptahydrate, sodium acetate trihydrate, sodium glycerophosphate anhydrous, soya oil - infuusioneste, emulsio - yhdistelmävalmisteet

Finlanda - finlandeză - Fimea (Suomen lääkevirasto)

fresenius kabi ab - aspartic acid, glutamic acid, alanine, arginine, calcium chloride dihydrate, glucose monohydrate, aminoacetic acid, histidine, isoleucine, potassium chloride, leucine, methionine, phenylalanine, proline, serine, threonine, tryptophane, tyrosine, valine, lysine hydrochloride, magnesium sulfate heptahydrate, sodium acetate trihydrate, sodium glycerophosphate anhydrous, soya oil - infuusioneste, emulsio - yhdistelmävalmisteet

Uniunea Europeană - finlandeză - EMA (European Medicines Agency)

roche registration ltd. - ibandronihappo - osteoporoosi, postmenopausaalinen - lääkkeet luusairauksien hoitoon - osteoporoosin hoito menopausian jälkeisissä naisilla lisääntyneen murtumisvaaran vuoksi. vähentää nikamamurtumien riskiä on osoitettu. tehoa on reisiluun kaulan murtumia ei ole osoitettu.

Uniunea Europeană - finlandeză - EMA (European Medicines Agency)

roche registration ltd. - daklitsumabia - graft rejection; kidney transplantation - immunosuppressantit - zenapax on tarkoitettu akuutin hylkimisreaktion de novo allogenic munuaisten transplantaation ennaltaehkäisyyn ja käytetään samanaikaisesti immunosuppressiivinen hoito, kuten siklosporiinin ja kortikosteroidien potilailla, jotka heitä, erittäin ovat ole rokotettu.

Finlanda - finlandeză - Fimea (Suomen lääkevirasto)

fresenius kabi ab - flumazenil - injektioneste, liuos - 0.1 mg/ml - flumatseniili

Finlanda - finlandeză - Fimea (Suomen lääkevirasto)

fresenius kabi ab - alanine, arginine, calcium chloride dihydrate, glucose monohydrate, aminoacetic acid, histidine, isoleucine, potassium chloride, leucine, lysine acetate, methionine, phenylalanine, proline, serine, threonine, tryptophane, tyrosine, valine, magnesium sulfate heptahydrate, taurine, triglycerides, medium-chain, zinc sulfate heptahydrate, soya-bean oil, refined, fish oil, rich in omega-3-acids, olive oil, refined, sodium glycerophosphate hydrate - infuusioneste, emulsio - yhdistelmävalmisteet

Finlanda - finlandeză - Fimea (Suomen lääkevirasto)

fresenius kabi ab - alanine, arginine, glucose monohydrate, aminoacetic acid, histidine, isoleucine, leucine, lysine acetate, methionine, phenylalanine, proline, serine, threonine, tryptophane, tyrosine, valine, taurine, triglycerides, medium-chain, soya-bean oil, refined, fish oil, rich in omega-3-acids, olive oil, refined - infuusioneste, emulsio - yhdistelmävalmisteet

Finlanda - finlandeză - Fimea (Suomen lääkevirasto)

fresenius kabi ab - alanine, arginine, calcium chloride dihydrate, glucose monohydrate, aminoacetic acid, histidine, isoleucine, potassium chloride, leucine, lysine acetate, methionine, proline, serine, threonine, tryptophane, tyrosine, valine, magnesium sulfate heptahydrate, sodium acetate trihydrate, taurine, zinc sulfate heptahydrate, triglycerides, medium-chain, soya-bean oil, refined, fish oil, rich in omega-3-acids, olive oil, refined, sodium glycerophosphate hydrate - infuusioneste, emulsio - yhdistelmävalmisteet

Uniunea Europeană - finlandeză - EMA (European Medicines Agency)

alexion europe sas - ravulizumab - hemoglobinuria, paroxysmal - selektiiviset immunosuppressantit - paroxysmal nocturnal haemoglobinuria (pnh)ultomiris is indicated in the treatment of adult and paediatric patients with a body weight of 10 kg or above with pnh:- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months (see section 5. atypical haemolytic uremic syndrome (ahus)ultomiris is indicated in the treatment of patients with a body weight of 10 kg or above with ahus who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab (see section 5. generalized myasthenia gravis (gmg)ultomiris is indicated as an add-on to standard therapy for the treatment of adult patients with gmg who are anti-acetylcholine receptor (achr) antibody-positive. neuromyelitis optica spectrum disorder (nmosd)ultomiris is indicated in the treatment of adult patients with nmosd who are anti-aquaporin 4 (aqp4) antibody-positive (see section 5. ultomiris is indicated in the treatment of adult patients with paroxysmal nocturnal haemoglobinuria (pnh):- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months. ultomiris is indicated in the treatment of adult patients with atypical haemolytic uremic syndrome (ahus) who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab.