Unione Europea - italiano - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - niraparib (tosilate monohydrate) - fallopian tube neoplasms; peritoneal neoplasms; ovarian neoplasms - agenti antineoplastici - zejula is indicated: , as monotherapy for the maintenance treatment of adult patients with advanced epithelial (figo stages iii and iv) high-grade ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy. , as monotherapy for the maintenance treatment of adult patients with platinum sensitive relapsed high grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) to platinum based chemotherapy.

Unione Europea - italiano - EMA (European Medicines Agency)

janssen-cilag international n.v. - abiraterone acetate, niraparib tosilate monohydrate - prostatica neoplasie, castrazione-resistente - agenti antineoplastici - treatment of adult patients with prostate cancer.

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

glaxosmithkline ag - niraparibum - capsule - kapsel: niraparibum 100 mg a niraparibi tosilas monohydricus, colore.: e 133, e 127, e 102, excipiens per la capsula. - onkologikum - synthetika

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

glaxosmithkline ag - niraparibum - compresse rivestite con film - niraparibum 100 mg ut niraparibi tosilas monohydricus, cellulosum microcristallinum, lactosum monohydricum 34.66 mg, povidonum k 30, crospovidonum, silica colloidalis hydrica, magnesii stearas, Überzug: poly(alcohol vinylicus), macrogolum 3350, talcum, e 171, e 172 (nigrum), pro compresso obducto. - onkologikum - synthetika

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

astrazeneca ag - olaparibum - compresse rivestite con film - olaparibum 100 mg, excipiens pro compresso obducto. - onkologikum - synthetika

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

astrazeneca ag - olaparibum - compresse rivestite con film - olaparibum 150 mg, excipiens pro compresso obducto. - onkologikum - synthetika

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

astrazeneca ag - olaparibum - capsule - olaparibum 50 mg, macrogolglyceridorum laurates, kapselhülle: hypromellosum, e 171, gellani gummi, kalii acetas, drucktinte: lacca, e 172 (nigrum), pro capsula. - onkologikum - synthetika

Unione Europea - italiano - EMA (European Medicines Agency)

astrazeneca ab - olaparib - neoplasie ovariche - agenti antineoplastici - ovarico cancerlynparza è indicato come monoterapia per il trattamento di mantenimento di pazienti adulti con avanzate (figo stadi iii e iv) brca1/2-mutato (germinale e/o somatica) di alta qualità epiteliali dell'ovaio, tube di falloppio o del cancro peritoneale primario che si trovano in risposta (completa o parziale) a seguito del completamento della prima linea di chemioterapia a base di platino. maintenance treatment of adult patients with platinum sensitive relapsed high grade epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) to platinum based chemotherapy. lynparza in combination with bevacizumab is indicated for the:maintenance treatment of adult patients with advanced (figo stages iii and iv) high-grade epithelial ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy in combination with bevacizumab and whose cancer is associated with homologous recombination deficiency (hrd) positive status defined by either a brca1/2 mutation and/or genomic instability (see section 5. breast cancerlynparza is indicated as:monotherapy or in combination with endocrine therapy for the adjuvant treatment of adult patients with germline brca1/2-mutations who have her2-negative, high risk early breast cancer previously treated with neoadjuvant or adjuvant chemotherapy (see sections 4. 2 e 5. monotherapy for the treatment of adult patients with germline brca1/2-mutations, who have her2 negative locally advanced or metastatic breast cancer. i pazienti devono essere stati precedentemente trattati con un'antraciclina e un taxano il (neo)adiuvante o metastatico impostazione a meno che i pazienti non erano adatti per questi trattamenti (vedere la sezione 5. i pazienti con recettore ormonale (hr)-positivo il cancro al seno dovrebbero avere fatto passi avanti o dopo la prima terapia endocrina, o essere considerati non idonei per la terapia endocrina. adenocarcinoma of the pancreaslynparza is indicated as:monotherapy for the maintenance treatment of adult patients with germline brca1/2-mutations who have metastatic adenocarcinoma of the pancreas and have not progressed after a minimum of 16 weeks of platinum treatment within a first-line chemotherapy regimen. prostate cancerlynparza is indicated as:monotherapy for the treatment of adult patients with metastatic castration-resistant prostate cancer (mcrpc) and brca1/2-mutations (germline and/or somatic) who have progressed following prior therapy that included a new hormonal agent. in combination with abiraterone and prednisone or prednisolone for the treatment of adult patients with mcrpc in whom chemotherapy is not clinically indicated (see section 5.

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

benedetti & co.spa - ramipril - compresse - "10 mg compresse" 28 compresse in blister pvdc/pvc/al

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

benedetti & co.spa - ramipril - compresse - "2,5 mg compresse" 28 compresse in blister pvdc/pvc/al