Sitagliptin / Metformin hydrochloride Mylan Europeiska unionen - svenska - EMA (European Medicines Agency)

sitagliptin / metformin hydrochloride mylan

mylan ireland limited - sitagliptin hydrochloride monohydrate, metformin hydrochloride - diabetes mellitus, typ 2 - läkemedel som används vid diabetes - 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. - , trippel kombinationsterapi) som ett komplement till kost och motion hos patienter bristfälligt kontrollerad på deras maximal tolererad dos av metformin och en sulphonylurea. 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.

Segluromet Europeiska unionen - svenska - 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.

Pramipexol STADA 0,26 mg Depottablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

pramipexol stada 0,26 mg depottablett

stada arzneimittel ag - pramipexoldihydrokloridmonohydrat - depottablett - 0,26 mg - pramipexoldihydrokloridmonohydrat 0,375 mg aktiv substans

Pramipexol STADA 2,10 mg Depottablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

pramipexol stada 2,10 mg depottablett

stada arzneimittel ag - pramipexoldihydrokloridmonohydrat - depottablett - 2,10 mg - pramipexoldihydrokloridmonohydrat 3 mg aktiv substans

Pramipexol STADA 2,62 mg Depottablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

pramipexol stada 2,62 mg depottablett

stada arzneimittel ag - pramipexoldihydrokloridmonohydrat - depottablett - 2,62 mg - pramipexoldihydrokloridmonohydrat 3,75 mg aktiv substans

Pramipexol STADA 0,52 mg Depottablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

pramipexol stada 0,52 mg depottablett

stada arzneimittel ag - pramipexoldihydrokloridmonohydrat - depottablett - 0,52 mg - pramipexoldihydrokloridmonohydrat 0,75 mg aktiv substans

Pramipexol STADA 1,05 mg Depottablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

pramipexol stada 1,05 mg depottablett

stada arzneimittel ag - pramipexoldihydrokloridmonohydrat - depottablett - 1,05 mg - pramipexoldihydrokloridmonohydrat 1,5 mg aktiv substans

Pramipexol STADA 1,57 mg Depottablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

pramipexol stada 1,57 mg depottablett

stada arzneimittel ag - pramipexoldihydrokloridmonohydrat - depottablett - 1,57 mg - pramipexoldihydrokloridmonohydrat 2,25 mg aktiv substans

Pramipexol STADA 3,15 mg Depottablett Sverige - svenska - Läkemedelsverket (Medical Products Agency)

pramipexol stada 3,15 mg depottablett

stada arzneimittel ag - pramipexoldihydrokloridmonohydrat - depottablett - 3,15 mg - pramipexoldihydrokloridmonohydrat 4,5 mg aktiv substans

Icandra (previously Vildagliptin / metformin hydrochloride Novartis) Europeiska unionen - svenska - EMA (European Medicines Agency)

icandra (previously vildagliptin / metformin hydrochloride novartis)

novartis europharm limited - vildagliptin, metformin hydroklorid - 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 och 5. 1 för tillgänglig data på olika kombinationer).