MULTIBIC POTASSIUM-FREE hemodialüüsi-/hemofiltratsioonilahus Естония - естонски - Ravimiamet

multibic potassium-free hemodialüüsi-/hemofiltratsioonilahus

fresenius medical care deutschland gmbh - naatriumkloriid+kaltsiumkloriiddihüdraat+magneesiumkloriid+glükoos+naatriumvesinikkarbonaat - hemodialüüsi-/hemofiltratsioonilahus - 6,048g+0,2205g+0,1016g+1,1g+3,066g 1l 5000ml 2tk

DUOSOL ILMA KAALIUMITA hemofiltratsioonilahus Естония - естонски - Ravimiamet

duosol ilma kaaliumita hemofiltratsioonilahus

b. braun avitum ag - naatriumkloriid+kaltsiumkloriiddihüdraat+magneesiumkloriid+glükoos+naatriumvesinikkarbonaat - hemofiltratsioonilahus - 4,21g+1,98g+0,91g+9,9g+0/6,18g+0+0+0+3,59g 1000ml 555ml 2tk / 4445ml 2tk

KALII CHLORIDUM/GLUCOSUM B. BRAUN 1,5 MG/ML + 50 MG/ML infusioonilahus Естония - естонски - Ravimiamet

kalii chloridum/glucosum b. braun 1,5 mg/ml + 50 mg/ml infusioonilahus

b. braun melsungen ag - kaaliumkloriid+glükoos - infusioonilahus - 1,5g+50g 1l 500ml 10tk

Calciject PMD süstelahus Естония - естонски - Ravimiamet

calciject pmd süstelahus

norbrook laboratories limited - kaltsiumglükonaat+boorhape+glükoos+magneesiumhüpofosfit - süstelahus - 166mg+34mg+220mg+50mg 1ml 400ml 1tk

Mounjaro Европейски съюз - естонски - EMA (European Medicines Agency)

mounjaro

eli lilly nederland b.v. - tirzepatide - suhkurtõbi, tüüp 2 - diabeetis kasutatavad ravimid - mounjaro is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise- as monotherapy when metformin is considered inappropriate due to intolerance or contraindications- in addition to other medicinal products for the treatment of diabetes. for study results with respect to combinations, effects on glycaemic control and the populations studied, see sections 4. 4, 4. 5 ja 5.

Apidra Европейски съюз - естонски - EMA (European Medicines Agency)

apidra

sanofi-aventis deutschland gmbh - insuliinglulisiin - diabeet mellitus - diabeetis kasutatavad ravimid - ravi täiskasvanud, noorukid ja lapsed, kuue-aastased või vanemad, suhkurtõbi, kui ravi insuliin on nõutav.

Eucreas Европейски съюз - естонски - EMA (European Medicines Agency)

eucreas

novartis europharm limited - vildagliptin, metformiin vesinikkloriid - suhkurtõbi, tüüp 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.

Fiasp Европейски съюз - естонски - EMA (European Medicines Agency)

fiasp

novo nordisk a/s - aspartinsuliin - diabeet mellitus - drugs used in diabetes, insulins and analogues for injection, fast-acting - suhkurtõve ravi täiskasvanutel, noorukitel ja 1-aastastel ja vanematel lastel.

Icandra (previously Vildagliptin / metformin hydrochloride Novartis) Европейски съюз - естонски - EMA (European Medicines Agency)

icandra (previously vildagliptin / metformin hydrochloride novartis)

novartis europharm limited - vildagliptin, metformiin vesinikkloriid - suhkurtõbi, tüüp 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 ja 5. 1 erinevate kombinatsioonide kohta kättesaadavate andmete osas).

Incresync Европейски съюз - естонски - EMA (European Medicines Agency)

incresync

takeda pharma a/s - alogliptin, pioglitazone - suhkurtõbi, tüüp 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - incresync is indicated as a second- or third-line treatment in adult patients aged 18 years and older with type-2 diabetes mellitus: , as an adjunct to diet and exercise to improve glycaemic control in adult patients (particularly overweight patients) inadequately controlled on pioglitazone alone, and for whom metformin is inappropriate due to contraindications or intolerance;, in combination with metformin (i. kolmekordne kombineeritud ravi) lisandina toitumise ja treeningu parandamiseks glycaemic kontrolli täiskasvanud patsientidel (eelkõige ülekaalulistel patsientidel) ebapiisavalt kontrollitud nende maksimaalne talutav annus metformiin ja pioglitazone. lisaks incresync saab kasutada, et asendada eraldi tabletid alogliptin ja pioglitazone neil täiskasvanud patsientidel vanuses 18 aastat ja vanemad, koos tüüp-2 diabeet juba ravitakse see kombinatsioon. pärast algatamist ravi incresync, patsiente tuleks läbi vaadata pärast kolme kuni kuue kuu jooksul, et hinnata piisavust ravi (e. vähendada hba1c). patsientidel, kes ei näita piisava vastuse, incresync tuleks lõpetada. arvestades võimalikke riske pikaajalise pioglitazone ravi, arstid tuleks kinnitada järgmiste korraliste kommentaare, mis kasu incresync on säilinud (vt lõik 4.