Eiropas Savienība - dāņu - EMA (European Medicines Agency)

amgen europe b.v. - adalimumab - arthritis, psoriatic; spondylitis, ankylosing; crohn disease; colitis, ulcerative; hidradenitis suppurativa; psoriasis; arthritis, rheumatoid - immunosuppressiva - se venligst afsnit 4. 1 i resuméet af produktegenskaber i produktinformationsdokumentet.

Eiropas Savienība - dāņu - EMA (European Medicines Agency)

amgen europe b.v. - darbepoetin alfa - anemia; cancer; kidney failure, chronic - andre præparater antianemic - behandling af symptomatisk anæmi forbundet med kronisk nyresvigt (crf) hos voksne og pædiatriske patienter. behandling af symptomatisk anæmi hos voksne patienter med cancer i ikke-myeloide maligniteter, der modtager kemoterapi.

Eiropas Savienība - dāņu - EMA (European Medicines Agency)

amgen europe b.v. - blinatumomab - forløbercellelimfoblastisk leukæmi-lymfom - antineoplastiske midler - blincyto is indicated as monotherapy for the treatment of adults with cd19 positive relapsed or refractory b precursor acute lymphoblastic leukaemia (all). patients with philadelphia chromosome positive b-precursor all should have failed treatment with at least 2 tyrosine kinase inhibitors (tkis) and have no alternative treatment options. blincyto is indicated as monotherapy for the treatment of adults with philadelphia chromosome negative cd19 positive b-precursor all in first or second complete remission with minimal residual disease (mrd) greater than or equal to 0. blincyto is indicated as monotherapy for the treatment of paediatric patients aged 1 year or older with philadelphia chromosome negative cd19 positive b precursor all which is refractory or in relapse after receiving at least two prior therapies or in relapse after receiving prior allogeneic haematopoietic stem cell transplantation. blincyto is indicated as monotherapy for the treatment of paediatric patients aged 1 year or older with high-risk first relapsed philadelphia chromosome negative cd19 positive b-precursor all as part of the consolidation therapy (see section 4.

Eiropas Savienība - dāņu - EMA (European Medicines Agency)

covis pharma europe b.v. - aclidinium bromide - pulmonal sygdom, kronisk obstruktiv - medicin for obstruktiv sygdomme, - bretaris genuair er indiceret som vedligeholdelsesbronkodilatorbehandling for at lindre symptomer hos voksne patienter med kronisk obstruktiv lungesygdom (copd).

Eiropas Savienība - dāņu - EMA (European Medicines Agency)

covis pharma europe b.v. - formoterol fumarate dihydrate, aclidinium bromide - pulmonal sygdom, kronisk obstruktiv - medicin for obstruktiv sygdomme, - brimica genuair er indiceret som vedligeholdelsesbronkodilatorbehandling for luftstrømningsobstruktion og lindring af symptomer hos voksne patienter med kronisk obstruktiv lungesygdom (copd).

Eiropas Savienība - dāņu - EMA (European Medicines Agency)

covis pharma europe b.v. - aclidinium bromid, formoterol fumarate dihydrat - pulmonal sygdom, kronisk obstruktiv - medicin for obstruktiv sygdomme, - duaklir genuair er indiceret som vedligeholdelsesbronkodilatorbehandling for at lindre symptomer hos voksne patienter med kronisk obstruktiv lungesygdom (copd).

Eiropas Savienība - dāņu - EMA (European Medicines Agency)

covis pharma europe b.v. - aclidinium bromide - pulmonal sygdom, kronisk obstruktiv - medicin for obstruktiv sygdomme, - eklira genuair er indiceret som vedligeholdelsesbronkodilatorbehandling for at lindre symptomer hos voksne patienter med kronisk obstruktiv lungesygdom (copd).

Eiropas Savienība - dāņu - EMA (European Medicines Agency)

amgen europe b.v. - talimogen laherparepvec - melanom - antineoplastiske midler - imlygic er indiceret til behandling af voksne med inoperabel modermærkekræft, regionalt eller fjernt metastatisk (stadie iiib, iiic og ivm1a) med ingen ben, hjerne, lunge eller andre visceral sygdom.

Eiropas Savienība - dāņu - EMA (European Medicines Agency)

amgen europe b.v. - carfilzomib - multipelt myelom - antineoplastiske midler - kyprolis in combination with daratumumab and dexamethasone, with lenalidomide and dexamethasone, or with dexamethasone alone is indicated for the treatment of adult patients with multiple myeloma who have received at least one prior therapy.

Eiropas Savienība - dāņu - EMA (European Medicines Agency)

pfizer europe ma eeig - etanercept - arthritis, psoriatic; spondylitis, ankylosing; psoriasis - immunosuppressiva - reumatoid arthritis;juvenil idiopatisk arthritispsoriatic gigt;aksial spondyloarthritis;plaque psoriasis;pædiatriske plaque psoriasis.