Natural Health Supply - Meklēšanas rezultāti

Eiropas Savienība - slovēņu - EMA (European Medicines Agency)

provenge

dendreon uk ltd - avtologni mononuklearnih celic periferne krvi, vključno z najmanj 50 milijonov avtologna cd54 + celice activated s prostate kisline fosfataze makrofagov granulocitne kolonije stimulirajoči faktor - prostatične neoplazme - drugi imunostimulanti - za zdravljenje asimptomatskega ali minimalno simptomatskega metastatskega (nestardalnega) kastratnega odpornega raka na prostati pri odraslih moških, pri katerem kemoterapija še ni klinično indicirana.

Eiropas Savienība - slovēņu - EMA (European Medicines Agency)

fasenra

astrazeneca ab - benralizumab - astma - zdravila za obstruktivne pljučne bolezni, - fasenra je indicirano kot dodatek na vzdrževanje zdravljenje pri odraslih bolnikih s hudo eozinofilno astmo neustrezno nadzorovano kljub visoki odmerki vdihavajo kortikosteroide plus dolgo delujoči beta agonistov.

Eiropas Savienība - slovēņu - EMA (European Medicines Agency)

abecma

bristol-myers squibb pharma eeig - idecabtagene vicleucel - multiple myeloma; neoplasms; cancer; neoplasms, plasma cell; hemostatic disorders; vascular diseases; cardiovascular diseases; paraproteinemias; blood protein disorders; hematologic diseases; hemic and lymphatic diseases; hemorrhagic disorders; infectious mononucleosis; lymphoproliferative disorders; immunoproliferative disorders; immune system diseases - antineoplastična sredstva - abecma is indicated 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.

Eiropas Savienība - slovēņu - EMA (European Medicines Agency)

carvykti

janssen-cilag international nv - ciltacabtagene autoleucel - multiple myeloma - carvykti is indicated 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.