Norge -
norsk -
Statens legemiddelverk
provocholine 100 mg
acic europe limited - metakolinklorid - pulver til inhalasjonsvæske til nebulisator, oppløsning - 100 mg
Den europeiske union -
norsk -
EMA (European Medicines Agency)
yselty
theramex ireland limited - linzagolix choline - leiomyomer - hypofysiske og hypotalamiske hormoner og analoger - yselty is indicated for the treatment of moderate to severe symptoms of uterine fibroids in adult women of reproductive age.
Den europeiske union -
norsk -
EMA (European Medicines Agency)
rivastigmine 3m health care ltd
3m health care limited - rivastigmin - alzheimers sykdom - psychoanaleptics, , anticholinesterases - symptomatisk behandling av mild til moderat alvorlig alzheimers demens.
Norge -
norsk -
Statens legemiddelverk
plaquenil 200 mg
sanofi-aventis norge (3) - hydroksyklorokinsulfat - tablett, filmdrasjert - 200 mg
Norge -
norsk -
Statens legemiddelverk
robinul 0.2 mg/ ml
viatris as - glykopyrroniumbromid - injeksjonsvæske, oppløsning - 0.2 mg/ ml
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.