Evropska unija - slovenščina - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - deksametazon - macular edema; uveitis - ophthalmologicals, other ophthalmologicals - ozurdex je indiciran za zdravljenje odraslih bolnikov z degeneracijo edem naslednje bodisi podružnico mrežnice-vene (brvo) ali centralne mrežnice-vene (crvo). ozurdex je indiciran za zdravljenje odraslih bolnikov z vnetjem zadnji segment očesa, ki predstavljajo, kot noninfectious uveitis. ozurdex je indiciran za zdravljenje odraslih bolnikov s vida zaradi diabetično degeneracija edem (dme), ki so pseudophakic ali, ki so ovrednotena dovolj odziven, ali neprimerne za ne-kortikosteroidne terapije.

Evropska unija - slovenščina - EMA (European Medicines Agency)

janssen-cilag international n.v. - daratumumab - multiple myeloma - monoclonal antibodies and antibody drug conjugates, antineoplastic agents - multiple myelomadarzalex is indicated: in combination with lenalidomide and dexamethasone or with bortezomib, melphalan and prednisone for the treatment of adult patients with newly diagnosed multiple myeloma who are ineligible for autologous stem cell transplant. v kombinaciji z bortezomib, thalidomide in dexamethasone za zdravljenje odraslih bolnikov z na novo prijavljenih več plazmocitom, ki so upravičeni do autologous matičnih celic za presajanje. v kombinaciji z lenalidomide in dexamethasone, ali bortezomib in dexamethasone, za zdravljenje odraslih bolnikov z več plazmocitom, ki so prejeli vsaj en pred terapijo. in combination with pomalidomide and dexamethasone for the treatment of adult patients with multiple myeloma who have received one prior therapy containing a proteasome inhibitor and lenalidomide and were lenalidomide refractory, or who have received at least two prior therapies that included lenalidomide and a proteasome inhibitor and have demonstrated disease progression on or after the last therapy (see section 5. kot monotherapy za zdravljenje odraslih bolnikov z relapsed in ognjevzdržne več plazmocitom, katerih predhodno zdravljenje vključeni proteasome serotonina in imunomodulatornimi agent in ki so pokazali napredovanja bolezni na zadnji terapija. al amyloidosisdarzalex is indicated in combination with cyclophosphamide, bortezomib and dexamethasone for the treatment of adult patients with newly diagnosed systemic light chain (al) amyloidosis.

Evropska unija - slovenščina - EMA (European Medicines Agency)

mylan ireland limited - lenalidomid - multiple myeloma - imunosupresivi - multiple myelomalenalidomide mylan as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide mylan as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone is indicated for the treatment of adult patients with previously untreated multiple myeloma who are not eligible for transplant. lenalidomide mylan in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. follicular lymphomalenalidomide mylan in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1-3a).

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

deksametazon - peroralna raztopina - deksametazon 1 mg / 1 ml - deksametazon

Evropska unija - slovenščina - EMA (European Medicines Agency)

sanofi winthrop industrie - isatuximab - multiple myeloma - antineoplastična sredstva - sarclisa is indicated: in combination with pomalidomide and dexamethasone, for the treatment of adult patients with relapsed and refractory multiple myeloma (mm) who have received at least two prior therapies including lenalidomide and a proteasome inhibitor (pi) and have demonstrated disease progression on the last therapy. in combination with carfilzomib and dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least one prior therapy (see section 5.

Evropska unija - slovenščina - EMA (European Medicines Agency)

theravia - deksametazon - multiple myeloma - kortikosteroidi za sistemsko uporabo - zdravljenje večkratnega mieloma.

Evropska unija - slovenščina - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - pomalidomide - multiple myeloma - imunosupresivi - imnovid v kombinaciji z bortezomib in dexamethasone je indiciran za zdravljenje odraslih bolnikov z več plazmocitom, ki so prejeli vsaj eno predhodno zdravljenje režim, vključno z lenalidomide. imnovid v kombinaciji z deksametazon je indicirano za zdravljenje odraslih bolnikov s ponovila in ognjevarnih multipli mielom, ki so prejeli vsaj dve režimi predhodne obdelave, vključno s lenalidomid in bortezomib, in so pokazali napredovanje bolezni na zadnje terapije.

