Skilarence Europese Unie - Nederlands - EMA (European Medicines Agency)

skilarence

almirall s.a - dimethylfumaraat - psoriasis - immunosuppressiva - skilarence is geïndiceerd voor de behandeling van matige tot ernstige plaque psoriasis bij volwassenen die systemische medicinale therapie nodig hebben.

Tecfidera Europese Unie - Nederlands - EMA (European Medicines Agency)

tecfidera

biogen netherlands b.v. - dimethylfumaraat - multiple sclerose - immunosuppressiva - tecfidera is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

Lenalidomide Mylan Europese Unie - Nederlands - EMA (European Medicines Agency)

lenalidomide mylan

mylan ireland limited - lenalidomide - multiple myeloma - immunosuppressiva - multiple myelomalenalidomide mylan as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide mylan as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone is indicated for the treatment of adult patients with previously untreated multiple myeloma who are not eligible for transplant. lenalidomide mylan in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. follicular lymphomalenalidomide mylan in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1-3a).

Vumerity Europese Unie - Nederlands - EMA (European Medicines Agency)

vumerity

biogen netherlands b.v. - diroximel fumarate (biib098) - multiple sclerose, relapsing-remitting - immunosuppressiva - 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).

Dimethyl fumarate Mylan Europese Unie - Nederlands - EMA (European Medicines Agency)

dimethyl fumarate mylan

mylan ireland limited - dimethylfumaraat - multiple sclerose, relapsing-remitting - immunosuppressiva - dimethyl fumarate mylan is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Dimethyl fumarate Polpharma Europese Unie - Nederlands - EMA (European Medicines Agency)

dimethyl fumarate polpharma

zaklady farmafarmaceutyczne polpharma s.aceutyczne polpharma s.a. - dimethylfumaraat - multiple sclerose, relapsing-remitting - immunosuppressiva - dimethyl fumarate polpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Dimethyl fumarate Neuraxpharm Europese Unie - Nederlands - EMA (European Medicines Agency)

dimethyl fumarate neuraxpharm

laboratorios lesvi s.l. - dimethylfumaraat - multiple sclerose, relapsing-remitting - immunosuppressiva - dimethyl fumarate neuraxpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Dimtruzic 120 mg harde maagsapresist. caps. België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

dimtruzic 120 mg harde maagsapresist. caps.

sandoz sa-nv - dimethylfumaraat 120 mg - maagsapresistente capsule, hard - dimethyl fumarate

Dimtruzic 240 mg harde maagsapresist. caps. België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

dimtruzic 240 mg harde maagsapresist. caps.

sandoz sa-nv - dimethylfumaraat 240 mg - maagsapresistente capsule, hard - dimethyl fumarate

Dimethyl fumarate Teva Europese Unie - Nederlands - EMA (European Medicines Agency)

dimethyl fumarate teva

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