Eiropas Savienība - latviešu - EMA (European Medicines Agency)

roche registration gmbh - polatuzumab vedotin - limfomas b-Šūnu - antineoplastiski līdzekļi - polivy kopā ar bendamustine un rituksimabs ir norādīts ārstēšanai pieaugušiem pacientiem ar relapsed/ugunsizturīgi difūza liela b-šūnu limfoma (dlbcl), kas nav kandidātu hematopoētisko cilmes šūnu transplantācijas. polivy in combination with rituximab, cyclophosphamide, doxorubicin, and prednisone (r-chp) is indicated for the treatment of adult patients with previously untreated diffuse large b-cell lymphoma (dlbcl).

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

janssen-cilag international nv - ibrutinibs - lymphoma, mantle-cell; leukemia, lymphocytic, chronic, b-cell - antineoplastic agents, protein kinase inhibitors - imbruvica as a single agent is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (mcl). imbruvica as a single agent or in combination with rituximab or obinutuzumab or venetoclax is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll) (see section 5. imbruvica as a single agent or in combination with bendamustine and rituximab (br) is indicated for the treatment of adult patients with cll who have received at least one prior therapy. imbruvica as a single agent is indicated for the treatment of adult patients with waldenström’s macroglobulinaemia (wm) who have received at least one prior therapy, or in first line treatment for patients unsuitable for chemo immunotherapy. imbruvica in combination with rituximab is indicated for the treatment of adult patients with wm.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

tesaro bio netherlands b.v. - rolipants - vomiting; nausea; cancer - pretvemšanas un antinauseants, - aizkavēta slikta dūša un vemšana, kas saistīta ar augstu un mēreni emetogēnu vēža ķīmijterapiju, pieaugušajiem. varuby tiek dota, kā daļu no terapijas kombinācija.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

novartis europharm limited - tisagenlecleucel - precursor b-cell lymphoblastic leukemia-lymphoma; lymphoma, large b-cell, diffuse - other antineoplastic agents - kymriah is indicated for the treatment of:• paediatric and young adult patients up to and including 25 years of age with b cell acute lymphoblastic leukaemia (all) that is refractory, in relapse post transplant or in second or later relapse. • adult patients with relapsed or refractory diffuse large b cell lymphoma (dlbcl) after two or more lines of systemic therapy. • adult patients with relapsed or refractory follicular lymphoma (fl) after two or more lines of systemic therapy.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

celltrion healthcare hungary kft. - rituximab - lymphoma, non-hodgkin; microscopic polyangiitis; leukemia, lymphocytic, chronic, b-cell; wegener granulomatosis - antineoplastiski līdzekļi - rituzena ir norādīts pieaugušos par šādām norādēm:ne-hodžkina limfoma (nhl)rituzena ir indicēts, lai ārstētu iepriekš neārstētiem pacientiem ar iii stadija iv folikulu limfomas kombinācijā ar ķīmijterapiju. rituzena monotherapy ir norādīts ārstēšanai pacientiem ar iii stadija iv folikulu limfomu, kas ir chemo izturīgs vai ir to otro vai nākamo recidīva pēc ķīmijterapijas. rituzena ir indicēts, lai ārstētu pacientus ar cd20 pozitīva difūza liela b šūnu ne hodžkina limfomas kombinācijā ar chop (ciklofosfamīdu, doksorubicīna, vincristine, prednizolons) ķīmijterapija. hroniskas limfocītu leikēmija (cll)rituzena kombinācijā ar ķīmijterapiju, ir indicēts, lai ārstētu pacientus ar iepriekš neārstētiem un relapsed/ugunsizturīgi cll. ir pieejami visai ierobežoti dati par efektivitāti un drošību pacientiem, kas iepriekš ārstēti ar monoklonālo antivielu tostarp rituzenaor pacientiem, ugunsizturīgas, lai iepriekšējā rituzena plus ķīmijterapiju. granulomatosis ar polyangiitis un mikroskopisko polyangiitisrituzena, kopā ar glucocorticoids, ir norādīts uz indukcijas atlaišanu pieaugušiem pacientiem ar smagu, aktīvu granulomatosis ar polyangiitis (wegener) (gpa) un mikroskopisko polyangiitis (mpa).

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

beigene ireland ltd - zanubrutinib - waldenstrom macroglobulinemia - antineoplastiski līdzekļi - brukinsa as monotherapy is indicated for the treatment of adult patients with waldenström’s macroglobulinaemia (wm) who have received at least one prior therapy, or in first line treatment for patients unsuitable for chemo-immunotherapy. brukinsa as monotherapy is indicated for the treatment of adult patients with marginal zone lymphoma (mzl) who have received at least one prior anti-cd20-based therapy. brukinsa as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukemia (cll).

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

abbvie deutschland gmbh co. kg - venetoklakss - leikēmija, limfocītu, hroniska, b-šūna - antineoplastiski līdzekļi - venclyxto in combination with obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll) (see section 5. venclyxto in combination with rituximab is indicated for the treatment of adult patients with cll who have received at least one prior therapy. venclyxto monotherapy is indicated for the treatment of cll:- in the presence of 17p deletion or tp53 mutation in adult patients who are unsuitable for or have failed a b cell receptor pathway inhibitor, or- in the absence of 17p deletion or tp53 mutation in adult patients who have failed both chemoimmunotherapy and a b-cell receptor pathway inhibitor. venclyxto in combination with a hypomethylating agent is indicated for the treatment of adult patients with newly  diagnosed acute myeloid leukaemia (aml) who are ineligible for intensive chemotherapy.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

astrazeneca ab - acalabrutinib - leikēmija, limfocītu, hroniska, b-šūna - antineoplastic agents, protein kinase inhibitors, - calquence as monotherapy or in combination with obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll). calquence as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukaemia (cll) who have received at least one prior therapy.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

incyte biosciences distribution b.v. - tafasitamab - lymphoma, large b-cell, diffuse - antineoplastiski līdzekļi - minjuvi is indicated in combination with lenalidomide followed by minjuvi monotherapy for the treatment of adult patients with relapsed or refractory diffuse large b-cell lymphoma (dlbcl) who are not eligible for autologous stem cell transplant (asct).