Teriflunomide Mylan Unión Europea - español - EMA (European Medicines Agency)

teriflunomide mylan

mylan pharmaceuticals limited - teriflunomide - la esclerosis múltiple remitente-recurrente - inmunosupresores - 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).

Teriflunomide Accord Unión Europea - español - EMA (European Medicines Agency)

teriflunomide accord

accord healthcare s.l.u. - teriflunomide - la esclerosis múltiple remitente-recurrente - los inmunosupresores selectivos de inmunosupresores - 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).

Dimethyl fumarate Teva Unión Europea - español - EMA (European Medicines Agency)

dimethyl fumarate teva

teva gmbh - fumarato de dimetilo - multiple sclerosis, relapsing-remitting; multiple sclerosis - inmunosupresores - dimethyl fumarate teva is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

FUMARATO DE DIMETILO KERN PHARMA 120 MG CAPSULAS DURAS GASTRORRESISTENTES EFG España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

fumarato de dimetilo kern pharma 120 mg capsulas duras gastrorresistentes efg

kern pharma s.l. - fumarato de dimetilo - cÁpsula dura gastrorresistente - 120 mg - fumarato de dimetilo 120 mg - dimetil fumarato

FUMARATO DE DIMETILO KERN PHARMA 240 MG CAPSULAS DURAS GASTRORRESISTENTES EFG España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

fumarato de dimetilo kern pharma 240 mg capsulas duras gastrorresistentes efg

kern pharma s.l. - fumarato de dimetilo - cÁpsula dura gastrorresistente - 240 mg - fumarato de dimetilo 240 mg - dimetil fumarato

FUMARATO DE DIMETILO SANDOZ 120 MG CAPSULAS DURAS GASTRORRESISTENTES EFG España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

fumarato de dimetilo sandoz 120 mg capsulas duras gastrorresistentes efg

sandoz farmaceutica s.a. - fumarato de dimetilo - cÁpsula dura gastrorresistente - 120 mg - fumarato de dimetilo 120 mg - dimetil fumarato

FUMARATO DE DIMETILO SANDOZ 240 MG CAPSULAS DURAS GASTRORRESISTENTES EFG España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

fumarato de dimetilo sandoz 240 mg capsulas duras gastrorresistentes efg

sandoz farmaceutica s.a. - fumarato de dimetilo - cÁpsula dura gastrorresistente - 240 mg - fumarato de dimetilo 240 mg - dimetil fumarato

Dimethyl fumarate Accord Unión Europea - español - EMA (European Medicines Agency)

dimethyl fumarate accord

accord healthcare s.l.u. - fumarato de dimetilo - multiple sclerosis, relapsing-remitting; multiple sclerosis - inmunosupresores - dimethyl fumarate accord is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

TERIFLUNOMIDA SANDOZ 14 MG COMPRIMIDOS RECUBIERTOS CON PELICULA EFG España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

teriflunomida sandoz 14 mg comprimidos recubiertos con pelicula efg

sandoz farmaceutica s.a. - teriflunomida - comprimido recubierto con pelÍcula - 14 mg - teriflunomida 14 mg - teriflunomida

Tyruko Unión Europea - español - EMA (European Medicines Agency)

tyruko

sandoz gmbh - natalizumab - multiple sclerosis, relapsing-remitting; multiple sclerosis - inmunosupresores - 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 y 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.