NATALIZUMAB - Meklēšanas rezultāti

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

natalizumab elan pharma

elan pharma international ltd. - natalizumab - krona slimība - imunitātes stimulatori, - Ārstēšana mēreni līdz stipri aktīvs krona slimība samazināšanas pazīmes un simptomi, un indukcijas un apkope ilgstošu atbildi un atlaišanu, pacientiem, kuriem nav atbildējis, neskatoties uz pilnu un atbilstošu terapijas kurss ar kortikosteroīdu un immunosuppressant; vai nepanes vai ir medicīniskās kontrindikācijas, lai šādu terapiju.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

tyruko

sandoz gmbh - natalizumab - multiple sclerosis, relapsing-remitting; multiple sclerosis - imūnsupresanti - 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 un 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.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

tysabri

biogen netherlands b.v. - natalizumab - multiplā skleroze - selective immunosuppressants - 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 un 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.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

dimethyl fumarate neuraxpharm

laboratorios lesvi s.l. - dimethyl fumarate - multiplā skleroze, recidivējoši-pārskaitot - imūnsupresanti - dimethyl fumarate neuraxpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.