Imovane 7.5 mg Norvegia - norvegiană - Statens legemiddelverk

imovane 7.5 mg

sanofi-aventis norge (3) - zopiklon - tablett, filmdrasjert - 7.5 mg

Ropivacain Fresenius Kabi 5 mg/ ml Norvegia - norvegiană - Statens legemiddelverk

ropivacain fresenius kabi 5 mg/ ml

fresenius kabi norge as - halden - ropivakainhydrokloridmonohydrat - injeksjonsvæske, oppløsning - 5 mg/ ml

Visipaque 320 mg I/ ml Norvegia - norvegiană - Statens legemiddelverk

visipaque 320 mg i/ ml

ge healthcare as - jodiksanol - injeksjonsvæske, oppløsning - 320 mg i/ ml

Visipaque 270 mg I/ ml Norvegia - norvegiană - Statens legemiddelverk

visipaque 270 mg i/ ml

ge healthcare as - jodiksanol - injeksjonsvæske, oppløsning - 270 mg i/ ml

Zopiklon Mylan 5 mg Norvegia - norvegiană - Statens legemiddelverk

zopiklon mylan 5 mg

mylan ab - zopiklon - tablett, filmdrasjert - 5 mg

Zopiklon Mylan 7.5 mg Norvegia - norvegiană - Statens legemiddelverk

zopiklon mylan 7.5 mg

mylan ab - zopiklon - tablett, filmdrasjert - 7.5 mg

Fixopost 50 mikrog/ ml / 5 mg/ ml Norvegia - norvegiană - Statens legemiddelverk

fixopost 50 mikrog/ ml / 5 mg/ ml

laboratoires thea s.a.s - latanoprost / timololmaleat - Øyedråper, oppløsning i endosebeholder - 50 mikrog/ ml / 5 mg/ ml

Jayempi Uniunea Europeană - norvegiană - EMA (European Medicines Agency)

jayempi

nova laboratories ireland limited - azathioprine - graft-avvisning - immunsuppressive - jayempi is indicated in combination with other immunosuppressive agents for the prophylaxis of transplant rejection in patients receiving allogenic kidney, liver, heart, lung or pancreas transplants. azathioprine is indicated in immunosuppressive regimens as an adjunct to immunosuppressive agents that form the mainstay of treatment (basis immunosuppression). jayempi is used as an immunosuppressant antimetabolite either alone or, more commonly, in combination with other agents (usually corticosteroids) and/ or procedures which influence the immune response. jayempi is indicated in patients who are intolerant to glucocorticosteroids or if the therapeutic response is inadequate despite treatment with high doses of glucocorticosteroids, in the following diseases:severe active rheumatoid arthritis (chronic polyarthritis) that cannot be kept under control by less toxic agents (disease-modifying anti-rheumatic -medicinal products – dmards)auto-immune hepatitis systemic lupus erythematosusdermatomyositispolyarteritis nodosapemphigus vulgaris and bullous pemphigoidbehçet’s diseaserefractory auto-immune haemolytic anaemia, caused by warm igg antibodieschronic refractory idiopathic thrombocytopenic purpurajayempi is used for the treatment of moderately severe to severe forms of chronic inflammatory bowel disease (ibd) (crohn’s disease or ulcerative colitis) in patients in whom glucocorticosteroid therapy is necessary, but where glucocorticosteroids are not tolerated, or in whom the disease is untreatable with other common means of first choice. it is also indicated in adult patients in relapsing multiple sclerosis, if an immunomodulatory therapy is indicated but beta interferon therapy is not possible, or a stable course has been achieved with previous treatment with azathioprine. 3jayempi is indicated for the treatment of generalised myasthenia gravis. depending on the severity of the disease, jayempi should be given in combination with glucocorticosteroids because of slow onset of action at the beginning of treatment and the glucocorticosteroid dose should be gradually reduced after several months of treatment.

Yesafili Uniunea Europeană - norvegiană - EMA (European Medicines Agency)

yesafili

viatris limited - aflibercept - macular edema; retinal vein occlusion; diabetic retinopathy; myopia, degenerative; diabetes complications - Øyemidler - yesafili is indicated for adults for the treatment ofneovascular (wet) age-related macular degeneration (amd) (see section 5. 1),visual impairment due to macular oedema secondary to retinal vein occlusion (branch rvo or central rvo) (see section 5. 1),visual impairment due to diabetic macular oedema (dme) (see section 5. 1),visual impairment due to myopic choroidal neovascularisation (myopic cnv) (see section 5.

Genvoya Uniunea Europeană - norvegiană - EMA (European Medicines Agency)

genvoya

gilead sciences ireland uc - elvitegravir, cobicistat, emtricitabine, tenofovir alafenamide - hiv-infeksjoner - antivirale midler til systemisk bruk - genvoya er indisert for behandling av voksne og ungdom (12 år og eldre med kropp vekt minst 35 kg) infisert med humant immunsviktvirus 1 (hiv-1) uten noen kjente mutasjoner tilknyttet motstand mot integrase hemmer klassen, emtricitabine eller tenofovir.