stelfonta
qbiotics netherlands b.v. - tigilanol tiglate - tigilanol tiglate - Šunys - gydyti ne resectable, ne metastazavusio (kurie sustojimo) poodinio putliųjų ląstelių navikai įsikūręs, ar distalinės į alkūnės arba kulno, ir ne resectable, neišplitusia odos putliųjų ląstelių navikų šunys.
human igg1 monoclonal antibody specific for human interleukin-1 alpha xbiotech
xbiotech germany gmbh - žmogaus igg1 monokloninis antikūnas, specifinis žmogaus interleukino-1 alfa - kolorektaliniai navikai - antinavikiniai vaistai - gydymo metastazavusiu kolorektaliniu vėžiu.
removab
neovii biotech gmbh - catumaxomab - ascites; cancer - kiti antineoplastiniai agentai - removab yra skirtas piktybinis ascitas pacientams, sergantiems epcam teigiamas karcinomos, kai standartinis gydymas nėra arba jie nebebus įmanoma į pilvą gydymui.
oxyglobin
opk biotech netherlands bv - hemoglobinas glutamer-200 (galvijų) - kraujo pakaitalai ir infuziniai tirpalai. - Šunys - oksiglobinas užtikrina deguonies palaikymą šunims, pagerinantiems klinikinius anemijos požymius mažiausiai 24 valandas, nepriklausomai nuo pagrindinės būklės.
tecfidera
biogen netherlands b.v. - dimetilfumaratas - išsėtinė sklerozė - imunosupresantai - tecfidera is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).
plegridy
biogen netherlands b.v. - peginterferonas beta-1a - išsėtinė sklerozė - immunostimulants, - suaugusiems pacientams gydant recidyvuojančią remituojančią išsėtinę sklerozę.
tysabri
biogen netherlands b.v. - natalizumabas - išsėtinė sklerozė - selektyvūs imunosupresantai - tysabri is indicated as single disease modifying therapy in adults with highly active relapsing remitting multiple sclerosis for the following patient groups: , patients with highly active disease activity despite a full and adequate course of treatment with at least one disease modifying therapy (dmt) (for exceptions and information about washout periods see sections 4. 4 ir 5. 1), , or, patients with rapidly evolving severe relapsing remitting multiple sclerosis defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain mri or a significant increase in t2 lesion load as compared to a previous recent mri.
spikevax (previously covid-19 vaccine moderna)
moderna biotech spain, s.l. - single-stranded, 5’-capped messenger rna (mrna) produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - vakcinos - spikevax is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older. spikevax bivalent original/omicron ba. 1 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 years of age and older who have previously received at least a primary vaccination course against covid-19. spikevax bivalent original/omicron ba. 4-5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older. spikevax xbb. 5 is indicated for active immunisation to prevent covid 19 caused by sars-cov-2 in individuals 6 months of age and older. the use of this vaccine should be in accordance with official recommendations.
cevenfacta
laboratoire francais du fractionnement et des biotechnologies - eptacog beta (activated) - hemophilia a; hemophilia b - antihemoraginiai - cevenfacta is indicated in adults and adolescents (12 years of age and older) for the treatment of bleeding episodes and for the prevention of bleeding in those undergoing surgery or invasive procedures in the following patient groups:in patients with congenital haemophilia with high-responding inhibitors to coagulation factors viii or ix (i. ≥5 bethesda units (bu)); in patients with congenital haemophilia with low titre inhibitors (bu.
atryn
laboratoire francais du fractionnement et des biotechnologies - antithrombin alfa - antitrombino iii trūkumas - antitromboziniai vaistai - atryn skiriamas venų tromboembolijos profilaktikai pacientams, kuriems yra įgimtas antitrombino trūkumas. atryn paprastai skiriamas kartu su heparinu arba mažos molekulinės masės heparinu.