Lynparza Europese Unie - Noors - EMA (European Medicines Agency)

lynparza

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.

Duodopa 20 mg/ ml / 5 mg/ ml Noorwegen - Noors - Statens legemiddelverk

duodopa 20 mg/ ml / 5 mg/ ml

abbvie as - levodopa / karbidopamonohydrat - intestinalgel - 20 mg/ ml / 5 mg/ ml

Tegretol 200 mg Noorwegen - Noors - Statens legemiddelverk

tegretol 200 mg

novartis norge (2) - karbamazepin - tablett - 200 mg

Tegretol 20 mg/ ml Noorwegen - Noors - Statens legemiddelverk

tegretol 20 mg/ ml

novartis norge (2) - karbamazepin - mikstur, suspensjon - 20 mg/ ml

Tegretol 100 mg Noorwegen - Noors - Statens legemiddelverk

tegretol 100 mg

novartis norge (2) - karbamazepin - tablett - 100 mg

Tegretol Retard 400 mg Noorwegen - Noors - Statens legemiddelverk

tegretol retard 400 mg

novartis norge (2) - karbamazepin - depottablett - 400 mg

Tegretol Retard 200 mg Noorwegen - Noors - Statens legemiddelverk

tegretol retard 200 mg

novartis norge (2) - karbamazepin - depottablett - 200 mg

Deferasirox Mylan Europese Unie - Noors - EMA (European Medicines Agency)

deferasirox mylan

mylan pharmaceuticals limited - deferasiroks - iron overload; beta-thalassemia - strykejern chelatdannere - deferasirox mylan er angitt forthe behandling av kronisk jern overbelastning på grunn av hyppige blodoverføringer (≥7 ml/kg/måned pakket røde blodlegemer) hos pasienter med beta thalassaemia store alderen 6 år og olderthe behandling av kronisk jern overbelastning på grunn av blodoverføringer når deferoxamine behandling er kontraindisert eller utilstrekkelig i følgende pasientgrupper:i paediatric pasienter med beta thalassaemia store med jern overbelastning på grunn av hyppige blodoverføringer (≥7 ml/kg/måned pakket røde blodceller) i alderen 2 til 5 år,i voksen og paediatric pasienter med beta thalassaemia store med jern overbelastning på grunn av sjeldne blodoverføringer (.

Tabrecta Europese Unie - Noors - EMA (European Medicines Agency)

tabrecta

novartis europharm limited  - capmatinib dihydrochloride monohydrate - karsinom, ikke-småcellet lunge - antineoplastiske midler - tabrecta as monotherapy is indicated for the treatment of adult patients with advanced non small cell lung cancer (nsclc) harbouring alterations leading to mesenchymal epithelial transition factor gene exon 14 (metex14) skipping, who require systemic therapy following prior treatment with immunotherapy and/or platinum based chemotherapy.

Produodopa 240 mg/ ml / 12 mg/ ml Noorwegen - Noors - Statens legemiddelverk

produodopa 240 mg/ ml / 12 mg/ ml

abbvie as - foslevodopa / foskarbidopa - infusjonsvæske, oppløsning - 240 mg/ ml / 12 mg/ ml