Európska únia - fínčina - EMA (European Medicines Agency)

novartis europharm limited  - onasemnogene abeparvovec - lihassärky, spinaali - muut lääkkeet liikuntaelinten sairauksien häiriöihin - zolgensma on tarkoitettu hoitoon:potilaat, joilla 5q selkärangan lihasten surkastumista (sma), jossa on bi-alleeliset mutaatio smn1-geenin ja kliininen diagnoosi sma tyyppi 1, orpatients kanssa 5q sma, jossa on bi-alleeliset mutaatio smn1-geenin ja jopa 3 kopiota smn2-geeni.

Európska únia - fínčina - EMA (European Medicines Agency)

orchard therapeutics (netherlands) bv - atidarsagene autotemcel - leukodystrophy, metachromatic - muut hermoston huumeet - libmeldy is indicated for the treatment of metachromatic leukodystrophy (mld) characterized by biallelic mutations in the arysulfatase a (arsa) gene leading to a reduction of the arsa enzymatic activity:in children with late infantile or early juvenile forms, without clinical manifestations of the disease,in children with the early juvenile form, with early clinical manifestations of the disease, who still  have the ability to walk independently and before the onset of cognitive decline.

Fínsko - fínčina - Fimea (Suomen lääkevirasto)

vetpharma animal health, s.l. - isoflurane - inhalaatiohöyry, neste - 1000 mg/g - isofluraani

Európska únia - fínčina - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - idecabtagene vicleucel - multiple myeloma; neoplasms; cancer; neoplasms, plasma cell; hemostatic disorders; vascular diseases; cardiovascular diseases; paraproteinemias; blood protein disorders; hematologic diseases; hemic and lymphatic diseases; hemorrhagic disorders; infectious mononucleosis; lymphoproliferative disorders; immunoproliferative disorders; immune system diseases - antineoplastiset aineet - abecma is indicated for the treatment of adult patients with relapsed and refractory multiple myeloma who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor and an anti cd38 antibody and have demonstrated disease progression on the last therapy.

Európska únia - fínčina - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - cd19-directed genetically modified autologous cell-based product consisting of purified cd8+ t-cells (cd8+ cells), cd19-directed genetically modified autologous cell-based product consisting of purified cd4+ t cells (cd4+ cells) - lymphoma, large b-cell, diffuse; lymphoma, follicular; mediastinal neoplasms - antineoplastiset aineet - breyanzi is indicated for the treatment of adult patients with diffuse large b-cell lymphoma (dlbcl), high grade b-cell lymphoma (hgbcl), primary mediastinal large b-cell lymphoma (pmbcl) and follicular lymphoma grade 3b (fl3b), who relapsed within 12 months from completion of, or are refractory to, first-line chemoimmunotherapy.

Európska únia - fínčina - EMA (European Medicines Agency)

ptc therapeutics international limited - eladocagene exuparvovec - aminohappoaineenvaihdunta, synnynnäiset virheet - enzymes, other alimentary tract and metabolism products - upstaza is indicated for the treatment of patients aged 18 months and older with a clinical, molecular, and genetically confirmed diagnosis of aromatic l amino acid decarboxylase (aadc) deficiency with a severe phenotype (see section 5.

Európska únia - fínčina - EMA (European Medicines Agency)

extrovis eu ltd. - sugammadex sodium - neuromuskulaarinen estäminen - kaikki muut terapeuttiset tuotteet - reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Európska únia - fínčina - EMA (European Medicines Agency)

extrovis eu ltd. - lakosamidi - epilepsia - epilepsialääkkeet, - lacosamide adroiq is indicated as monotherapy in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 2 years of age with epilepsy. lacosamide adroiq is indicated as adjunctive therapyin the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 2 years of age with epilepsy. in the treatment of primary generalised tonic-clonic seizures in adults, adolescents and children from 4 years of age with idiopathic generalised epilepsy.

Fínsko - fínčina - Fimea (Suomen lääkevirasto)

mip pharma gmbh - cefotaxime sodium - injektio-/infuusiokuiva-aine liuosta varten - 1 g - kefotaksiimi

Fínsko - fínčina - Fimea (Suomen lääkevirasto)

mip pharma gmbh - cefotaxime sodium - injektio-/infuusiokuiva-aine liuosta varten - 2 g - kefotaksiimi