Finnország - finn - Fimea (Suomen lääkevirasto)

orion corporation - hydroxyzini hydrochloridum - tabletti, kalvopäällysteinen - 25 mg - hydroksitsiini

Finnország - finn - Fimea (Suomen lääkevirasto)

accord healthcare b.v. - metformin hydrochloride - depottabletti - 500 mg - metformiini

Európai Unió - finn - EMA (European Medicines Agency)

merck sharp & dohme b.v. - ertugliflozin l-pyroglutamic acid, metformin hydrochloride - diabetes mellitus, tyyppi 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - segluromet is indicated in adults aged 18 years and older with type 2 diabetes mellitus as an adjunct to diet and exercise to improve glycaemic control:in patients not adequately controlled on their maximally tolerated dose of metformin alonein patients on their maximally tolerated doses of metformin in addition to other medicinal products for the treatment of diabetesin patients already being treated with the combination of ertugliflozin and metformin as separate tablets.

Finnország - finn - Fimea (Suomen lääkevirasto)

teva b.v. - metformin hydrochloride, vildagliptin - tabletti, kalvopäällysteinen - 50 mg / 850 mg - metformiini ja vildagliptiini

Finnország - finn - Fimea (Suomen lääkevirasto)

teva b.v. - metformin hydrochloride, vildagliptin - tabletti, kalvopäällysteinen - 50 mg / 1000 mg - metformiini ja vildagliptiini

Finnország - finn - Fimea (Suomen lääkevirasto)

sandoz a/s - metformin hydrochloride, sitagliptin hydrochloride monohydrate - tabletti, kalvopäällysteinen - 50 mg / 850 mg - metformiini ja sitagliptiini

Finnország - finn - Fimea (Suomen lääkevirasto)

sandoz a/s - metformin hydrochloride, sitagliptin hydrochloride monohydrate - tabletti, kalvopäällysteinen - 50 mg / 1000 mg - metformiini ja sitagliptiini

Finnország - finn - Fimea (Suomen lääkevirasto)

krka, d.d., novo mesto - metformin hydrochloride, sitagliptin - tabletti, kalvopäällysteinen - 50 mg / 850 mg - metformiini ja sitagliptiini

Finnország - finn - Fimea (Suomen lääkevirasto)

krka, d.d., novo mesto - metformin hydrochloride, sitagliptin - tabletti, kalvopäällysteinen - 50 mg / 1000 mg - metformiini ja sitagliptiini

Európai Unió - finn - EMA (European Medicines Agency)

mylan ireland limited - sitagliptin hydrochloride monohydrate, metformin hydrochloride - diabetes mellitus, tyyppi 2 - diabeetilla käytettävät lääkkeet - for adult patients with type 2 diabetes mellitus:sitagliptin/metformin hydrochloride mylan 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 mylan 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 mylan is indicated as triple combination therapy with a peroxisome proliferator-activated receptor gamma (pparg) agonist (i. , a thiazolidinedione) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a pparg agonist. sitagliptin/metformin hydrochloride mylan 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.