Lipocomb Neo 20 mg/10 mg Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

lipocomb neo 20 mg/10 mg

egis pharmaceuticals plc, maďarsko - rosuvastatín a ezetimib - 31 - hypolipidaemica

Lipocomb Neo 10 mg/10 mg Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

lipocomb neo 10 mg/10 mg

egis pharmaceuticals plc, maďarsko - rosuvastatín a ezetimib - 31 - hypolipidaemica

Lipocomb 40 mg/10 mg Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

lipocomb 40 mg/10 mg

egis pharmaceuticals plc, maďarsko - rosuvastatín a ezetimib - 31 - hypolipidaemica

Lipocomb 20 mg/10 mg Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

lipocomb 20 mg/10 mg

egis pharmaceuticals plc, maďarsko - rosuvastatín a ezetimib - 31 - hypolipidaemica

Lipocomb 10 mg/10 mg Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

lipocomb 10 mg/10 mg

egis pharmaceuticals plc, maďarsko - rosuvastatín a ezetimib - 31 - hypolipidaemica

Eucreas Európska únia - slovenčina - EMA (European Medicines Agency)

eucreas

novartis europharm limited - vildagliptin, hydrochlorid metformín - diabetes mellitus, typ 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - eucreas 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.

Icandra (previously Vildagliptin / metformin hydrochloride Novartis) Európska únia - slovenčina - EMA (European Medicines Agency)

icandra (previously vildagliptin / metformin hydrochloride novartis)

novartis europharm limited - vildagliptin, hydrochlorid metformín - diabetes mellitus, typ 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - icandra 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 pre dostupné údaje o rôznych kombináciách).

Segluromet Európska únia - slovenčina - EMA (European Medicines Agency)

segluromet

merck sharp & dohme b.v. - ertugliflozin l-pyroglutamic acid, metformin hydrochloride - diabetes mellitus, typ 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.

Sitagliptin/Metformin Krka 50 mg/850 mg filmom obalené tablety Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

sitagliptin/metformin krka 50 mg/850 mg filmom obalené tablety

krka, d.d., novo mesto, slovinsko - metformín a sitagliptín - 18 - antidiabetica (vrÁtane inzulÍnu)

Teysuno Európska únia - slovenčina - EMA (European Medicines Agency)

teysuno

nordic group b.v. - tegafur, gimeracil, oteracil - neoplazmy žalúdka - antineoplastické činidlá - teysuno is indicated in adults:- for the treatment of advanced gastric cancer when given in combination with cisplatin (see section 5. - as monotherapy or in combination with oxaliplatin or irinotecan, with or without bevacizumab, for the treatment of patients with metastatic colorectal cancer for whom it is not possible to continue treatment with another fluoropyrimidine due to hand-foot syndrome or cardiovascular toxicity that developed in the adjuvant or metastatic setting.