Estónsko - estónčina - Ravimiamet

teva b.v. - oktreotiid - toimeainet prolongeeritult vabastava süstesuspensiooni pulber ja lahusti - 30mg 1tk

Estónsko - estónčina - Ravimiamet

sandoz pharmaceuticals d.d. - takroliimus - toimeainet prolongeeritult vabastav kõvakapsel - 1mg 50tk; 1mg 100tk; 1mg 30tk; 1mg 60tk

Estónsko - estónčina - Ravimiamet

sandoz pharmaceuticals d.d. - takroliimus - toimeainet prolongeeritult vabastav kõvakapsel - 5mg 100tk; 5mg 50tk; 5mg 30tk; 5mg 60tk

Estónsko - estónčina - Ravimiamet

sandoz pharmaceuticals d.d. - takroliimus - toimeainet prolongeeritult vabastav kõvakapsel - 3mg 30tk; 3mg 50tk; 3mg 60tk

Estónsko - estónčina - Ravimiamet

sandoz pharmaceuticals d.d. - takroliimus - toimeainet prolongeeritult vabastav kõvakapsel - 0,5mg 50tk; 0,5mg 30tk; 0,5mg 60tk

Estónsko - estónčina - Ravimiamet

sandoz pharmaceuticals d.d. - takroliimus - toimeainet prolongeeritult vabastav kõvakapsel - 2mg 100tk; 2mg 60tk; 2mg 50tk

Európska únia - estónčina - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - upadacitinib - artriit, reumatoidartriit - immunosupressandid - rheumatoid arthritisrinvoq is indicated for the treatment of moderate to severe active rheumatoid arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more disease-modifying anti-rheumatic drugs (dmards). rinvoq may be used as monotherapy or in combination with methotrexate. psoriatic arthritisrinvoq is indicated for the treatment of active psoriatic arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more dmards. rinvoq may be used as monotherapy or in combination with methotrexate. axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)rinvoq is indicated for the treatment of active non-radiographic axial spondyloarthritis in adult patients with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri), who have responded inadequately to nonsteroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)rinvoq is indicated for the treatment of active ankylosing spondylitis in adult patients who have responded inadequately to conventional therapy. atopic dermatitisrinvoq is indicated for the treatment of moderate to severe atopic dermatitis in adults and adolescents 12 years and older who are candidates for systemic therapy. ulcerative colitisrinvoq is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.  crohn’s diseaserinvoq is indicated for the treatment of adult patients with moderately to severely active crohn’s disease who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.

Európska únia - estónčina - EMA (European Medicines Agency)

ucb pharma s.a.   - bimekizumab - psoriaas - immunosupressandid - plaque psoriasisbimzelx is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisbimzelx, alone or in combination with methotrexate, is indicated for the treatment of active psoriatic arthritis in adults who have had an inadequate response or who have been intolerant to one or more disease-modifying antirheumatic drugs (dmards). axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)bimzelx is indicated for the treatment of adults with active non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri) who have responded inadequately or are intolerant to non-steroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)bimzelx is indicated for the treatment of adults with active ankylosing spondylitis who have responded inadequately or are intolerant to conventional therapy.

Estónsko - estónčina - Ravimiamet

adamed pharma s.a. - tamsulosiin+solifenatsiin - toimeainet modifitseeritult vabastav tablett - 0,4mg+6mg 30tk; 0,4mg+6mg 60tk

Európska únia - estónčina - EMA (European Medicines Agency)

cheplapharm arzneimittel gmbh - pioglitasoonvesinikkloriid - suhkurtõbi, tüüp 2 - diabeetis kasutatavad ravimid - pioglitazone on näidustatud ravi tüüp-2 diabeet:kui monotherapy:patsientidel (eelkõige ülekaalulistel patsientidel) ebapiisavalt kontrollitud toitumise ja treeningu kohta, kellele metformiin ei sobi, sest vastunäidustusi või talumatust;as dual suukaudne ravi koos:metformiin, patsientidel (eriti ülekaalulistel patsientidel), millel piisavalt glycaemic kontrolli hoolimata maksimaalne talutav annus monotherapy koos metformiin;a sulphonylurea, ainult patsientidel, kes näitavad, sallimatuse, et metformiin või kellele metformiin on vastunäidustatud, ebapiisav glycaemic kontrolli hoolimata maksimaalne talutav annus monotherapy koos sulphonylurea;kui kolmekordse suukaudse ravi koos:metformiin ja sulphonylurea, patsientidel (eriti ülekaalulistel patsientidel), millel piisavalt glycaemic kontrolli hoolimata dual suukaudne ravi. pioglitazone on ka näidatud koos insuliini tüüp-2 diabeet patsiendid, kellel on ebapiisav glycaemic kontrolli insuliini, kellele metformiin ei sobi, sest vastunäidustusi või talumatust.