Tesavel Den europeiske union - norsk - EMA (European Medicines Agency)

tesavel

merck sharp & dohme b.v. - sitagliptin - diabetes mellitus, type 2 - legemidler som brukes i diabetes - for pasienter med type-2 diabetes mellitus, tesavel er indikert for å bedre glykemisk kontroll:som monoterapi:hos pasienter som ikke kontrolleres av kosthold og mosjon alene og for hvem metformin er uhensiktsmessig pga. kontraindikasjoner eller intoleranse;som dual oral terapi i kombinasjon med metformin, når diett og trening pluss metformin alene ikke gir tilstrekkelig glykemisk kontroll;en sulphonylurea når diett og trening pluss maksimal tolerert dose av en sulphonylurea alene ikke gir tilstrekkelig glykemisk kontroll, og når metformin er uhensiktsmessig pga. kontraindikasjoner eller intoleranse;en ppary agonist (jeg. en thiazolidinedione) ved bruk av en ppary agonist er hensiktsmessig og når diett og trening pluss ppary agonist alene ikke gir tilstrekkelig glykemisk kontroll;som trippel oral terapi i kombinasjon witha sulphonylurea og metformin når diett og mosjon plus dobbel behandling med disse midler ikke gir tilstrekkelig glykemisk kontroll;en peroxisome-proliferator-aktivert reseptor-gamma (ppary) agonist og metformin når bruken av en ppary agonist er hensiktsmessig og når diett og mosjon plus dobbel behandling med disse midler ikke gir tilstrekkelig glykemisk kontroll. tesavel er også angitt som legg til på insulin (med eller uten metformin) når diett og trening pluss stabil dosering av insulin ikke gir tilstrekkelig glykemisk kontroll.

Nytox vet 1000 mg/ g Norge - norsk - Statens legemiddelverk

nytox vet 1000 mg/ g

naqua ltd - trikainmesilat - pulver til behandlingsoppløsning til fisk - 1000 mg/ g

Tricaine Pharmaq 1000 mg/ g Norge - norsk - Statens legemiddelverk

tricaine pharmaq 1000 mg/ g

pharmaq as, overhalla - trikainmesilat - pulver til behandlingsoppløsning til fisk - 1000 mg/ g

Venorion 75 mg Norge - norsk - Statens legemiddelverk

venorion 75 mg

orion corporation - espoo - venlafaksinhydroklorid - depotkapsel, hard - 75 mg

Venorion 37.5 mg Norge - norsk - Statens legemiddelverk

venorion 37.5 mg

orion corporation - espoo - venlafaksinhydroklorid - depotkapsel, hard - 37.5 mg

Venorion 150 mg Norge - norsk - Statens legemiddelverk

venorion 150 mg

orion corporation - espoo - venlafaksinhydroklorid - depotkapsel, hard - 150 mg

Roclanda Den europeiske union - norsk - EMA (European Medicines Agency)

roclanda

santen oy - latanoprost, netarsudil mesilate - glaucoma, open-angle; ocular hypertension - Øyemidler - roclanda is indicated for the reduction of elevated intraocular pressure (iop) in adult patients with primary open-angle glaucoma or ocular hypertension for whom monotherapy with a prostaglandin or netarsudil provides insufficient iop reduction.

Sitagliptin SUN Den europeiske union - norsk - EMA (European Medicines Agency)

sitagliptin sun

sun pharmaceutical industries europe b.v. - sitagliptin fumarate - diabetes mellitus, type 2 - legemidler som brukes i diabetes - 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.

Sitagliptin Accord Den europeiske union - norsk - EMA (European Medicines Agency)

sitagliptin accord

accord healthcare s.l.u. - sitagliptin hydrochloride - diabetes mellitus, type 2 - legemidler som brukes i diabetes - for adult patients with type 2 diabetes mellitus, sitagliptin accord 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 (ppary) agonist (i. a thiazolidinedione) when use of a ppary agonist is appropriate and when diet and exercise plus the ppary 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 ppary agonist and metformin when use of a ppary agonist is appropriate and when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control. sitagliptin accord 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.

Sitagliptin / Metformin hydrochloride Accord Den europeiske union - norsk - EMA (European Medicines Agency)

sitagliptin / metformin hydrochloride accord

accord healthcare s.l.u. - metformin hydrochloride, sitagliptin hydrochloride monohydrate - diabetes mellitus, type 2 - legemidler som brukes i diabetes - 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. triple kombinasjon terapi) som et tillegg til diett og trening hos pasienter ikke kontrollert på deres maksimal tolerert dose av metformin og en sulphonylurea. 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.