Fenemal 50 mg Norge - norsk - Statens legemiddelverk

fenemal 50 mg

orifarm healthcare a/s - fenobarbital - tablett - 50 mg

Phenoleptil 50 mg Norge - norsk - Statens legemiddelverk

phenoleptil 50 mg

le vet b.v. - fenobarbital - tablett - 50 mg

Phenoleptil 12.5 mg Norge - norsk - Statens legemiddelverk

phenoleptil 12.5 mg

le vet b.v. - fenobarbital - tablett - 12.5 mg

Phenoleptil 25 mg Norge - norsk - Statens legemiddelverk

phenoleptil 25 mg

dechra regulatory b.v. - fenobarbital - tablett - 25 mg

Phenoleptil 100 mg Norge - norsk - Statens legemiddelverk

phenoleptil 100 mg

dechra regulatory b.v. - fenobarbital - tablett - 100 mg

Steripet 250 MBq/ ml Norge - norsk - Statens legemiddelverk

steripet 250 mbq/ ml

ge healthcare b.v. - fludeoksyglukose (18f) - injeksjonsvæske, oppløsning - 250 mbq/ ml

Euthasol vet 400 mg/ ml Norge - norsk - Statens legemiddelverk

euthasol vet 400 mg/ ml

le vet b.v. - pentobarbitalnatrium - injeksjonsvæske, oppløsning - 400 mg/ ml

Exagon vet 400 mg/ ml Norge - norsk - Statens legemiddelverk

exagon vet 400 mg/ ml

vetviva richter gmbh - pentobarbitalnatrium - injeksjonsvæske, oppløsning - 400 mg/ ml

Pentoxin 500 mg/ ml Norge - norsk - Statens legemiddelverk

pentoxin 500 mg/ ml

chanelle pharmaceuticals manufacturing ltd - pentobarbitalnatrium - injeksjonsvæske, oppløsning - 500 mg/ ml

Lynparza Den europeiske union - norsk - 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.