Dimethyl fumarate Polpharma Ευρωπαϊκή Ένωση - Λετονικά - EMA (European Medicines Agency)

dimethyl fumarate polpharma

zaklady farmafarmaceutyczne polpharma s.aceutyczne polpharma s.a. - dimethyl fumarate - multiplā skleroze, recidivējoši-pārskaitot - imūnsupresanti - dimethyl fumarate polpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Dimethyl fumarate Teva Ευρωπαϊκή Ένωση - Λετονικά - EMA (European Medicines Agency)

dimethyl fumarate teva

teva gmbh - dimethyl fumarate - multiple sclerosis, relapsing-remitting; multiple sclerosis - imūnsupresanti - 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 Accord Ευρωπαϊκή Ένωση - Λετονικά - EMA (European Medicines Agency)

dimethyl fumarate accord

accord healthcare s.l.u. - dimethyl fumarate - multiple sclerosis, relapsing-remitting; multiple sclerosis - imūnsupresanti - 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 Mylan Ευρωπαϊκή Ένωση - Λετονικά - EMA (European Medicines Agency)

dimethyl fumarate mylan

mylan ireland limited - dimethyl fumarate - multiplā skleroze, recidivējoši-pārskaitot - imūnsupresanti - dimethyl fumarate mylan is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Tecfidera Ευρωπαϊκή Ένωση - Λετονικά - EMA (European Medicines Agency)

tecfidera

biogen netherlands b.v. - dimethyl fumarate - multiplā skleroze - imūnsupresanti - tecfidera is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

Skilarence Ευρωπαϊκή Ένωση - Λετονικά - EMA (European Medicines Agency)

skilarence

almirall s.a - dimethyl fumarate - psoriāze - imūnsupresanti - slimība ir indicēta vidēji smagas vai smagas plaknes psoriāzes ārstēšanai pieaugušajiem, kuriem nepieciešama sistēmiska zāļu terapija.

Vumerity Ευρωπαϊκή Ένωση - Λετονικά - EMA (European Medicines Agency)

vumerity

biogen netherlands b.v. - diroximel fumarate (biib098) - multiplā skleroze, recidivējoši-pārskaitot - imūnsupresanti - vumerity is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis (see section 5. 1 for important information on the populations for which efficacy has been established).