Estonja - Estonjan - Ravimiamet

sandoz pharmaceuticals d.d. - trimetasidiin - toimeainet modifitseeritult vabastav tablett - 35mg 30tk; 35mg 10tk; 35mg 60tk; 35mg 40tk; 35mg 90tk

Unjoni Ewropea - Estonjan - EMA (European Medicines Agency)

kyowa kirin holdings b.v. - naloksegooli oksalaat - constipation; opioid-related disorders - perifeerne opioidi retseptori antagonistid, uimastid, kõhukinnisus - opioidi poolt indutseeritud kõhukinnisuse ravi (oic) täiskasvanud patsientidel, kellel on ebapiisav vastus lahtistidele (-lubadele).

Unjoni Ewropea - Estonjan - EMA (European Medicines Agency)

merck sharp & dohme b.v. - bezlotoxumab - pseudomembranoosne enterokoliit - suguhormoonid ja immunoglobuliinid, - zinplava on näidustatud clostridium difficile infektsiooni (cdi) kordumise ennetamiseks täiskasvanutel, kellel on kõrge risk cdi-d.

Unjoni Ewropea - Estonjan - EMA (European Medicines Agency)

merck sharp dohme ltd  - peginterferoon alfa-2b - c-hepatiit, krooniline - immunostimulants, - adults (tritherapy)viraferonpeg in combination with ribavirin and boceprevir (tritherapy) is indicated for the treatment of chronic-hepatitis-c (chc) genotype-1 infection in adult patients (18 years of age and older) with compensated liver disease who are previously untreated or who have failed previous therapy. palun vaadake ribavirin ja boceprevir ravimi omaduste kokkuvõtted (smpcs) kui viraferonpeg on kasutada koos nende ravimitega. adults (bitherapy and monotherapy)viraferonpeg is indicated for the treatment of adult patients (18 years of age and older) with chc who are positive for hepatitis-c-virus rna (hcv-rna), including patients with compensated cirrhosis and / or co-infected with clinically stable hiv. viraferonpeg koos ribavirin (bitherapy) on näidustatud ravi chc nakkuse täiskasvanud patsientidel, kes on eelnevalt ravimata, sealhulgas patsientidel, kellel on kliiniliselt stabiilne hiv-nakkus ja täiskasvanud patsientidel, kes on jätnud eelnev ravi interferoon alfa (pegylated või mitte-pegylated) ja ribavirin kombinatsiooni teraapia või interferoon alfa monotherapy. interferoon monotherapy, sh viraferonpeg on näidustatud peamiselt juhul, talumatus või vastunäidustus, et ribavirin. palun vaadake ribavirin ravimi omaduste kokkuvõte, kui viraferonpeg on kasutada koos ribavirin. paediatric population (bitherapy)viraferonpeg is indicated in a combination regimen with ribavirin for the treatment of children three years of age and older and adolescents, who have chronic hepatitis c, previously untreated, without liver decompensation, and who are positive for hcv-rna. kui otsustatakse, et ei ravi edasi lükata, kuni täiskasvanueani, on tähtis arvestada, et kombineeritud ravi tingitud majanduskasvu pidurdumine, mis võib olla pöördumatu mõnedel patsientidel. otsus ravida, tuleb teha iga juhtumi puhul eraldi. palun vaadake ribavirin ravimi omaduste kokkuvõte kapslite või suukaudse lahuse kui viraferonpeg on kasutada koos ribavirin.

Unjoni Ewropea - Estonjan - EMA (European Medicines Agency)

serb sas - telotristat etipraat - carcinoid tumor; neuroendocrine tumors - muud seedetrakti ja ainevahetustooted - xermelo on näidustatud carcinoid sündroom kõhulahtisus koos somatostatiini analoog (ssa) ravi piisavalt kontrollitud, ssa ravi täiskasvanutel.

Unjoni Ewropea - Estonjan - EMA (European Medicines Agency)

astrazeneca ab - saxagliptin - suhkurtõbi, tüüp 2 - diabeetis kasutatavad ravimid - add-on combination therapyonglyza is indicated in adult patients aged 18 years and older with type-2 diabetes mellitus 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 metformin alone, with diet and exercise, does not provide adequate glycaemic control;in combination with a sulphonylurea, when the sulphonylurea alone, with diet and exercise, does not provide adequate glycaemic control in patients for whom use of metformin is considered inappropriate;in combination with a thiazolidinedione, when the thiazolidinedione alone with diet and exercise, does not provide adequate glycaemic control in patients for whom use of a thiazolidinedione is considered appropriate;as triple oral therapy:in combination with metformin plus a sulphonylurea when this regimen alone, with diet and exercise, does not provide adequate glycaemic control;as combination therapy with insulin (with or without metformin), when this regimen alone, with diet and exercise, does not provide adequate glycaemic control.