Verzenios الاتحاد الأوروبي - السلوفاكية - EMA (European Medicines Agency)

verzenios

eli lilly nederland b.v. - abemaciclib - neoplazmy prsníkov - antineoplastické činidlá - 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.

Baqsimi الاتحاد الأوروبي - السلوفاكية - EMA (European Medicines Agency)

baqsimi

eli lilly nederland b.v. - glukagónu - cukrovka - pankreatických hormónov, glycogenolytic hormóny - baqsimi je indikovaný na liečbu ťažkú hypoglykémiu u dospelých, dospievajúcich a detí vo veku 4 rokov a viac s diabetes mellitus.

Retsevmo الاتحاد الأوروبي - السلوفاكية - EMA (European Medicines Agency)

retsevmo

eli lilly nederland b.v. - selpercatinib - carcinoma, non-small-cell lung; thyroid neoplasms - antineoplastické činidlá - retsevmo as monotherapy is indicated for the treatment of adults and adolescents 12 years and older with advanced ret-mutant medullary thyroid cancer (mtc)advanced ret fusion-positive non-small cell lung cancer (nsclc) not previously treated with a ret inhibitoradvanced ret fusion-positive thyroid cancer who require systematic therapy following prior treatment.

Omvoh الاتحاد الأوروبي - السلوفاكية - EMA (European Medicines Agency)

omvoh

eli lilly nederland b.v. - mirikizumab - kolitída, ulceratívna - imunosupresíva - omvoh is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a biologic treatment.

Jaypirca الاتحاد الأوروبي - السلوفاكية - EMA (European Medicines Agency)

jaypirca

eli lilly nederland b.v. - pirtobrutinib - lymfóm, mantle-cell - protein kinase inhibítory - treatment of mantle cell lymphoma (mcl).

Xagrid الاتحاد الأوروبي - السلوفاكية - EMA (European Medicines Agency)

xagrid

takeda pharmaceuticals international ag ireland branch - anagrelide - trombocytémia, esenciálna - antineoplastické činidlá - xagrid je indikovaný na redukciu zvýšeného počtu krvných doštičiek v rizikových esenciálne-polycytémii vera (et) pacientov, ktorí sú intolerantní k ich súčasnej liečbe alebo ktorých zvýšený počet krvných doštičiek sú nie znížiť na prijateľnú úroveň prostredníctvom ich aktuálnej terapii. at-risk patientan at-risk et je definovaný jeden alebo viac z nasledujúcich funkcií:>60 rokov veku alebo;a krvných doštičiek >1000 x 109/l alebo;dejiny thrombohaemorrhagic udalosti.