Lynparza Europeiska unionen - svenska - EMA (European Medicines Agency)

lynparza

astrazeneca ab - olaparib - Äggstockar neoplasmer - antineoplastiska medel - Äggstockscancer cancerlynparza är indicerat som monoterapi för:underhåll behandling av vuxna patienter med avancerad (figo stadierna iii och iv) brca1/2-muterad (könsceller och/eller somatisk) hög-kvalitet epitelial äggstockscancer, äggledare eller primär peritoneal cancer, som är ett svar på (helt eller delvis) efter genomförandet av den första linjens platinum-baserad 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 och 5. monotherapy for the treatment of adult patients with germline brca1/2-mutations, who have her2 negative locally advanced or metastatic breast cancer. patienter bör ha tidigare behandlats med en anthracycline och en taxane i (neo)adjuvant eller metastaserande inställningen om patienter som inte var lämpliga för dessa behandlingar (se avsnitt 5. patienter med hormon receptor (hr)-positiv bröstcancer bör också ha kommit på eller efter föregående endokrin terapi, eller anses vara olämpliga för 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.

Plenadren Europeiska unionen - svenska - EMA (European Medicines Agency)

plenadren

takeda pharmaceuticals international ag ireland branch - hydrokortison - bihålsinsufficiens - kortikosteroider för systemisk användning - behandling av binjurinsufficiens hos vuxna.

Onglyza Europeiska unionen - svenska - EMA (European Medicines Agency)

onglyza

astrazeneca ab - saxagliptin - diabetes mellitus, typ 2 - läkemedel som används vid diabetes - add-on combination therapyonglyza is indicated in adult patients aged 18 years and older with type-2 diabetes mellitus to improve glycaemic control:as monotherapy:in patients inadequately controlled by diet and exercise alone and for whom metformin is inappropriate due to contraindications or intolerance;as dual oral therapy:in combination with metformin, when metformin alone, with diet and exercise, does not provide adequate glycaemic control;in combination with a sulphonylurea, when the sulphonylurea alone, with diet and exercise, does not provide adequate glycaemic control in patients for whom use of metformin is considered inappropriate;in combination with a thiazolidinedione, when the thiazolidinedione alone with diet and exercise, does not provide adequate glycaemic control in patients for whom use of a thiazolidinedione is considered appropriate;as triple oral therapy:in combination with metformin plus a sulphonylurea when this regimen alone, with diet and exercise, does not provide adequate glycaemic control;as combination therapy with insulin (with or without metformin), when this regimen alone, with diet and exercise, does not provide adequate glycaemic control.

Fosrenol 500 mg Tuggtablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

fosrenol 500 mg tuggtablett

orifarm ab - lantan(iii)karbonattetrahydrat - tuggtablett - 500 mg - dextrat, hydratiserat hjälpämne; lantan(iii)karbonattetrahydrat 954 mg aktiv substans - lantankarbonat

Elvanse Vuxen 30 mg Kapsel, hård Sverige - svenska - Läkemedelsverket (Medical Products Agency)

elvanse vuxen 30 mg kapsel, hård

takeda pharmaceuticals international ag ireland branch - lisdexamfetamindimesilat - kapsel, hård - 30 mg - propylenglykol hjälpämne; lisdexamfetamindimesilat 30 mg aktiv substans - lisdexamfetamin

Elvanse Vuxen 50 mg Kapsel, hård Sverige - svenska - Läkemedelsverket (Medical Products Agency)

elvanse vuxen 50 mg kapsel, hård

takeda pharmaceuticals international ag ireland branch - lisdexamfetamindimesilat - kapsel, hård - 50 mg - propylenglykol hjälpämne; lisdexamfetamindimesilat 50 mg aktiv substans - lisdexamfetamin

Elvanse Vuxen 70 mg Kapsel, hård Sverige - svenska - Läkemedelsverket (Medical Products Agency)

elvanse vuxen 70 mg kapsel, hård

takeda pharmaceuticals international ag ireland branch - lisdexamfetamindimesilat - kapsel, hård - 70 mg - lisdexamfetamindimesilat 70 mg aktiv substans; propylenglykol hjälpämne - lisdexamfetamin

Ibuprofen Bril 200 mg Filmdragerad tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

ibuprofen bril 200 mg filmdragerad tablett

brillpharma (ireland) limited - ibuprofen - filmdragerad tablett - 200 mg - ibuprofen 200 mg aktiv substans; laktosmonohydrat hjälpämne; natriumlaurilsulfat hjälpämne - ibuprofen

Medarin Veckotablett 70 mg Tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

medarin veckotablett 70 mg tablett

teva b.v. - natriumalendronattrihydrat - tablett - 70 mg - laktosmonohydrat hjälpämne; natriumalendronattrihydrat 91,36 mg aktiv substans - alendronsyra

Alendroarrow Veckotablett 70 mg Tablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

alendroarrow veckotablett 70 mg tablett

teva b.v. - natriumalendronattrihydrat - tablett - 70 mg - natriumalendronattrihydrat 91,36 mg aktiv substans; laktosmonohydrat hjälpämne - alendronsyra