Europeiska unionen - svenska - EMA (European Medicines Agency)

eli lilly nederland b.v. - mirikizumab - kolit, ulcerativ - immunsuppressiva - omvoh is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a biologic treatment.

Europeiska unionen - svenska - EMA (European Medicines Agency)

sanofi winthrop industrie - teriflunomide - multipel skleros - selektiva immunsuppressiva medel - aubagio is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 for important information on the population for which efficacy has been established).

Europeiska unionen - svenska - EMA (European Medicines Agency)

immunocore ireland limited - tebentafusp - uveal neoplasms - antineoplastiska medel - kimmtrak is indicated as monotherapy for the treatment of human leukocyte antigen (hla)-a*02:01-positive adult patients with unresectable or metastatic uveal melanoma.

Europeiska unionen - svenska - EMA (European Medicines Agency)

mylan pharmaceuticals limited - teriflunomide - multipel skleros, skovvis förlöpande - immunsuppressiva - teriflunomide mylan is indicated for the treatment of adult patients and paediatric patients aged 10 years and older (body weight > 40 kg) with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 of the smpc for important information on the population for which efficacy has been established).

Europeiska unionen - svenska - EMA (European Medicines Agency)

accord healthcare s.l.u. - teriflunomide - multipel skleros, skovvis förlöpande - immunsuppressiva, selektiva immunsuppressiva - teriflunomide accord is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 for important information on the population for which efficacy has been established).

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

newbury pharmaceuticals ab - teriflunomid - filmdragerad tablett - 14 mg - laktosmonohydrat hjälpämne; teriflunomid 14 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

sandoz a/s - teriflunomid - filmdragerad tablett - 14 mg - allurarött ac aluminiumlack hjälpämne; laktosmonohydrat hjälpämne; teriflunomid 14 mg aktiv substans; glycerol hjälpämne

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

stada arzneimittel ag - teriflunomid - filmdragerad tablett - 14 mg - teriflunomid 14 mg aktiv substans; laktosmonohydrat hjälpämne

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

zentiva k.s. - teriflunomid - filmdragerad tablett - 14 mg - laktosmonohydrat hjälpämne; teriflunomid 14 mg aktiv substans

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

avansor pharma oy - teriflunomid - filmdragerad tablett - 14 mg - teriflunomid 14 mg aktiv substans; laktosmonohydrat hjälpämne