Նորվեգիա - Նորվեգերեն - Statens legemiddelverk

orifarm as - dabigatraneteksilat - kapsel, hard - 150 mg

Եվրոպական Միություն - Նորվեգերեն - EMA (European Medicines Agency)

astrazeneca ab - olaparib - ovarie neoplasmer - antineoplastiske midler - ovarian cancerlynparza er indisert som monoterapi for:vedlikehold behandling av voksne pasienter med avansert (figo stadier iii og iv) brca1/2-muterte (germline og/eller somatiske) high-grade epithelial ovarian, fallopian tube eller primære peritoneal kreft som er i respons (hel eller delvis) etter gjennomføring av første-linje platinum-basert kjemoterapi. maintenance treatment of adult patients with platinum sensitive relapsed high grade epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) to platinum based chemotherapy. lynparza in combination with bevacizumab is indicated for the:maintenance treatment of adult patients with advanced (figo stages iii and iv) high-grade epithelial ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy in combination with bevacizumab and whose cancer is associated with homologous recombination deficiency (hrd) positive status defined by either a brca1/2 mutation and/or genomic instability (see section 5. breast cancerlynparza is indicated as:monotherapy or in combination with endocrine therapy for the adjuvant treatment of adult patients with germline brca1/2-mutations who have her2-negative, high risk early breast cancer previously treated with neoadjuvant or adjuvant chemotherapy (see sections 4. 2 og 5. monotherapy for the treatment of adult patients with germline brca1/2-mutations, who have her2 negative locally advanced or metastatic breast cancer. pasienter bør ha tidligere blitt behandlet med en anthracycline og en taxane i (neo)adjuvant eller metastatisk innstillingen med mindre pasienter ikke var egnet for disse behandlingene (se punkt 5.. pasienter med hormon-reseptor (hr)-positiv brystkreft bør også ha utviklet seg på eller etter forutgående endokrin terapi, eller anses som uegnet for endokrin terapi. adenocarcinoma of the pancreaslynparza is indicated as:monotherapy for the maintenance treatment of adult patients with germline brca1/2-mutations who have metastatic adenocarcinoma of the pancreas and have not progressed after a minimum of 16 weeks of platinum treatment within a first-line chemotherapy regimen. prostate cancerlynparza is indicated as:monotherapy for the treatment of adult patients with metastatic castration-resistant prostate cancer (mcrpc) and brca1/2-mutations (germline and/or somatic) who have progressed following prior therapy that included a new hormonal agent. in combination with abiraterone and prednisone or prednisolone for the treatment of adult patients with mcrpc in whom chemotherapy is not clinically indicated (see section 5.

Եվրոպական Միություն - Նորվեգերեն - EMA (European Medicines Agency)

pfizer europe ma eeig - somatrogon - growth and development - hypofysen og hypothalamus hormoner og analoger - indicated for the long-term treatment of paediatric patients with growth disturbance due to insufficient secretion of growth hormone.

Եվրոպական Միություն - Նորվեգերեն - EMA (European Medicines Agency)

alnylam netherlands b.v. - vutrisiran sodium - amyloid neuropathies, familial - andre nervesystemet narkotika - treatment of hereditary transthyretin-mediated amyloidosis (hattr amyloidosis) in adult patients with stage 1 or stage 2 polyneuropathy.

Եվրոպական Միություն - Նորվեգերեն - EMA (European Medicines Agency)

eli lilly nederland b.v. - duloksetin - diabetiske neuropatier - psychoanaleptics, - behandling av diabetisk perifer neuropatisk smerte. ariclaim er indisert hos voksne.

Եվրոպական Միություն - Նորվեգերեն - EMA (European Medicines Agency)

chiesi farmaceutici s.p.a - idebenone - optisk atrofi, arvelig, leber - andre psychostimulants og nootropics, psychoanaleptics, - raxone er indisert for behandling av synshemming hos ungdoms- og voksne pasienter med leber's hereditary optic neuropathy (lhon).

Եվրոպական Միություն - Նորվեգերեն - EMA (European Medicines Agency)

les laboratoires servier - ivosidenib - leukemia, myeloid, acute; cholangiocarcinoma - antineoplastiske midler - tibsovo in combination with azacitidine is indicated for the treatment of adult patients with newly diagnosed acute myeloid leukaemia (aml) with an isocitrate dehydrogenase-1 (idh1) r132 mutation who are not eligible to receive standard induction chemotherapy (see section 5. tibsovo monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic cholangiocarcinoma with an idh1 r132 mutation who were previously treated by at least one prior line of systemic therapy.

Եվրոպական Միություն - Նորվեգերեն - EMA (European Medicines Agency)

roche registration gmbh  - risdiplam - muskelatrofi, spinal - andre legemidler for forstyrrelser i muskel-skjelettsystemet - evrysdi is indicated for the treatment of 5q spinal muscular atrophy (sma) in patients with a clinical diagnosis of sma type 1, type 2 or type 3 or with one to four smn2 copies.

Եվրոպական Միություն - Նորվեգերեն - EMA (European Medicines Agency)

virbac s.a. - clomipramine hydrochloride - psychoanaleptics - hunder - as an aid in the treatment of separation related disorders in dogs manifested by destruction and inappropriate elimination (defecation and urination) and only in combination with behavioural modification techniques.

Եվրոպական Միություն - Նորվեգերեն - EMA (European Medicines Agency)

mylan ireland limited - sugammadex sodium - neuromuskulær blokkade - alle andre terapeutiske produkter - 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.