Fingolimod Accord Den europeiske union - norsk - EMA (European Medicines Agency)

fingolimod accord

accord healthcare s.l.u. - fingolimod hydrochloride - multippel sklerose, relapsing-remitting - immunosuppressants, selektiv immunosuppressants - angitt som enkelt sykdom endre terapi i svært aktive relapsing remitting multippel sklerose for følgende grupper av voksne pasienter og paediatric pasienter i alderen 10 år og eldre:pasienter med svært aktiv sykdom til tross for en fullstendig og adekvat løpet av behandlingen med minst én sykdom endre therapyorpatients med raskt utviklende alvorlig relapsing remitting multippel sklerose definert ved 2 eller flere deaktivere tilbakefall i ett år, og med 1 eller flere gadolinium å styrke lesjoner på brain mr eller en betydelig økning i t2 lesjon legg i forhold til en tidligere nyere mr.

Fingolimod Mylan Den europeiske union - norsk - EMA (European Medicines Agency)

fingolimod mylan

mylan ireland limited - fingolimod hydrochloride - multippel sklerose, relapsing-remitting - immunsuppressive - 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 og 5. 1)orpatients med raskt utviklende alvorlig relapsing remitting multippel sklerose definert ved 2 eller flere deaktivere tilbakefall i ett år, og med 1 eller flere gadolinium å styrke lesjoner på brain mr eller en betydelig økning i t2 lesjon legg i forhold til en tidligere nyere mr.

Fingolimod Mylan Den europeiske union - norsk - EMA (European Medicines Agency)

fingolimod mylan

mylan ireland limited - fingolimod hydrochloride - multippel sklerose, relapsing-remitting - immunsuppressive - 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 og 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.

Dimethyl fumarate Mylan Den europeiske union - norsk - EMA (European Medicines Agency)

dimethyl fumarate mylan

mylan ireland limited - dimetylfumarat - multippel sklerose, relapsing-remitting - immunsuppressive - dimethyl fumarate mylan is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Dimethyl fumarate Polpharma Den europeiske union - norsk - EMA (European Medicines Agency)

dimethyl fumarate polpharma

zaklady farmafarmaceutyczne polpharma s.aceutyczne polpharma s.a. - dimetylfumarat - multippel sklerose, relapsing-remitting - immunsuppressive - dimethyl fumarate polpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Dimethyl fumarate Teva Den europeiske union - norsk - EMA (European Medicines Agency)

dimethyl fumarate teva

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

Dimethyl fumarate Sandoz 240 mg Norge - norsk - Statens legemiddelverk

dimethyl fumarate sandoz 240 mg

sandoz a/s - dimetylfumarat - enterokapsel, hard - 240 mg

Dimethyl fumarate Sandoz 120 mg Norge - norsk - Statens legemiddelverk

dimethyl fumarate sandoz 120 mg

sandoz a/s - dimetylfumarat - enterokapsel, hard - 120 mg

Dimethyl fumarate Accord Den europeiske union - norsk - EMA (European Medicines Agency)

dimethyl fumarate accord

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

Dimethyl fumarate Glenmark 240 mg Norge - norsk - Statens legemiddelverk

dimethyl fumarate glenmark 240 mg

glenmark arzneimittel gmbh - dimetylfumarat - enterokapsel, hard - 240 mg