Sitagliptin / Metformin hydrochloride Mylan Euroopa Liit - eesti - EMA (European Medicines Agency)

sitagliptin / metformin hydrochloride mylan

mylan ireland limited - sitagliptin hydrochloride monohydrate, metformin hydrochloride - suhkurtõbi, tüüp 2 - diabeetis kasutatavad ravimid - 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. , kolmekordne kombineeritud ravi) lisandina toitumise ja treeningu patsientidel, ebapiisavalt kontrollitud nende maksimaalne talutav annus metformiin ja 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.

Sitagliptin Accord Euroopa Liit - eesti - EMA (European Medicines Agency)

sitagliptin accord

accord healthcare s.l.u. - sitagliptin hydrochloride - suhkurtõbi, tüüp 2 - diabeetis kasutatavad ravimid - 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 Euroopa Liit - eesti - EMA (European Medicines Agency)

sitagliptin / metformin hydrochloride accord

accord healthcare s.l.u. - metformin hydrochloride, sitagliptin hydrochloride monohydrate - suhkurtõbi, tüüp 2 - diabeetis kasutatavad ravimid - 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. , kolmekordne kombineeritud ravi) lisandina toitumise ja treeningu patsientidel, ebapiisavalt kontrollitud nende maksimaalne talutav annus metformiin ja 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.

Carbaglu Euroopa Liit - eesti - EMA (European Medicines Agency)

carbaglu

recordati rare diseases - karglumhape - amino acid metabolism, inborn errors; propionic acidemia - muud alimentary seedetrakti ja ainevahetust tooted, - carbaglu on näidustatud ravi:hyperammonaemia tõttu n-acetylglutamate-synthase esmane puudus;hyperammonaemia tõttu isovaleric acidaemia;hyperammonaemia tõttu methymalonic acidaemia;hyperammonaemia tõttu propioonhappe acidaemia.

Nobilis Rismavac süstesuspensiooni kontsentraat ja lahusti Eesti - eesti - Ravimiamet

nobilis rismavac süstesuspensiooni kontsentraat ja lahusti

intervet international b.v. - lindude herpesviirusvaktsiin (mareki haigus) - süstesuspensiooni kontsentraat ja lahusti - 5000annus 1tk; 1000annus 1tk; 4000annus 1tk; 2000annus 1tk

Nobilis Rismavac + CA126 süstesuspensiooni kontsentraat ja lahusti Eesti - eesti - Ravimiamet

nobilis rismavac + ca126 süstesuspensiooni kontsentraat ja lahusti

intervet international b.v. - lindude herpesviirusvaktsiin (mareki haigus) - süstesuspensiooni kontsentraat ja lahusti - 4000annus 1tk; 1000annus 1tk; 5000annus 1tk

Nobilis Marexine CA 126 süstesuspensiooni kontsentraat ja lahusti Eesti - eesti - Ravimiamet

nobilis marexine ca 126 süstesuspensiooni kontsentraat ja lahusti

intervet international b.v. - lindude herpesviirusvaktsiin (mareki haigus) - süstesuspensiooni kontsentraat ja lahusti - 1000pfu 1annus 2000annus 1tk; 1000pfu 1annus 1000annus 1tk

Ucedane Euroopa Liit - eesti - EMA (European Medicines Agency)

ucedane

eurocept international bv - karglumhape - hyperammonemia; amino acid metabolism, inborn errors - muud alimentary seedetrakti ja ainevahetust tooted, - ucedane is indicated in treatment of:hyperammonaemia due to n-acetylglutamate synthase primary deficiency;hyperammonaemia due to isovaleric acidaemia;hyperammonaemia due to methymalonic acidaemia;hyperammonaemia due to propionic acidaemia.

Cevac MD HVT süstesuspensiooni kontsentraat ja lahusti Eesti - eesti - Ravimiamet

cevac md hvt süstesuspensiooni kontsentraat ja lahusti

ceva-phylaxia zrt. - lindude herpesviirusvaktsiin (mareki haigus) - süstesuspensiooni kontsentraat ja lahusti - 1000annus 1tk; 4000annus 1tk; 2000annus 1tk

Novamune süstesuspensiooni kontsentraat ja lahusti Eesti - eesti - Ravimiamet

novamune süstesuspensiooni kontsentraat ja lahusti

ceva-phylaxia zrt. - lindude nakkava bursiidi (gumboro) viirusvaktsiin - süstesuspensiooni kontsentraat ja lahusti - 1000annus 1tk; 500annus 1tk