Pamorelin 3,75 mg depotinjektionsvæske, pulver og solvens til suspension Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

pamorelin 3,75 mg depotinjektionsvæske, pulver og solvens til suspension

institut produits synthése (ipsen) ab - triptorelin - depotinjektionsvæske, pulver og solvens til suspension - 3,75 mg

Pamorelin 22,5 mg depotinjektionsvæske, pulver og solvens til suspension Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

pamorelin 22,5 mg depotinjektionsvæske, pulver og solvens til suspension

institut produits synthése (ipsen) ab - triptorelin - depotinjektionsvæske, pulver og solvens til suspension - 22,5 mg

Ypozane Den Europæiske Union - dansk - EMA (European Medicines Agency)

ypozane

virbac s.a. - osateronacetat - urologicals - hunde - behandling af godartet prostatisk hypertrofi (bph) hos hanhunde.

Vaniqa Den Europæiske Union - dansk - EMA (European Medicines Agency)

vaniqa

almirall, s.a. - eflornitin - hirsutisme - andre dermatologiske præparater - behandling af ansigtshirsutisme hos kvinder.

Orgovyx Den Europæiske Union - dansk - EMA (European Medicines Agency)

orgovyx

accord healthcare s.l.u. - relugolix - prostatiske neoplasmer - endokrine terapi - orgovyx is indicated for the treatment of adult patients with advanced hormone-sensitive prostate cancer.

Akeega Den Europæiske Union - dansk - EMA (European Medicines Agency)

akeega

janssen-cilag international n.v. - abiraterone acetate, niraparib tosilate monohydrate - prostatic neoplasmer, kastration-resistent - antineoplastiske midler - treatment of adult patients with prostate cancer.

Orladeyo Den Europæiske Union - dansk - EMA (European Medicines Agency)

orladeyo

biocryst ireland limited - berotralstat dihydrochloride - angioødemer, arvelige - other hematological agents - orladeyo is indicated for routine prevention of recurrent attacks of hereditary angioedema (hae) in adult and adolescent patients aged 12 years and older.

Lynparza Den Europæiske Union - dansk - EMA (European Medicines Agency)

lynparza

astrazeneca ab - olaparib - Æggestokkene neoplasmer - antineoplastiske midler - Æggestokkene cancerlynparza er angivet som monoterapi til:vedligeholdelse behandling af voksne patienter med avanceret (figo faser iii og iv) brca1/2-muterede (germline og/eller somatiske) high-grade epitelial ovariecancer, æggeleder eller primær peritoneal cancer, der er i reaktion (hel eller delvis) efter afslutningen af første linje platin-baseret kemoterapi. 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. patienter bør have, der tidligere er blevet behandlet med en antracyklin og en taxane i (neo)adjuvans eller metastatisk indstilling, medmindre patienter, der ikke var egnet til disse behandlinger (se afsnit 5. patienter med hormon receptor (hr)-positiv brystkræft bør også have udviklet sig på eller efter forudgående endokrine terapi, eller anses uegnet til at endokrine 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.

Ketoconazole HRA Den Europæiske Union - dansk - EMA (European Medicines Agency)

ketoconazole hra

hra pharma rare diseases - ketoconazol - cushing syndrome - antimykotika til systemisk brug - ketoconazol hra er indiceret til behandling af endogent cushings syndrom hos voksne og unge over 12 år.