Euroopa Liit - eesti - EMA (European Medicines Agency)

sanofi-aventis deutschland gmbh - insulin human - diabeet mellitus - diabeetis kasutatavad ravimid - suhkurtõbi, kus on vaja insuliiniravi. insuliini inimese winthrop kiire sobib ka millega kaasnes hüperglükeemiline kooma ja ketoatsidoos, samuti saavutada enne, intra - ja postoperatiivne stabiilsuse patsientidel, kellel.

Euroopa Liit - eesti - EMA (European Medicines Agency)

sanofi winthrop industrie - insuliin lispro - diabeet mellitus - diabeetis kasutatavad ravimid - suhkurtõvega täiskasvanute ja laste raviks, kes vajavad insuliini normaalse glükoosi homöostaasi säilitamiseks. insuliin lispro sanofi on näidustatud ka suhkurtõve esialgseks stabiliseerimiseks.

Euroopa Liit - eesti - EMA (European Medicines Agency)

sanofi winthrop industrie - aspartinsuliin - diabeet mellitus - diabeetis kasutatavad ravimid - insulin aspart sanofi is indicated for the treatment of diabetes mellitus in adults, adolescents and children aged 1 year and above.

Euroopa Liit - eesti - EMA (European Medicines Agency)

accord healthcare s.l.u. - metformin hydrochloride, vildagliptin - suhkurtõbi, tüüp 2 - diabeetis kasutatavad ravimid - vildagliptin/metformin hydrochloride accord 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 ja 5. 1 erinevate kombinatsioonide kohta kättesaadavate andmete osas).

Euroopa Liit - eesti - EMA (European Medicines Agency)

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.

Euroopa Liit - eesti - EMA (European Medicines Agency)

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.

Euroopa Liit - eesti - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - sitagliptin fumarate, metformin hydrochloride - suhkurtõbi, tüüp 2 - diabeetis kasutatavad ravimid - for adult patients with type 2 diabetes mellitus:sitagliptin/metformin hydrochloride sun 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 sun 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 sun 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. sitagliptin/metformin hydrochloride sun 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.

Euroopa Liit - eesti - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - insulin human - insulins ja analoogi jaoks süsti, keskmise toimeajaga - cats; dogs - ravi diabeedi kassid ja koerad, et saavutada vähendamine hüperglükee ja parandamisega seotud kliinilised nähud.

Euroopa Liit - eesti - EMA (European Medicines Agency)

sanofi-aventis deutschland gmbh - insulin human - diabeet mellitus - diabeetis kasutatavad ravimid - suhkurtõbi, kus on vaja insuliiniravi. insuman rapid on ka sobiv, millega kaasnes hüperglükeemiline kooma ja ketoatsidoos, samuti saavutada enne, intra - ja postoperatiivne stabiilsuse patsientidel, kellel.

Euroopa Liit - eesti - EMA (European Medicines Agency)

pfizer limited - insulin human - diabeet mellitus - diabeetis kasutatavad ravimid - exubera on näidustatud ravi täiskasvanud patsientidel, kellel on tüüp 2 diabeet notadequately kontrollitud suukaudsete antidiabetic ained ja vajavad insuliini ravi. exubera on näidustatud ka ravi täiskasvanud patsientidel, kellel on 1. tüüpi diabeet, inaddition, et pikad või keskmise toimeajaga insuliini subkutaanse, kelle potentsiaalne kasu ofadding inhaleeritava insuliini kaalub üles võimaliku ohutuse probleeme (vt lõik 4.