Sitagliptin / Metformin hydrochloride Sun Euroopan unioni - suomi - EMA (European Medicines Agency)

sitagliptin / metformin hydrochloride sun

sun pharmaceutical industries europe b.v. - sitagliptin fumarate, metformin hydrochloride - diabetes mellitus, tyyppi 2 - diabeetilla käytettävät lääkkeet - for adult patients with type 2 diabetes mellitus:sitagliptin/metformin hydrochloride sun is indicated as an adjunct to diet and exercise to improve glycaemic control in patients inadequately controlled on their maximal tolerated dose of metformin alone or those already being treated with the combination of sitagliptin and metformin. sitagliptin/metformin hydrochloride sun is indicated in combination with a sulphonylurea (i. kolmen lääkkeen yhdistelmähoito) lisänä ruokavalion ja liikunnan ohella potilaille riittävästi hallinnassa heidän maksimaalinen siedetty annos metformiinia ja sulfonyyliureaa. sitagliptin/metformin hydrochloride sun is indicated as triple combination therapy with a peroxisome proliferator-activated receptor gamma (pparγ) agonist (i. , a thiazolidinedione) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a pparγ agonist. sitagliptin/metformin hydrochloride sun is also indicated as add-on to insulin (i. , triple combination therapy) as an adjunct to diet and exercise to improve glycaemic control in patients when stable dose of insulin and metformin alone do not provide adequate glycaemic control.

Sunitinib Accord Euroopan unioni - suomi - EMA (European Medicines Agency)

sunitinib accord

accord healthcare s.l.u. - sunitinibi - gastrointestinal stromal tumors; carcinoma, renal cell; neuroendocrine tumors - antineoplastiset aineet - gastrointestinal stromal tumour (gist)sunitinib accord is indicated for the treatment of unresectable and/or metastatic malignant gastrointestinal stromal tumour (gist) in adults after failure of imatinib treatment due to resistance or intolerance. metastatic renal cell carcinoma (mrcc)sunitinib accord is indicated for the treatment of advanced/metastatic renal cell carcinoma (mrcc) in adults. pancreatic neuroendocrine tumours (pnet)sunitinib accord is indicated for the treatment of unresectable or metastatic, well-differentiated pancreatic neuroendocrine tumours (pnet) with disease progression in adults.

Sunitinib Ratiopharm 12.5 mg kapseli, kova Suomi - suomi - Fimea (Suomen lääkevirasto)

sunitinib ratiopharm 12.5 mg kapseli, kova

ratiopharm gmbh - sunitinib - kapseli, kova - 12.5 mg - sunitinibi

Sunitinib Ratiopharm 25 mg kapseli, kova Suomi - suomi - Fimea (Suomen lääkevirasto)

sunitinib ratiopharm 25 mg kapseli, kova

ratiopharm gmbh - sunitinib - kapseli, kova - 25 mg - sunitinibi

Sunitinib Ratiopharm 37.5 mg kapseli, kova Suomi - suomi - Fimea (Suomen lääkevirasto)

sunitinib ratiopharm 37.5 mg kapseli, kova

ratiopharm gmbh - sunitinib - kapseli, kova - 37.5 mg - sunitinibi

Sunitinib Ratiopharm 50 mg kapseli, kova Suomi - suomi - Fimea (Suomen lääkevirasto)

sunitinib ratiopharm 50 mg kapseli, kova

ratiopharm gmbh - sunitinib - kapseli, kova - 50 mg - sunitinibi

Sunitinib Sandoz 12.5 mg kapseli, kova Suomi - suomi - Fimea (Suomen lääkevirasto)

sunitinib sandoz 12.5 mg kapseli, kova

sandoz a/s - sunitinib - kapseli, kova - 12.5 mg - sunitinibi

Sunitinib Sandoz 25 mg kapseli, kova Suomi - suomi - Fimea (Suomen lääkevirasto)

sunitinib sandoz 25 mg kapseli, kova

sandoz a/s - sunitinib - kapseli, kova - 25 mg - sunitinibi

Sunitinib Sandoz 37.5 mg kapseli, kova Suomi - suomi - Fimea (Suomen lääkevirasto)

sunitinib sandoz 37.5 mg kapseli, kova

sandoz a/s - sunitinib - kapseli, kova - 37.5 mg - sunitinibi

Sunitinib Sandoz 50 mg kapseli, kova Suomi - suomi - Fimea (Suomen lääkevirasto)

sunitinib sandoz 50 mg kapseli, kova

sandoz a/s - sunitinib - kapseli, kova - 50 mg - sunitinibi