ONDANSETRON KALCEKS 2MG/ML Injekční/infuzní roztok Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

ondansetron kalceks 2mg/ml injekční/infuzní roztok

as kalceks, riga array - 10418 dihydrÁt ondansetron-hydrochloridu - injekční/infuzní roztok - 2mg/ml - ondansetron

ONDANSETRON KABI 2MG/ML Injekční roztok Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

ondansetron kabi 2mg/ml injekční roztok

fresenius kabi deutschland gmbh, bad homburg array - 10418 dihydrÁt ondansetron-hydrochloridu - injekční roztok - 2mg/ml - ondansetron

ONDANSETRON B. BRAUN 2MG/ML Injekční roztok Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

ondansetron b. braun 2mg/ml injekční roztok

b. braun melsungen ag, melsungen array - 10418 dihydrÁt ondansetron-hydrochloridu - injekční roztok - 2mg/ml - ondansetron

ONDANSETRON KABI 0,08MG/ML Infuzní roztok Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

ondansetron kabi 0,08mg/ml infuzní roztok

fresenius kabi deutschland gmbh, bad homburg array - 10418 dihydrÁt ondansetron-hydrochloridu - infuzní roztok - 0,08mg/ml - ondansetron

ONDANSETRON KABI 0,16MG/ML Infuzní roztok Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

ondansetron kabi 0,16mg/ml infuzní roztok

fresenius kabi deutschland gmbh, bad homburg array - 10418 dihydrÁt ondansetron-hydrochloridu - infuzní roztok - 0,16mg/ml - ondansetron

ONDANSETRON TEVA 8MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

ondansetron teva 8mg potahovaná tableta

teva pharmaceuticals cr, s.r.o., praha array - 10418 dihydrÁt ondansetron-hydrochloridu - potahovaná tableta - 8mg - ondansetron

Sitagliptin / Metformin hydrochloride Mylan Evropská unie - čeština - EMA (European Medicines Agency)

sitagliptin / metformin hydrochloride mylan

mylan ireland limited - sitagliptin hydrochloride monohydrate, metformin hydrochloride - diabetes mellitus, typ 2 - léky užívané při diabetu - 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. trojkombinační léčbě) jako doplněk k dietním opatřením a cvičení u pacientů nedostatečně maximální tolerované dávky metforminu a sulfonylmočoviny. 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.

Vildagliptin / Metformin hydrochloride Accord Evropská unie - čeština - EMA (European Medicines Agency)

vildagliptin / metformin hydrochloride accord

accord healthcare s.l.u. - metformin hydrochloride, vildagliptin - diabetes mellitus, typ 2 - léky užívané při diabetu - vildagliptin/metformin hydrochloride accord is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:- in patients who are inadequately controlled with metformin hydrochloride alone. - in patients who are already being treated with the combination of vildagliptin and metformin hydrochloride, as separate tablets. - in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control (see sections 4. 4, 4. 5 a 5. 1 pro dostupné údaje o různých kombinacích).

Sitagliptin / Metformin hydrochloride Sun Evropská unie - čeština - EMA (European Medicines Agency)

sitagliptin / metformin hydrochloride sun

sun pharmaceutical industries europe b.v. - sitagliptin fumarate, metformin hydrochloride - diabetes mellitus, typ 2 - léky užívané při diabetu - 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. trojkombinační léčbě) jako doplněk k dietním opatřením a cvičení u pacientů nedostatečně maximální tolerované dávky metforminu a sulfonylmočoviny. 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.

Sitagliptin / Metformin hydrochloride Accord Evropská unie - čeština - EMA (European Medicines Agency)

sitagliptin / metformin hydrochloride accord

accord healthcare s.l.u. - metformin hydrochloride, sitagliptin hydrochloride monohydrate - diabetes mellitus, typ 2 - léky užívané při diabetu - for adult patients with type 2 diabetes mellitus:it 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. it is indicated in combination with a sulphonylurea (i. trojkombinační léčbě) jako doplněk k dietním opatřením a cvičení u pacientů nedostatečně maximální tolerované dávky metforminu a sulfonylmočoviny. it 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. it 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.