Rybelsus Europäische Union - Tschechisch - EMA (European Medicines Agency)

rybelsus

novo nordisk a/s - semaglutid - diabetes mellitus, typ 2 - léky užívané při diabetu - rybelsus je indikován k léčbě dospělých pacientů s nedostatečně kontrolovaným diabetes mellitus 2. typu ke zlepšení kontroly glykémie jako doplněk k dietním opatřením a exerciseas monoterapie při léčbě metforminem je považováno za nevhodné v důsledku intolerance nebo contraindicationsin kombinaci s jinými léčivými přípravky k léčbě diabetu. pro výsledky studií s ohledem na kombinace, účinky na kontrolu glykémie a kardiovaskulárních příhod, a populace studoval, viz bod 4. 4, 4. 5 a 5.

Sitagliptin SUN Europäische Union - Tschechisch - EMA (European Medicines Agency)

sitagliptin sun

sun pharmaceutical industries europe b.v. - sitagliptin fumarate - diabetes mellitus, typ 2 - léky užívané při diabetu - for adult patients with type 2 diabetes mellitus, sitagliptin sun is indicated 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 diet and exercise plus metformin alone do not provide adequate glycaemic control. - a sulphonylurea when diet and exercise plus maximal tolerated dose of a sulphonylurea alone do not provide adequate glycaemic control and when metformin is inappropriate due to contraindications or intolerance. - a peroxisome proliferator-activated receptor gamma (pparγ) agonist (i. a thiazolidinedione) when use of a pparγ agonist is appropriate and when diet and exercise plus the pparγ agonist alone do not provide adequate glycaemic control. as triple oral therapy in combination with:- a sulphonylurea and metformin when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control. - a pparγ agonist and metformin when use of a pparγ agonist is appropriate and when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control. sitagliptin sun is also indicated as add-on to insulin (with or without metformin) when diet and exercise plus stable dose of insulin do not provide adequate glycaemic control.

Mounjaro Europäische Union - Tschechisch - EMA (European Medicines Agency)

mounjaro

eli lilly nederland b.v. - tirzepatide - diabetes mellitus, typ 2 - léky užívané při diabetu - mounjaro is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise- as monotherapy when metformin is considered inappropriate due to intolerance or contraindications- in addition to other medicinal products for the treatment of diabetes. for study results with respect to combinations, effects on glycaemic control and the populations studied, see sections 4. 4, 4. 5 a 5.

VILDAGLIPTIN/METFORMIN SANDOZ 50MG/1000MG Potahovaná tableta Tschechische Republik - Tschechisch - SUKL (Státní ústav pro kontrolu léčiv)

vildagliptin/metformin sandoz 50mg/1000mg potahovaná tableta

sandoz s.r.o., praha array - 17128 vildagliptin; 2418 metformin-hydrochlorid - potahovaná tableta - 50mg/1000mg - metformin a vildagliptin

VILDAGLIPTIN/METFORMIN SANDOZ 50MG/850MG Potahovaná tableta Tschechische Republik - Tschechisch - SUKL (Státní ústav pro kontrolu léčiv)

vildagliptin/metformin sandoz 50mg/850mg potahovaná tableta

sandoz s.r.o., praha array - 17128 vildagliptin; 2418 metformin-hydrochlorid - potahovaná tableta - 50mg/850mg - metformin a vildagliptin

METFORMIN SANDOZ 500MG Potahovaná tableta Tschechische Republik - Tschechisch - SUKL (Státní ústav pro kontrolu léčiv)

metformin sandoz 500mg potahovaná tableta

sandoz s.r.o., praha array - 2418 metformin-hydrochlorid - potahovaná tableta - 500mg - metformin

METFORMIN SANDOZ 850MG Potahovaná tableta Tschechische Republik - Tschechisch - SUKL (Státní ústav pro kontrolu léčiv)

metformin sandoz 850mg potahovaná tableta

sandoz s.r.o., praha array - 2418 metformin-hydrochlorid - potahovaná tableta - 850mg - metformin

Memantine Mylan Europäische Union - Tschechisch - EMA (European Medicines Agency)

memantine mylan

mylan pharmaceuticals limited - memantin hydrochlorid - alzheimerova choroba - other anti-dementia drugs, psychoanaleptics, - léčba pacientů se středně závažnou až závažnou alzheimerovou chorobou.

SITAGLIPTIN/METFORMIN TEVA 50MG/1000MG Potahovaná tableta Tschechische Republik - Tschechisch - SUKL (Státní ústav pro kontrolu léčiv)

sitagliptin/metformin teva 50mg/1000mg potahovaná tableta

teva pharmaceuticals cr, s.r.o., praha array - 41 monohydrÁt sitagliptin-hydrochloridu; 2418 metformin-hydrochlorid - potahovaná tableta - 50mg/1000mg - metformin a sitagliptin

SITAGLIPTIN/METFORMIN TEVA 50MG/850MG Potahovaná tableta Tschechische Republik - Tschechisch - SUKL (Státní ústav pro kontrolu léčiv)

sitagliptin/metformin teva 50mg/850mg potahovaná tableta

teva pharmaceuticals cr, s.r.o., praha array - 41 monohydrÁt sitagliptin-hydrochloridu; 2418 metformin-hydrochlorid - potahovaná tableta - 50mg/850mg - metformin a sitagliptin