Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

janssen-cilag ag - ibrutinibum - kapseln - ibrutinibum 140 mg, cellulosum microcristallinum, carmellosum natricum conexum, natrii laurilsulfas, magnesii stearas, kapselhülle: gelatina, e 171, drucktinte: lacca, e 172, propylenglycolum, pro capsula corresp. natrium 2.73 mg. - mantelzelllymphom, chronische lymphatische leukämie, morbus waldenström - synthetika

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

janssen-cilag ag - ibrutinibum - filmtabletten - ibrutinibum 140 mg, lactosum monohydricum 28 mg, carmellosum natricum conexum, natrii laurilsulfas, povidonum k 25, cellulosum microcristallinum, silica colloidalis anhydrica, magnesii stearas, Überzug: poly(alcohol vinylicus), macrogolum, talcum, e 171, e 172, pro compresso obducto corresp. natrium 1.14 mg. - mantelzelllymphom, chronische lymphatische leukämie, morbus waldenström - synthetika

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

janssen-cilag ag - ibrutinibum - filmtabletten - ibrutinibum 280 mg, lactosum monohydricum 56 mg, carmellosum natricum conexum, natrii laurilsulfas, povidonum k 25, cellulosum microcristallinum, silica colloidalis anhydrica, magnesii stearas, Überzug: poly(alcohol vinylicus), macrogolum, talcum, e 171, e 172, pro compresso obducto corresp., natrium 2.28 mg. - mantelzelllymphom, chronische lymphatische leukämie, morbus waldenström - synthetika

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

janssen-cilag ag - ibrutinibum - filmtabletten - ibrutinibum 420 mg, lactosum monohydricum 84 mg, carmellosum natricum conexum, natrii laurilsulfas, povidonum k 25, cellulosum microcristallinum, silica colloidalis anhydrica, magnesii stearas, Überzug: poly(alcohol vinylicus), macrogolum, talcum, e 171, e 172, pro compresso obducto corresp. natrium 3.42 mg. - mantelzelllymphom, chronische lymphatische leukämie, morbus waldenström - synthetika

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

janssen-cilag ag - ibrutinibum - filmtabletten - ibrutinibum 560 mg, lactosum monohydricum 112 mg, carmellosum natricum conexum, natrii laurilsulfas, povidonum k 25, cellulosum microcristallinum, silica colloidalis anhydrica, magnesii stearas, Überzug: poly(alcohol vinylicus), macrogolum, talcum, e 171, e 172, pro compresso obducto corresp. natrium 4.56 mg. - mantelzelllymphom, chronische lymphatische leukämie, morbus waldenström - synthetika

Europäische Union - Deutsch - EMA (European Medicines Agency)

secura bio limited - duvelisib - leukemia, lymphocytic, chronic, b-cell; lymphoma, follicular - antineoplastische mittel - 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.

Europäische Union - Deutsch - EMA (European Medicines Agency)

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.

Deutschland - Deutsch - BfArM (Bundesinstitut für Arzneimittel und Medizinprodukte)

zr pharma& gmbh - zweigniederlassung hietzing - (1009897) - bendamustinhydrochlorid - pulver für ein konzentrat zur herstellung einer infusionslösung - teil 1 - pulver für ein konzentrat zur herstellung einer infusionslösung; bendamustinhydrochlorid (36755) 2,5 milligramm

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

janssen-cilag ag - daratumumabum - konzentrat zur herstellung einer infusionslösung - daratumumabum 100 mg, acidum aceticum glaciale, natrii acetas trihydricus, natrii chloridum, mannitolum, polysorbatum 20, aqua ad iniectabile q.s. ad solutionem pro 5 ml corresp. natrium 9.4 mg. - multiples myelom - biotechnologika

Schweiz - Deutsch - Swissmedic (Swiss Agency for Therapeutic Products)

janssen-cilag ag - daratumumabum - konzentrat zur herstellung einer infusionslösung - daratumumabum 400 mg, acidum aceticum glaciale, natrii acetas trihydricus, natrii chloridum, mannitolum, polysorbatum 20, aqua ad iniectabile q.s. ad solutionem pro 20 ml corresp. natrium 37.7 mg. - multiples myelom - biotechnologika