Euroopa Liit - eesti - EMA (European Medicines Agency)

siga technologies netherlands b.v. - tecovirimat - poxviridae infections; cowpox; monkeypox; vaccinia; smallpox - viirusevastased ravimid süsteemseks kasutamiseks - tecovirimat siga is indicated for the treatment of the following viral infections in adults and children with body weight at least 13 kg:- smallpox- monkeypox- cowpoxtecovirimat siga is also indicated to treat complications due to replication of vaccinia virus following vaccination against smallpox in adults and children with body weight at least 13 kg (see sections 4. 4 ja 5. tecovirimat siga should be used in accordance with official recommendations.

Eesti - eesti - Ravimiamet

dr. august wolff gmbh & co. kg arzneimittel - glükopürroonium - kreem - 8mg 1g 50g 1tk

Euroopa Liit - eesti - EMA (European Medicines Agency)

janssen-cilag international n.v. - teclistamab - mitu müeloomit - antineoplastilised ained - tecvayli is indicated as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti-cd38 antibody and have demonstrated disease progression on the last therapy.

Eesti - eesti - Ravimiamet

sandoz pharmaceuticals d.d. - dabigatraaneteksilaat - kõvakapsel - 75mg 20tk; 75mg 10tk; 75mg 100tk

Eesti - eesti - Ravimiamet

sandoz pharmaceuticals d.d. - dabigatraaneteksilaat - kõvakapsel - 150mg 200tk

Eesti - eesti - Ravimiamet

sandoz pharmaceuticals d.d. - dabigatraaneteksilaat - kõvakapsel - 110mg 60tk; 110mg 30tk

Eesti - eesti - Ravimiamet

stada arzneimittel ag - dabigatraaneteksilaat - kõvakapsel - 110mg 100tk; 110mg 10tk; 110mg 60tk; 110mg 180tk; 110mg 30tk

Eesti - eesti - Ravimiamet

stada arzneimittel ag - dabigatraaneteksilaat - kõvakapsel - 75mg 30tk; 75mg 10tk

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.

Euroopa Liit - eesti - EMA (European Medicines Agency)

pfizer europe ma eeig - varenikliin - tubaka kasutamise lõpetamine - muud närvisüsteemi ravimid - champix on näidustatud suitsetamise lõpetamiseks täiskasvanutel.