Eesti - eesti - Ecolab

ecolab deutschland gmbh -

Euroopa Liit - eesti - EMA (European Medicines Agency)

ceva-phylaxia co. ltd. - live recombinant fowlpox virus expressing the membrane fusion protein and the encapsidation protein of avian infectious laryngotracheitis virus (rfp-lt) and avian encephalomyelitis virus, strain calnek 1143 (ae) - immunologicals for aves, live viral vaccines, domestic fowl - kana - for active immunisation of chickens of 8 to 13 weeks of age in order to reduce the skin lesions due to fowlpox, to reduce the clinical signs and tracheal lesions due to avian infectious laryngotracheitis and to prevent egg production losses due to avian encephalomyelitis.

Euroopa Liit - eesti - EMA (European Medicines Agency)

almirall, s.a. - tirbanibulin - keratoos, actinic - antibiootikumid ja kemoterapeutikumid dermatoloogiliseks kasutamiseks - klisyri is indicated for the field treatment of non-hyperkeratotic, non-hypertrophic actinic keratosis (olsen grade 1) of the face or scalp in adults.

Euroopa Liit - eesti - EMA (European Medicines Agency)

ceva-phylaxia co. ltd. - recombinant fowlpox virus expressing the membrane fusion protein and the encapsidation protein of avian infectious laryngotracheitis virus, live - kana - for active immunisation of chickens from 8 weeks of age in order to reduce the skin lesions due to fowlpox and to reduce the clinical signs and tracheal lesions due to avian infectious laryngotracheitis.

Euroopa Liit - eesti - 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.

Euroopa Liit - eesti - EMA (European Medicines Agency)

helsinn birex pharmaceuticals ltd. - palonosetroonvesinikkloriid - vomiting; cancer - antiemeetikumid ja antinauseants, , serotoniini (5ht3) antagonistid - aloxi on näidustatud täiskasvanutel:ennetamiseks äge iiveldus ja oksendamine, mis on seotud väga emetogenic vähk, kemoteraapia,ennetamine iiveldus ja oksendamine on seotud mõõdukalt emetogenic vähi keemiaravi. aloxi on näidustatud pediaatrilised patsiendid 1 kuu vanused ja vanemad:ennetamiseks äge iiveldus ja oksendamine, mis on seotud väga emetogenic vähi keemiaravi ja ennetamine iiveldus ja oksendamine on seotud mõõdukalt emetogenic vähi keemiaravi.

Euroopa Liit - eesti - EMA (European Medicines Agency)

the medicines company uk ltd - bivalirudin - Äge koronaarsündroom - antitrombootilised ained - angiox on näidustatud on antikoagulant täiskasvanud patsientidel toimumas perkutaanse koronaarse interventsiooni (pci), sealhulgas patsiendid, kellel on st-segmendi-elevatsiooniga müokardiinfarkti (stemi) toimumas primaarne pci. angiox on näidustatud ka ravi täiskasvanud patsientidel, kellel ebastabiilne stenokardia / mitte-st-segmendi-elevatsiooniga müokardiinfarkti (ua / nstemi) planeeritud kiiresti või varajane sekkumine. angiox tuleb manustada koos aspiriini ja clopidogrel.

Euroopa Liit - eesti - 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.

Euroopa Liit - eesti - EMA (European Medicines Agency)

pfizer europe ma eeig - nonacog alfa - hemofiilia b - antihemorraagilised ained - veritsuste ravi ja profülaktika hemofiilia b (kaasasündinud faktori ix puudulikkus) patsientidel.

Euroopa Liit - eesti - EMA (European Medicines Agency)

amgen europe b.v. - blinatumomab - prekursorko-lümfoblastne leukeemia-lümfoom - antineoplastilised ained - blincyto is indicated as monotherapy for the treatment of adults with cd19 positive relapsed or refractory b precursor acute lymphoblastic leukaemia (all). patients with philadelphia chromosome positive b-precursor all should have failed treatment with at least 2 tyrosine kinase inhibitors (tkis) and have no alternative treatment options. blincyto is indicated as monotherapy for the treatment of adults with philadelphia chromosome negative cd19 positive b-precursor all in first or second complete remission with minimal residual disease (mrd) greater than or equal to 0. blincyto is indicated as monotherapy for the treatment of paediatric patients aged 1 year or older with philadelphia chromosome negative cd19 positive b precursor all which is refractory or in relapse after receiving at least two prior therapies or in relapse after receiving prior allogeneic haematopoietic stem cell transplantation. blincyto is indicated as monotherapy for the treatment of paediatric patients aged 1 year or older with high-risk first relapsed philadelphia chromosome negative cd19 positive b-precursor all as part of the consolidation therapy (see section 4.