TENLORIS õhukese polümeerikattega tablett Estonia - Esti - Ravimiamet

tenloris õhukese polümeerikattega tablett

krka, d.d., novo mesto - losartaan+amlodipiin - õhukese polümeerikattega tablett - 50mg+5mg 10tk; 50mg+5mg 60tk; 50mg+5mg 56tk; 50mg+5mg 28tk; 50mg+5mg 84tk

OXYCODONE KALCEKS süste-/infusioonilahus Estonia - Esti - Ravimiamet

oxycodone kalceks süste-/infusioonilahus

kalceks as - oksükodoon - süste-/infusioonilahus - 50mg 1ml 1ml 5tk

OXYCODONE KALCEKS süste-/infusioonilahus Estonia - Esti - Ravimiamet

oxycodone kalceks süste-/infusioonilahus

kalceks as - oksükodoon - süste-/infusioonilahus - 10mg 1ml 1ml 5tk; 10mg 1ml 2ml 5tk; 10mg 1ml 1ml 25tk; 10mg 1ml 2ml 10tk; 10mg 1ml 1ml 10tk

TENLORIS õhukese polümeerikattega tablett Estonia - Esti - Ravimiamet

tenloris õhukese polümeerikattega tablett

krka, d.d., novo mesto - losartaan+amlodipiin - õhukese polümeerikattega tablett - 50mg+10mg 84tk; 50mg+10mg 28tk; 50mg+10mg 10tk; 50mg+10mg 30tk; 50mg+10mg 56tk

TENLORIS õhukese polümeerikattega tablett Estonia - Esti - Ravimiamet

tenloris õhukese polümeerikattega tablett

krka, d.d., novo mesto - losartaan+amlodipiin - õhukese polümeerikattega tablett - 100mg+5mg 84tk; 100mg+5mg 90tk; 100mg+5mg 30tk; 100mg+5mg 60tk

TENLORIS õhukese polümeerikattega tablett Estonia - Esti - Ravimiamet

tenloris õhukese polümeerikattega tablett

krka, d.d., novo mesto - losartaan+amlodipiin - õhukese polümeerikattega tablett - 100mg+10mg 30tk; 100mg+10mg 90tk; 100mg+10mg 56tk; 100mg+10mg 60tk

FLUDARABINE KABI 50 MG süste-/infusioonilahuse pulber Estonia - Esti - Ravimiamet

fludarabine kabi 50 mg süste-/infusioonilahuse pulber

fresenius kabi oncology plc - fludarabiin - süste-/infusioonilahuse pulber - 50mg 50mg 1tk

Vaxzevria (previously COVID-19 Vaccine AstraZeneca) Uni Eropa - Esti - EMA (European Medicines Agency)

vaxzevria (previously covid-19 vaccine astrazeneca)

astrazeneca ab - chadox1-sars-cov-2 - covid-19 virus infection - vaktsiinid - vaxzevria is indicated for active immunisation to prevent covid 19 caused by sars cov 2, in individuals 18 years of age and older. kasutamist see vaktsiin peaks olema kooskõlas ametlike soovitustega.

Blincyto Uni Eropa - Esti - EMA (European Medicines Agency)

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.

Columvi Uni Eropa - Esti - EMA (European Medicines Agency)

columvi

roche registration gmbh  - glofitamab - lymphoma, large b-cell, diffuse - antineoplastilised ained - columvi as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large b cell lymphoma (dlbcl), after two or more lines of systemic therapy.