Norge - norsk - Statens legemiddelverk

roche norge as - benserazidhydroklorid / levodopa - depotkapsel, hard - 25 mg / 100 mg

Norge - norsk - Statens legemiddelverk

roche norge as - benserazidhydroklorid / levodopa - oppløselig tablett - 12.5 mg / 50 mg

Norge - norsk - Statens legemiddelverk

janssen-cilag as - galantaminhydrobromid - depotkapsel, hard - 16 mg

Norge - norsk - Statens legemiddelverk

janssen-cilag as - galantaminhydrobromid - depotkapsel, hard - 8 mg

Norge - norsk - Statens legemiddelverk

janssen-cilag as - galantaminhydrobromid - depotkapsel, hard - 24 mg

Norge - norsk - Statens legemiddelverk

orifarm as - galantaminhydrobromid - depotkapsel, hard - 16 mg

Norge - norsk - Statens legemiddelverk

macure pharma aps - oksybutyninhydroklorid - tablett - 5 mg

Den europeiske union - norsk - EMA (European Medicines Agency)

takeda pharma a/s - brentuximab vedotin - lymphoma, non-hodgkin; hodgkin disease - antineoplastiske midler - hodgkin lymphomaadcetris is indicated for adult patients with previously untreated cd30+ stage iv hodgkin lymphoma (hl) in combination with doxorubicin, vinblastine and dacarbazine (avd). adcetris is indicated for the treatment of adult patients with cd30+ hl at increased risk of relapse or progression following autologous stem cell transplant (asct). adcetris is indicated for the treatment of adult patients with relapsed or refractory cd30+ hodgkin lymphoma (hl):following asct, orfollowing at least two prior therapies when asct or multi-agent chemotherapy is not a treatment option. systemic anaplastic large cell lymphomaadcetris in combination with cyclophosphamide, doxorubicin and prednisone (chp) is indicated for adult patients with previously untreated systemic anaplastic large cell lymphoma (salcl). adcetris is indicated for the treatment of adult patients with relapsed or refractory salcl. cutaneous t cell lymphomaadcetris is indicated for the treatment of adult patients with cd30+ cutaneous t cell lymphoma (ctcl) after at least 1 prior systemic therapy.

Den europeiske union - norsk - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - belimumab - lupus erythematosus, systemisk - immunsuppressive - benlysta er angitt som add-on terapi hos pasienter i alderen 5 år og eldre med aktiv, autoantistoffer positiv systemisk lupus erythematosus (sle), med en høy grad av sykdomsaktivitet (e. positive anti-dsdna og lav komplement) til tross for at standard terapi. benlysta is indicated in combination with background immunosuppressive therapies for the treatment of adult patients with active lupus nephritis.

Den europeiske union - norsk - EMA (European Medicines Agency)

upjohn eesv - pregabalin - epilepsy; anxiety disorders; neuralgia - antiepileptics, , andre antiepileptics - nevropatisk painlyrica er angitt for behandling av perifer og sentral nevropatisk smerte hos voksne. epilepsylyrica er indisert som tilleggsbehandling hos voksne med partielle anfall med eller uten sekundær generalisering. generell angst disorderlyrica er angitt for behandling av generalisert angstlidelse (gad) i voksne.