Norge -
norsk -
Statens legemiddelverk
metastron 150 mbq
ge healthcare b.v. - strontium (89sr) klorid - injeksjonsvæske, oppløsning - 150 mbq
Norge -
norsk -
Statens legemiddelverk
cefazolin mip 2 g
mip pharma gmbh - cefazolinnatrium - pulver til injeksjons-/infusjonsvæske, oppløsning - 2 g
Den europeiske union -
norsk -
EMA (European Medicines Agency)
ultomiris
alexion europe sas - ravulizumab - hemoglobinuri, paroksysmal - selektive immunosuppressiva - 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.
Den europeiske union -
norsk -
EMA (European Medicines Agency)
caspofungin accord
accord healthcare s.l.u. - caspofunginacetat - candidiasis; aspergillosis - antimykotika for systemisk bruk - behandling av invasiv candidiasis i voksen eller paediatric pasienter. behandling av invasive aspergillosis i voksen eller paediatric pasienter som er refraktære til eller intolerante av amfotericin b, lipid formuleringer av amfotericin b og/eller itrakonazol. refraktivitet er definert som progresjon av infeksjon eller unnlatelse av å forbedre etter minimum 7 dager før terapeutiske doser av effektive soppdrepende behandling. empirisk behandling for antatte fungal infeksjoner (for eksempel candida eller aspergillus) i febrile, neutropaenic voksen eller paediatric pasienter.
Den europeiske union -
norsk -
EMA (European Medicines Agency)
cancidas (previously caspofungin msd)
merck sharp & dohme b.v. - caspofungin (as acetate) - candidiasis; aspergillosis - antimykotika for systemisk bruk - 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.
Den europeiske union -
norsk -
EMA (European Medicines Agency)
ceprotin
takeda manufacturing austria ag - humant protein c - purpura fulminans; protein c deficiency - antithrombotic agents - 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.
Den europeiske union -
norsk -
EMA (European Medicines Agency)
zoledronic acid teva generics
teva generics b.v - zoledronsyre monohydrat - osteoporosis; osteitis deformans - bisfosfonater - behandling av osteoporosisin post-menopausal womenin voksen menat økt risiko for brudd, inkludert de med nyere lav-traumer hoftebrudd. behandling av osteoporose forbundet med langvarig systemisk glukokortikoid therapyin post-menopausal womenin voksen menat økt risiko for brudd. behandling av pagets sykdom i beinet i voksne.
Den europeiske union -
norsk -
EMA (European Medicines Agency)
clynav
elanco gmbh - puk-spdv-poly2#1 dna-plasmider koding for salmon pancreas disease virus proteiner - immunologicals for atlantisk laks, - atlanterhavslaks - for den aktive vaksinering av atlantisk laks for å redusere nedsatt daglig vektøkning, og redusere dødelighet, og hjerte -, pankreas og skjelettmuskulatur lesjoner forårsaket av bukspyttkjertel sykdom etter infeksjon med laksefisk alphavirus undertype 3 (sav3).