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

verzenios

eli lilly nederland b.v. - abemaciclib - neoplasmata van de borst - antineoplastische middelen - 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.

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

retsevmo

eli lilly nederland b.v. - selpercatinib - carcinoma, non-small-cell lung; thyroid neoplasms - antineoplastische middelen - 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.

Mounjaro الاتحاد الأوروبي - الهولندية - EMA (European Medicines Agency)

mounjaro

eli lilly nederland b.v. - tirzepatide - diabetes mellitus, type 2 - geneesmiddelen die worden gebruikt bij diabetes - mounjaro is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise- as monotherapy when metformin is considered inappropriate due to intolerance or contraindications- in addition to other medicinal products for the treatment of diabetes. for study results with respect to combinations, effects on glycaemic control and the populations studied, see sections 4. 4, 4. 5 en 5.

Rayvow الاتحاد الأوروبي - الهولندية - EMA (European Medicines Agency)

rayvow

eli lilly nederland b.v. - lasmiditan succinate - migraine stoornissen - pijnstillers - rayvow is indicated for the acute treatment of the headache phase of migraine attacks, with or without aura in adults.

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

omvoh

eli lilly nederland b.v. - mirikizumab - colitis, ulcerative - immunosuppressiva - 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 - الهولندية - EMA (European Medicines Agency)

jaypirca

eli lilly nederland b.v. - pirtobrutinib - lymfoom, mantel-cel - proteïne kinase remmers - treatment of mantle cell lymphoma (mcl).

Trulicity الاتحاد الأوروبي - الهولندية - EMA (European Medicines Agency)

trulicity

eli lilly nederland b.v. - dulaglutide - diabetes mellitus, type 2 - drugs used in diabetes, blood glucose lowering drugs, excl. insulins - trulicity is indicated for the treatment of patients 10 years and above with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exerciseas monotherapy when metformin is considered inappropriate due to intolerance or contraindicationsin addition to other medicinal products for the treatment of diabetes. voor het onderzoek naar de resultaten met betrekking tot combinaties, effecten op de glycemische controle en cardiovasculaire gebeurtenissen, en de bestudeerde populaties, zie punt 4. 4, 4. 5 en 5.

Celiprolol HCL Teva 200 mg, filmomhulde tabletten هولندا - الهولندية - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

celiprolol hcl teva 200 mg, filmomhulde tabletten

teva nederland b.v. swensweg 5 2031 ga haarlem - celiprololhydrochloride 200 mg/stuk samenstelling overeenkomend met ; celiprolol 182,5 mg/stuk - filmomhulde tablet - cellulose, microkristallijn (e 460(i)) ; chinolinegeel aluminiumlak (e 104) ; croscarmellose natrium (e 468) ; dimeticon (e 900) ; hypromellose, type 2910 (3 - 15 mpa.s) (e 464) ; macrogol 6000 ; macrogolstearylether ; magnesiumstearaat (e 470b) ; mannitol (d-) (e 421) ; ponceau 4r aluminiumlak (e 124) ; siliciumdioxide, gehydrateerd (e 551) ; sorbinezuur (e 200) ; talk (e 553 b) ; titaandioxide (e 171), cellulose, microkristallijn (e 460) ; chinolinegeel aluminiumlak (e 104) ; croscarmellose natrium (e 468) ; dimeticon (e 900) ; hypromellose, type 2910 (3 - 15 mpa.s) (e 464) ; macrogol 6000 ; macrogolstearylether ; magnesiumstearaat (e 470b) ; mannitol (d-) (e 421) ; ponceau 4r aluminiumlak (e 124) ; siliciumdioxide, gehydrateerd (e 551) ; sorbinezuur (e 200) ; talk (e 553 b) ; titaandioxide (e 171), cellulose, microkristallijn (e 460) ; chinolinegeel (e 104) ; croscarmellose natrium (e 468) ; dimeticon (e 900) ; hypromellose (e 464) ; macrogolstearylether ; magnesiumstearaat (e 470b) ; mannitol (d-) (e 421) ; polyethyleenglycol (e 1521) ; ponceau 4r (e 124) ; silica, hydrate form unknown (e 551) ; silicone antifoam emulsion se 2 {mixture of 5 ingredients of which 4 solid} (ri) ; sorbinezuur (e 200) ; talk (e 553 b) ; titaandioxide (e 171), - celiprolol

Ganirelix Gedeon Richter الاتحاد الأوروبي - الهولندية - EMA (European Medicines Agency)

ganirelix gedeon richter

chemical works of gedeon richter plc. (gedeon richter plc.) - ganirelix acetate - reproductive techniques, assisted; ovulation induction; infertility, female - hypofyse en hypothalamische hormonen en analogen - prevention of premature luteinising hormone (lh) surges in women undergoing controlled ovarian hyperstimulation (coh) for assisted reproduction techniques (art).

Artuvetrin - test epithelia هولندا - الهولندية - CBG-MEB (College ter Beoordeling van Geneesmiddelen)

artuvetrin - test epithelia

nextmune b.v. - epithelia allergenen - oplossing voor injectie - epithelia allergenen 100 µg/ml, - allergens - honden