Cotellic Unione Europea - bulgaro - EMA (European Medicines Agency)

cotellic

roche registration gmbh - кобиметиниб хемифумарат - Меланомът - Антинеопластични средства - cotellic е показан за употреба в комбинация с вемурафениб за лечение на възрастни пациенти с нерезекционна или метастатична меланома с braf v600 мутация.

Cresemba Unione Europea - bulgaro - EMA (European Medicines Agency)

cresemba

basilea pharmaceutica deutschland gmbh - isavuconazole - аспергилоза - cresemba е показан при възрастни за лечение на:инвазивни aspergillosismucormycosis при пациенти, за които амфотерицин В inappropriateconsideration трябва да се дава официални препоръки за правилното използване на противогъбични лекарства.

Exviera Unione Europea - bulgaro - EMA (European Medicines Agency)

exviera

abbvie ltd - дасабувир натрий - Хепатит c, хроничен - Антивирусни средства за системно приложение - exviera е показан в комбинация с други лекарствени продукти за лечение на хроничен хепатит С (chc) при възрастни. Вирусът на хепатит С (hcv) генотипа на определен вид дейност .

Iclusig Unione Europea - bulgaro - EMA (European Medicines Agency)

iclusig

incyte biosciences distribution b.v. - ponatinib - leukemia, myeloid; leukemia, lymphoid - antineoplastic agents, protein kinase inhibitors - iclusig is indicated in adult patients withchronic phase, accelerated phase, or blast phase chronic myeloid leukaemia (cml) who are resistant to dasatinib or nilotinib; who are intolerant to dasatinib or nilotinib and for whom subsequent treatment with imatinib is not clinically appropriate; or who have the t315i mutationphiladelphia chromosome positive acute lymphoblastic leukaemia (ph+ all) who are resistant to dasatinib; who are intolerant to dasatinib and for whom subsequent treatment with imatinib is not clinically appropriate; or who have the t315i mutation. Вижте раздели 4. 2 assessment of cardiovascular status prior to start of therapy and 4. 4 situations where an alternative treatment may be considered.

Imbruvica Unione Europea - bulgaro - EMA (European Medicines Agency)

imbruvica

janssen-cilag international nv - ibrutinib - 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.

Sivextro Unione Europea - bulgaro - EMA (European Medicines Agency)

sivextro

merck sharp & dohme b.v. - тедизолиден фосфат - soft tissue infections; skin diseases, bacterial - antibacterials for systemic use, , other antibacterials - sivextro is indicated for the treatment of acute bacterial skin and skin structure infections (absssi) in adults and adolescents 12 years of age and older.

Vyndaqel Unione Europea - bulgaro - EMA (European Medicines Agency)

vyndaqel

pfizer europe ma eeig - tafamidis - амилоидоза - Други лекарства в нервната система - vyndaqel е показан за лечение на транстиретиновата амилоидоза при възрастни пациенти със симптоматична полиневропатия с фаза 1 за забавяне на периферното неврологично увреждане.

Copiktra Unione Europea - bulgaro - EMA (European Medicines Agency)

copiktra

secura bio limited - duvelisib - leukemia, lymphocytic, chronic, b-cell; lymphoma, follicular - Антинеопластични средства - copiktra monotherapy is indicated for the treatment of adult patients with: relapsed or refractory chronic lymphocytic leukaemia (cll) after at least two prior therapies.  follicular lymphoma (fl) that is refractory to at least two prior  systemic therapies.

Artesunate Amivas Unione Europea - bulgaro - EMA (European Medicines Agency)

artesunate amivas

amivas ireland ltd - artesunate - малария - антипротозойни - artesunate amivas is indicated for the initial treatment of severe malaria in adults and children. Трябва да се вземат предвид официалните препоръки за правилното използване на малария агенти.

Brukinsa Unione Europea - bulgaro - EMA (European Medicines Agency)

brukinsa

beigene ireland ltd - zanubrutinib - waldenstrom macroglobulinemia - Антинеопластични средства - 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).