Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

janssen-cilag ag - abirateronum - compresse - abirateroni acetas 250 mg corresp. abirateronum 223 mg, lactosum monohydricum corresp. lactosum 188.72 mg, cellulosum microcristallinum, carmellosum natricum conexum et natrii laurilsulfas corresp. natrium 5.38 mg, povidonum k 29-32, silica colloidalis anhydrica, magnesii stearas, pro compresso. - prostatico - synthetika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

janssen-cilag ag - abirateronum - compresse rivestite con film - abirateroni acetas 500 mg corresp. abirateronum 446 mg, lactosum monohydricum corresp. lactosum 240.5 mg, carmellosum natricum conexum et natrii laurilsulfas corresp. natrium 10.42 mg, hypromellosum, cellulosum microcristallinum silicificatum, silica colloidalis anhydrica, magnesii stearas, Überzug: poly(alcohol vinylicus), macrogolum 3350, talcum, e 171, e 172 (rubrum), e 172 (nigrum), pro compresso obducto. - prostatico - synthetika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

spirig healthcare ag - abirateronum - compresse rivestite con film - abirateroni acetas 250.00 mg corresp. abirateronum 223 mg, carmellosum natricum conexum, natrii laurilsulfas, povidonum k 30, cellulosum microcristallinum, lactosum monohydricum 34.00 mg, silica colloidalis anhydrica, magnesii stearas, Überzug: poly(alcohol vinylicus), e 171, macrogolum 3350, talcum, pro compresso obducto corresp. natrium 5.3 mg. - prostatico - synthetika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

spirig healthcare ag - abirateronum - compresse rivestite con film - abirateroni acetas 500.00 mg corresp. abirateronum 446 mg, carmellosum natricum conexum, natrii laurilsulfas, povidonum k 30, cellulosum microcristallinum, lactosum monohydricum 68.00 mg, silica colloidalis anhydrica, magnesii stearas, Überzug: poly(alcohol vinylicus), e 171, macrogolum 3350, talcum, e 172 (rubrum), e 172 (nigrum), pro compresso obducto corresp. natrium 10.6 mg. - prostatico - synthetika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

accord healthcare ag - abirateronum - compresse rivestite con film - abirateroni acetas 500 mg corresp. abirateronum 446 mg, lactosum monohydricum 253.2 mg, cellulosum microcristallinum, carmellosum natricum conexum, hypromellosum, natrii laurilsulfas, silica colloidalis anhydrica, magnesii stearas, Überzug: poly(alcohol vinylicus), e 171, macrogolum 3350, talcum, e 172 (rubrum), e 172 (nigrum) pro compresso obducto corresp. natrium 12.24 mg. - prostatico - synthetika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

teva pharma ag - abirateronum - compresse rivestite con film - abirateroni acetas 500 mg corresp. abirateronum 446.0 mg, lactosum monohydricum 90 mg, natrii laurilsulfas, carmellosum natricum conexum, cellulosum microcristallinum, povidonum k 30, silica colloidalis anhydrica, magnesii stearas, Überzug: poly(alcohol vinylicus), e 171, macrogolum 3350, talcum, e 172 (flavum), pro compresso obducto corresp. natrium 9.96 mg. - prostatico - synthetika

Unione Europea - italiano - EMA (European Medicines Agency)

mylan ireland limited - abiraterone acetato - neoplasie prostatiche - endocrine therapy, other hormone antagonists and related agents - abiraterone mylan is indicated with prednisone or prednisolone for:the treatment of newly diagnosed high risk metastatic hormone sensitive prostate cancer (mhspc) in adult men in combination with androgen deprivation therapy (adt). the treatment of metastatic castration resistant prostate cancer (mcrpc) in adult men who are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy in whom chemotherapy is not yet clinically indicated. the treatment of mcrpc in adult men whose disease has progressed on or after a docetaxel based chemotherapy regimen.

Unione Europea - italiano - EMA (European Medicines Agency)

accord healthcare s.l.u. - abiraterone acetato - neoplasie prostatiche - terapia endocrina - abiraterone accord is indicated with prednisone or prednisolone for:the treatment of newly diagnosed high risk metastatic hormone sensitive prostate cancer (mhspc) in adult men in combination with androgen deprivation therapy (adt)the treatment of metastatic castration resistant prostate cancer (mcrpc) in adult men who are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy in whom chemotherapy is not yet clinically indicatedthe treatment of mcrpc in adult men whose disease has progressed on or after a docetaxel based chemotherapy regimen.

Unione Europea - italiano - EMA (European Medicines Agency)

krka, d.d., novo mesto - abiraterone acetato - neoplasie prostatiche - terapia endocrina - abiraterone krka is indicated with prednisone or prednisolone for:the treatment of newly diagnosed high risk metastatic hormone sensitive prostate cancer (mhspc) in adult men in combination with androgen deprivation therapy (adt) (see section 5. 1)the treatment of metastatic castration resistant prostate cancer (mcrpc) in adult men who are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy in whom chemotherapy is not yet clinically indicated (see section 5. 1)the treatment of mcrpc in adult men whose disease has progressed on or after a docetaxel-based chemotherapy regimen.

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

helvepharm ag - abirateroni acetas - compresse rivestite con film - abirateroni acetas 500 mg, lactosum monohydricum 253.20 mg, carmellosum natricum conexum, natrii laurilsulfas, hypromellosum, cellulosum microcristallinum silicificatum, silica colloidalis anhydrica, magnesii stearas, Überzug: poly(alcohol vinylicus), macrogolum 3350, talcum, e 171, e 172 (rubrum), e 172 (nigrum), pro compresso obducto corresp. natrium 11.984 mg. - prostatico - synthetika