Euroopan unioni -
suomi -
EMA (European Medicines Agency)
tysabri
biogen netherlands b.v. - natalitsumabin - multippeliskleroosi - selektiiviset immunosuppressantit - tysabri is indicated as single disease modifying therapy in adults with highly active relapsing remitting multiple sclerosis for the following patient groups: , patients with highly active disease activity despite a full and adequate course of treatment with at least one disease modifying therapy (dmt) (for exceptions and information about washout periods see sections 4. 4 ja 5. 1), , or, patients with rapidly evolving severe relapsing remitting multiple sclerosis defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain mri or a significant increase in t2 lesion load as compared to a previous recent mri.
Euroopan unioni -
suomi -
EMA (European Medicines Agency)
lumeblue (previously known as methylthioninium chloride cosmo)
alfasigma s.p.a. - metyylitioniniumkloridia - colorectal neoplasms; colonoscopy - other diagnostic agents - lumeblue is indicated as a diagnostic agent enhancing visualisation of colorectal lesions in adult patients undergoing screening or surveillance colonoscopy.
Euroopan unioni -
suomi -
EMA (European Medicines Agency)
fingolimod mylan
mylan ireland limited - fingolimod hydrochloride - multippeliskleroosi, relapsoiva-remittoiva - immunosuppressantit - indicated as single disease modifying therapy in highly active relapsing remitting multiple sclerosis for the following groups of adult and paediatric patients aged 10 years and older: patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (for exceptions and information about washout periods see sections 4. 4 ja 5. 1) or patients with rapidly evolving severe relapsing remitting multiple sclerosis defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain mri or a significant increase in t2 lesion load as compared to a previous recent mri.
Euroopan unioni -
suomi -
EMA (European Medicines Agency)
tyruko
sandoz gmbh - natalitsumabin - multiple sclerosis, relapsing-remitting; multiple sclerosis - immunosuppressantit - tyruko is indicated as single disease modifying therapy in adults with highly active relapsing remitting multiple sclerosis (rrms) for the following patient groups: patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (dmt) (for exceptions and information about washout periods see sections 4. 4 ja 5. 1), or, patients with rapidly evolving severe rrms defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain magnetic resonance imaging (mri) or a significant increase in t2 lesion load as compared to a previous recent mri.
Euroopan unioni -
suomi -
EMA (European Medicines Agency)
xigris
eli lilly nederland b.v. - drotrekogiini alfa (aktivoitu) - sepsis; multiple organ failure - antitromboottiset aineet - xigris on tarkoitettu aikuispotilaille, joilla on vaikea sepsis, ja useiden elinten vikoja, kun sitä lisätään parhaaseen vakiotilaan. xigrisin käyttöä tulee harkita pääasiassa tilanteissa, joissa hoito voidaan aloittaa 24 tunnin kuluttua elimen vajaatoiminnan alkamisesta (lisätietoja on kohdassa 5.