Fulvestrant medac 250 mg injektioneste, liuos, esitäytetty ruisku Suomi - suomi - Fimea (Suomen lääkevirasto)

fulvestrant medac 250 mg injektioneste, liuos, esitäytetty ruisku

medac gesellschaft fÜr klinische spezialprÄparate mbh - fulvestrant - injektioneste, liuos, esitäytetty ruisku - 250 mg - fulvestrantti

Fulvestrant Reddy 250 mg injektioneste, liuos, esitäytetty ruisku Suomi - suomi - Fimea (Suomen lääkevirasto)

fulvestrant reddy 250 mg injektioneste, liuos, esitäytetty ruisku

reddy holding gmbh - fulvestrant - injektioneste, liuos, esitäytetty ruisku - 250 mg - fulvestrantti

Fulvestrant Mylan Euroopan unioni - suomi - EMA (European Medicines Agency)

fulvestrant mylan

mylan pharmaceuticals limited - fulvestrantti - rintojen kasvaimet - endokriinihoito - fulvestrantti on tarkoitettu hoitoon estrogeenin reseptorin positiivinen, paikallisesti edenneen tai metastasoituneen rintasyövän hoidossa vaihdevuodet ohittaneille naisille:ei ole aiemmin käsitelty hormonaalisen hoidon, tai taudin uusiutumisen tai sen jälkeen adjuvanttia anti-estrogeeni hoidon tai taudin etenemistä on antiestrogeeni hoito.

Verzenios Euroopan unioni - suomi - EMA (European Medicines Agency)

verzenios

eli lilly nederland b.v. - abemaciclib - rintojen kasvaimet - antineoplastiset aineet - early breast cancerverzenios in combination with endocrine therapy is indicated for the adjuvant treatment of adult patients with hormone receptor (hr) positive, human epidermal growth factor receptor 2 (her2) negative, node positive early breast cancer at high risk of recurrence (see section 5. in pre or perimenopausal women, aromatase inhibitor endocrine therapy should be combined with a luteinising hormone-releasing hormone (lhrh) agonist. advanced or metastatic breast cancerverzenios is indicated for the treatment of women with hormone receptor (hr) positive, human epidermal growth factor receptor 2 (her2) negative locally advanced or metastatic breast cancer in combination with an aromatase inhibitor or fulvestrant as initial endocrine-based therapy, or in women who have received prior endocrine therapy. in pre- or perimenopausal women, the endocrine therapy should be combined with a lhrh agonist.

Phesgo Euroopan unioni - suomi - EMA (European Medicines Agency)

phesgo

roche registration gmbh - pertuzumab, trastuzumab - rintojen kasvaimet - antineoplastiset aineet - early breast cancer (ebc)phesgo is indicated for use in combination with chemotherapy in:the neoadjuvant treatment of adult patients with her2-positive, locally advanced, inflammatory, or early stage breast cancer at high risk of recurrencethe adjuvant treatment of adult patients with her2-positive early breast cancer at high risk of recurrencemetastatic breast cancer (mbc)phesgo is indicated for use in combination with docetaxel in adult patients with her2-positive metastatic or locally recurrent unresectable breast cancer, who have not received previous anti-her2 therapy or chemotherapy for their metastatic disease.