Lenalidomide Krka d.d. Európska únia - estónčina - EMA (European Medicines Agency)

lenalidomide krka d.d.

krka, d.d., novo mesto  - lenalidomide hydrochloride hydrate - multiple myeloma; lymphoma, follicular; myelodysplastic syndromes - immunosupressandid - multiple myelomalenalidomide krka d. as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide krka d. as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) on näidustatud ravi täiskasvanud patsientidel, kellel on varem ravimata hulgimüeloom, kes ei ole abikõlblikud siirdamist. lenalidomide krka d. in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. myelodysplastic syndromeslenalidomide krka d. as monotherapy is indicated for the treatment of adult patients with transfusion-dependent anemia due to low- or intermediate-1-risk myelodysplastic syndromes associated with an isolated deletion 5q cytogenetic abnormality when other therapeutic options are insufficient or inadequate. follicular lymphomalenalidomide krka d. in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a).

Dexafort süstesuspensioon Estónsko - estónčina - Ravimiamet

dexafort süstesuspensioon

vet pharma friesoythe gmbh - deksametasoon - süstesuspensioon - 3mg 1ml 50ml 1tk

Nexpovio Európska únia - estónčina - EMA (European Medicines Agency)

nexpovio

stemline therapeutics b.v. - selinexor - mitu müeloomit - antineoplastilised ained - nexpovio is indicatedin combination with bortezomib and dexamethasone for the treatment of adult patients with multiple myeloma who have received at least one prior therapy. in combination with dexamethasone for the treatment of multiple myeloma in adult patients who have received at least four prior therapies and whose disease is refractory to at least two proteasome inhibitors, two immunomodulatory agents and an anti-cd38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.

Dexavet silmatilgad, lahus Estónsko - estónčina - Ravimiamet

dexavet silmatilgad, lahus

cp-pharma handelsgesellschaft mbh - deksametasoon - silmatilgad, lahus - 1mg 1ml 5ml 1tk

Cefenidex silmatilgad, lahus Estónsko - estónčina - Ravimiamet

cefenidex silmatilgad, lahus

cp-pharma handelsgesellschaft mbh - deksametasoon+klooramfenikool - silmatilgad, lahus - 1mg+2mg 1ml 10ml 1tk

Zynlonta Európska únia - estónčina - EMA (European Medicines Agency)

zynlonta

swedish orphan biovitrum ab - loncastuximab tesirine - lymphoma, large b-cell, diffuse; lymphoma, b-cell - antineoplastilised ained - zynlonta as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large b-cell lymphoma (dlbcl) and high-grade b-cell lymphoma (hgbl), after two or more lines of systemic therapy.

Dexavet silmasalv Estónsko - estónčina - Ravimiamet

dexavet silmasalv

cp-pharma handelsgesellschaft mbh - deksametasoon - silmasalv - 1mg 1g 5g 1tk

ONDANSETRON BAXTER süstelahus Estónsko - estónčina - Ravimiamet

ondansetron baxter süstelahus

baxter holding b.v. - ondansetroon - süstelahus - 2mg 1ml 2ml 25tk; 2mg 1ml 2ml 5tk; 2mg 1ml 4ml 25tk; 2mg 1ml 4ml 5tk

ONDANSETRON KALCEKS süste-/infusioonilahus Estónsko - estónčina - Ravimiamet

ondansetron kalceks süste-/infusioonilahus

kalceks as - ondansetroon - süste-/infusioonilahus - 2mg 1ml 2ml 25tk; 2mg 1ml 2ml 10tk; 2mg 1ml 2ml 5tk; 2mg 1ml 4ml 10tk

Alimta Európska únia - estónčina - EMA (European Medicines Agency)

alimta

eli lilly nederland b.v. - pemetrekseed - mesothelioma; carcinoma, non-small-cell lung - antineoplastilised ained - pleura pahaloomulise mesotheliomaalimta koos cisplatin on näidustatud ravi keemiaravi-naiivne patsientidel unresectable pleura pahaloomulise mesotelioomi. non-small-cell lung canceralimta koos cisplatin on näidustatud esimese rea raviks patsientidel, kellel on lokaalselt kaugelearenenud või metastaatilise mitte-small-cell lung cancer, v.a peamiselt soomusrakuline rakkude histoloogia. alimta on näidustatud monotherapy hooldus-ravi lokaalselt kaugelearenenud või metastaatilise mitte-small-cell lung cancer, v.a peamiselt soomusrakuline rakkude histoloogia patsientidel, kelle haigus ei ole jõudnud kohe pärast plaatina-põhinevat keemiaravi. alimta on näidustatud monotherapy teise rea ravi patsientidel, kellel on lokaalselt kaugelearenenud või metastaatilise mitte-small-cell lung cancer, v.a peamiselt soomusrakuline rakkude histoloogia.