Euroopa Liit - eesti - EMA (European Medicines Agency)

elan pharma international ltd. - natalisumab - crohni tõbi - immunostimulants, - ravi mõõduka kuni raske aktiivse crohni tõbi vähendamise nähud ja sümptomid, ja induktsiooni ja hooldus püsiva reageerimise ja remissiooni, patsientidel, kes ei ole vastanud vaatamata täielikku ja piisavat käigus ravi kortikosteroidide ja immunosuppressant; või ei talu või on meditsiinilised vastunäidustused, et selline ravi.

Euroopa Liit - eesti - EMA (European Medicines Agency)

biogen netherlands b.v. - natalisumab - hulgiskleroos - selektiivsed immunosupressandid - 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.

Euroopa Liit - eesti - EMA (European Medicines Agency)

sandoz gmbh - natalisumab - multiple sclerosis, relapsing-remitting; multiple sclerosis - immunosupressandid - 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.

Euroopa Liit - eesti - EMA (European Medicines Agency)

laboratorios lesvi s.l. - dimetüülfumaraat - sclerosis multiplex, relapsing-remitting - immunosupressandid - dimethyl fumarate neuraxpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Eesti - eesti - Ravimiamet

g.l. pharma gmbh - fingolimood - kõvakapsel - 0,5mg 10tk; 0,5mg 28tk; 0,5mg 60tk; 0,5mg 30tk; 0,5mg 98tk; 0,5mg 7tk

Eesti - eesti - Ravimiamet

norameda uab - fingolimood - kõvakapsel - 0,5mg 28tk; 0,5mg 98tk; 0,5mg 100tk

Eesti - eesti - Ravimiamet

grindeks as - fingolimood - kõvakapsel - 0,5mg 28tk

Eesti - eesti - Ravimiamet

zentiva k.s. - fingolimood - kõvakapsel - 0,5mg 28tk; 0,5mg 30tk; 0,5mg 7tk; 0,5mg 56tk

Eesti - eesti - Ravimiamet

teva gmbh - fingolimood - kõvakapsel - 0,5mg 10tk; 0,5mg 98tk; 0,5mg 28tk; 0,5mg 100tk; 0,5mg 30tk

Eesti - eesti - Ravimiamet

medochemie limited - fingolimood - kõvakapsel - 0,5mg 98tk; 0,5mg 28tk; 0,5mg 7tk; 0,5mg 10tk; 0,5mg 30tk