União Europeia - estoniano - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - live recombinant marek’s disease (md) virus, serotype 1, strain rn1250 - immunoloogilised ained - kana - for active immunisation of one-day-old chicks to prevent mortality and clinical signs and reduce lesions caused by marek’s disease (md) virus (including very virulent md virus).

União Europeia - estoniano - EMA (European Medicines Agency)

ceva-phylaxia veterinary biologicals co. ltd - turkey herpes virus, strain rhvt/nd/ibd, expressing the fusion protein of newcastle disease virus and the vp2 protein of infectious bursal disease virus, live recombinant - immunoloogilised ained - embryonated chicken eggs; chicken - for the active immunisation of one-day-old chicks or 18-day-old chicken embryonated eggs to reduce mortality, clinical signs and lesions caused by newcastle disease virus (ndv) and to reduce virus shedding; to reduce mortality, clinical signs and bursa lesions caused by very virulent infectious bursal disease virus (ibdv); to reduce mortality, clinical signs and lesions caused by classical marek’s disease virus (mdv).

União Europeia - estoniano - EMA (European Medicines Agency)

tigenix n.v. - mida iseloomustab elujõuline autoloogse kõhrerakke laiendatud ex vivo väljendada konkreetsete marker valkude - kõhrehaigused - muud lihas-skeleti süsteemi häirete ravimid - põlveliigese reieluupõletiku (rahvusvaheline kõhreparanduse ühiskond (icrs) iii või iv klassi üksikute sümptomaatiliste kõhrefunktsioonide parandamine täiskasvanutel). samaaegne asümptomaatiline kõhre kahjustused (varude muutuse aruannet klassi i või ii) võib esineda. tõendamine efektiivsus põhineb randomiseeritud kontrollitud uuringus hindamise efektiivsust chondrocelect patsientidel kahjustused vahel 1 ja 5 cm2.

União Europeia - estoniano - EMA (European Medicines Agency)

mediwound germany gmbh - proteolytic enzymes enriched in bromelain - debridement - preparaadid haavade ja haavandite raviks - nexobrid on näidustatud eschari eemaldamiseks täiskasvanutel, kellel on sügavad osalise ja täispikkusega termilised põletused.

União Europeia - estoniano - 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.

União Europeia - estoniano - EMA (European Medicines Agency)

gilead sciences ireland uc, galapagos nv - filgotinib maleate - artriit, reumatoidartriit - immunosupressandid - rheumatoid arthritisjyseleca 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). jyseleca may be used as monotherapy or in combination with methotrexate (mtx). ulcerative colitisjyseleca is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a biologic agent.

União Europeia - estoniano - EMA (European Medicines Agency)

intervet international bv - orbifloxacin, mometasone furoaat, posaconazole - otoloogilised omadused - koerad - ravi ägeda otitis externa ja ägeda ägenemised korduv otitis externa, mis on seotud bakterite vastuvõtlikud orbifloxacin ja seened vastuvõtlikud posaconazole, eriti malassezia pachydermatis.

União Europeia - estoniano - EMA (European Medicines Agency)

merck sharp dohme ltd - inimese papilloomiviiruse tüübi 6 l1-proteiini, inimese papilloomiviiruse tüübi 11 l1-proteiini, inimese papilloomiviiruse tüübi 16 l1-proteiini, inimese papilloomiviiruse tüübi 18 l1-proteiini - papillomavirus infections; uterine cervical dysplasia; condylomata acuminata; immunization - vaktsiinid - silgard on vaktsiin kasutamiseks vanuses 9 aastat ennetamise:premalignant suguelundite kahjustused (emakakaela, vulvar ja tupe), premalignant anal kahjustused, emakakaela vähk ja päraku vähk põhjuslikult seotud teatavate oncogenic inimese papilloomiviiruse (hpv) tüübid;suguelundite tüükad (condyloma acuminata) põhjuslikult seotud kindlate hpv tüübid. vt lõigud 4. 4 ja 5. 1, et saada olulist teavet selle näidustust toetavate andmete kohta. kasutada silgard peab olema kooskõlas ametlike soovitustega.

União Europeia - estoniano - EMA (European Medicines Agency)

smithkline beecham plc - rosiglitasoon - suhkurtõbi, tüüp 2 - diabeetis kasutatavad ravimid - rosiglitazone on näidustatud ravi 2. tüüpi suhkurtõve:kui monotherapy-patsientidel (eelkõige ülekaalulistel patsientidel) ebapiisavalt kontrollitud toitumise ja treeningu kohta, kellele metformiin ei sobi, sest vastunäidustused või intoleranceas dual suukaudne ravi kombinatsioonis-metformiin, patsientidel (eriti ülekaalulistel patsientidel), millel piisavalt glycaemic kontrolli hoolimata maksimaalne talutav annus monotherapy koos metformiin-sulphonylurea, ainult patsientidel, kes näitavad, sallimatuse, et metformiin või kellele metformiin on vastunäidustatud, ebapiisav glycaemic kontrolli hoolimata monotherapy koos sulphonylureaas kolmekordse suukaudse ravi kombinatsioonis-metformiin ja sulphonylurea, patsientidel (eriti ülekaalulistel patsientidel), millel piisavalt glycaemic kontrolli hoolimata dual suukaudne ravi (vt lõik 4.

União Europeia - estoniano - EMA (European Medicines Agency)

laboratoires delbert - histamiini dihüdrokloriid - leukeemia, müeloidne, äge - immunostimulants, - ceplene maintenance therapy is indicated for adult patients with acute myeloid leukaemia in first remission concomitantly treated with interleukin-2 (il-2). ceplene efektiivsus ei ole täielikult tõestatud üle 60-aastastel patsientidel.