Evropska unija - slovenščina - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - lenalidomid - multiple myeloma; lymphoma, mantle-cell; myelodysplastic syndromes - imunosupresivi - več myelomarevlimid kot monotherapy je označen za vzdrževanje zdravljenje odraslih bolnikov z na novo prijavljenih več plazmocitom, ki so bili autologous presaditev matičnih celic. revlimid kot kombinacija terapije z dexamethasone, ali bortezomib in dexamethasone, ali melphalan in prednizon (glej poglavje 4. 2) je indiciran za zdravljenje odraslih bolnikov s predhodno nezdravljenih več plazmocitom, ki niso primerni za presaditev. revlimid v kombinaciji z dexamethasone je primerna za zdravljenje več plazmocitom pri odraslih bolnikih, ki so prejeli vsaj en pred terapijo. myelodysplastic syndromesrevlimid kot monotherapy je indiciran za zdravljenje odraslih bolnikov s transfuzijo-odvisne anemije zaradi nizko - ali vmesne-1-tveganje myelodysplastic sindromov, povezanih z osamljen izbris 5q postopek citogenetske nepravilnosti pri drugih terapevtskih možnosti so nezadostna ali neustrezna. plašč celice lymphomarevlimid kot monotherapy je indiciran za zdravljenje odraslih bolnikov z relapsed ali ognjevzdržni plašč limfom celic. folikularni lymphomarevlimid v kombinaciji z rituksimabom (anti-cd20 protiteles) je indiciran za zdravljenje odraslih bolnikov s predhodno zdravljenih folikularni limfom (razred 1 – 3a).

Evropska unija - slovenščina - EMA (European Medicines Agency)

janssen-cilag international nv - bortezomib - multiple myeloma - antineoplastična sredstva - velcade kot monoterapijo ali v kombinaciji z interferonom liposomski doksorubicinijev ali deksametazon je indiciran za zdravljenje odraslih bolnikov s postopno multipli mielom, ki so prejeli vsaj 1 predhodno terapijo in ki so že bili ali so neprimerna za presaditve krvotvornih matičnih celic. velcade v kombinaciji z melphalan in prednizon je indiciran za zdravljenje odraslih bolnikov s predhodno nezdravljenih več plazmocitom, ki ne izpolnjujejo pogojev za visok odmerek kemoterapijo z haematopoietic stem cell presaditev. velcade v kombinaciji z dexamethasone, ali z dexamethasone in thalidomide, je primerna za indukcijsko zdravljenje odraslih bolnikov s predhodno nezdravljenih več plazmocitom, ki so upravičeni za visok odmerek kemoterapijo z haematopoietic stem cell presaditev. velcade v kombinaciji z rituksimabom, ciklofosfamid, doxorubicin in prednizon je indiciran za zdravljenje odraslih bolnikov s predhodno nezdravljenih plašč limfom celic, ki so neprimerni za haematopoietic stem cell presaditev.

Evropska unija - slovenščina - EMA (European Medicines Agency)

krka, d.d., novo mesto  - lenalidomide hydrochloride monohydrate - multiple myeloma; lymphoma, follicular - imunosupresivi - multiple myelomalenalidomide krka d. novo mesto 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. novo mesto as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) je indiciran za zdravljenje odraslih bolnikov s predhodno nezdravljenih več plazmocitom, ki niso primerni za presaditev. lenalidomide krka d. novo mesto in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. follicular lymphomalenalidomide krka d. novo mesto in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a). multiple myelomalenalidomide krka d. novo mesto 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. novo mesto as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) je indiciran za zdravljenje odraslih bolnikov s predhodno nezdravljenih več plazmocitom, ki niso primerni za presaditev. lenalidomide krka d. novo mesto in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. follicular lymphomalenalidomide krka d. novo mesto in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a).