zyrtec suukaudne lahus
ucb pharma oy finland - tsetirisiin - suukaudne lahus - 1mg 1ml 150ml 1tk; 1mg 1ml 75ml 1tk; 1mg 1ml 100ml 1tk; 1mg 1ml 200ml 1tk
levodonna tablett
sandoz pharmaceuticals d.d. - levonorgestreel - tablett - 1500mcg 1tk
zyrtec suukaudsed tilgad, lahus
globalex pharma oÜ - tsetirisiin - suukaudsed tilgad, lahus - 10mg 1ml 20ml 1tk
idefirix
hansa biopharma ab - imlifidase - desensitization, immunologic; kidney transplantation - immunosupressandid - idefirix is indicated for desensitisation treatment of highly sensitised adult kidney transplant patients with positive crossmatch against an available deceased donor. the use of idefirix should be reserved for patients unlikely to be transplanted under the available kidney allocation system including prioritisation programmes for highly sensitised patients.
zyrtec suukaudsed tilgad, lahus
lex ano uab - tsetirisiin - suukaudsed tilgad, lahus - 10mg 1ml 20ml 1tk
zyrtec õhukese polümeerikattega tablett
lex ano uab - tsetirisiin - õhukese polümeerikattega tablett - 10mg 30tk
postinor suus dispergeeruv tablett
gedeon richter plc. - levonorgestreel - suus dispergeeruv tablett - 1,5mg 1tk
aranesp
amgen europe b.v. - darbepoetiin alfa - anemia; cancer; kidney failure, chronic - muud antianemic preparaadid - kroonilise neerupuudulikkusega (crf) seotud sümptomaatilise aneemia ravi täiskasvanutel ja lastel. ravi on sümptomaatiline aneemia täiskasvanud vähiga patsientidel, kellel on mitte-müeloidne malignancies saanud keemiaravi.
avonex
biogen netherlands b.v. - interferoon beeta-1a - hulgiskleroos - immunostimulants, - avonex on näidustatud ravi:patsiente, kellel on diagnoositud relapsing sclerosis multiplex (ms). kliinilistes uuringutes, oli see, mida iseloomustavad kahe või enama akuutse ägenemised (ägenemiste) viimase kolme aasta jooksul ilma tõendeid pidev progressioon vahel ägenemiste; avonex aeglustab kasvamist puude ja vähendab ägenemiste sagedus;patsiendid, kellel on ühe demüeliniseerivate juhul koos aktiivse põletikulise protsessi, kui see on piisavalt tõsine, et õigustada ravi intravenoosselt kortikosteroide, kui alternatiivsed diagnoosid on välistatud, ja kui nad on kindlaks tehtud, et on suur risk haigestuda kliiniliselt kindel ms. avonex tuleb katkestada patsientidel, kellel tekivad progressiivne ms.
blincyto
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.