Lacosamide Adroiq Europeiska unionen - svenska - EMA (European Medicines Agency)

lacosamide adroiq

extrovis eu ltd. - lakosamid - epilepsi - antiepileptika, - lacosamide adroiq is indicated as monotherapy in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 2 years of age with epilepsy. lacosamide adroiq is indicated as adjunctive therapyin the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 2 years of age with epilepsy. in the treatment of primary generalised tonic-clonic seizures in adults, adolescents and children from 4 years of age with idiopathic generalised epilepsy.

Yesafili Europeiska unionen - svenska - EMA (European Medicines Agency)

yesafili

viatris limited - aflibercept - macular edema; retinal vein occlusion; diabetic retinopathy; myopia, degenerative; diabetes complications - ögonsjukdomar - yesafili is indicated for adults for the treatment ofneovascular (wet) age-related macular degeneration (amd) (see section 5. 1),visual impairment due to macular oedema secondary to retinal vein occlusion (branch rvo or central rvo) (see section 5. 1),visual impairment due to diabetic macular oedema (dme) (see section 5. 1),visual impairment due to myopic choroidal neovascularisation (myopic cnv) (see section 5.

Orserdu Europeiska unionen - svenska - EMA (European Medicines Agency)

orserdu

stemline therapeutics b.v. - elacestrant - bröst-neoplasmer - endokrin terapi - orserdu monotherapy is indicated for the treatment of postmenopausal women, and men, with estrogen receptor (er) positive, her2-negative, locally advanced or metastatic breast cancer with an activating esr1 mutation who have disease progression following at least one line of endocrine therapy including a cdk 4/6 inhibitor.

Erleada Europeiska unionen - svenska - EMA (European Medicines Agency)

erleada

janssen-cilag international nv - apalutamide - prostatiska neoplasmer - endokrin terapi - erleada anges:i vuxna män för behandling av icke metastaserad kastrering resistent prostatacancer (nmcrpc) som är en hög risk att utveckla metastatisk sjukdom. i vuxna män för behandling av metastaserande hormon-känsliga prostatacancer (mhspc) i kombination med androgen fattigdom terapi (adt).

Nubeqa Europeiska unionen - svenska - EMA (European Medicines Agency)

nubeqa

bayer ag - darolutamide - prostata tumörer, kastrering-resistent - endokrin terapi - nubeqa is indicated for the treatment of adult men with- non metastatic castration resistant prostate cancer (nmcrpc) who are at high risk of developing metastatic disease (see section 5. - metastatic hormone sensitive prostate cancer (mhspc) in combination with docetaxel and androgen deprivation therapy (see section 5.

Camcevi Europeiska unionen - svenska - EMA (European Medicines Agency)

camcevi

accord healthcare s.l.u. - leuprorelin mesilate - prostatiska neoplasmer - endokrin terapi - camcevi is indicated for the treatment of hormone dependent advanced prostate cancer and for the treatment of high-risk localised and locally advanced hormone dependent prostate cancer in combination with radiotherapy.

Fareston Europeiska unionen - svenska - EMA (European Medicines Agency)

fareston

orion corporation - toremifen - bröst-neoplasmer - endokrin terapi - första radhormonbehandling av hormonberoende metastatisk bröstcancer hos postmenopausala patienter. fareston rekommenderas inte för patienter med östrogen receptor-negativ tumörer.

Faslodex Europeiska unionen - svenska - EMA (European Medicines Agency)

faslodex

astrazeneca ab - fulvestrant - bröst-neoplasmer - endokrin terapi, anti-östrogener - faslodex is indicated , as monotherapy for the treatment of estrogen receptor positive, locally advanced or metastatic breast cancer in postmenopausal women:, , not previously treated with endocrine therapy, or, with disease relapse on or after adjuvant antiestrogen therapy, or disease progression on antiestrogen therapy. , , , in combination with palbociclib for the treatment of hormone receptor (hr)-positive, human epidermal growth factor receptor 2 (her2)-negative locally advanced or metastatic breast cancer in women who have received prior endocrine therapy. i pre - eller perimenopausala kvinnor, kombinationsbehandling med palbociclib bör kombineras med en luteinizing hormone releasing hormone (gnrh) agonist.

Zytiga Europeiska unionen - svenska - EMA (European Medicines Agency)

zytiga

janssen-cilag international n.v. - abirateronacetat - prostatiska neoplasmer - endokrin terapi - zytiga är markerad med prednison eller prednisolon för:behandling av metastaserande kastrering resistent prostatacancer hos vuxna män som är asymptomatiska eller lindrigt symptomatiska efter bortfall av androgen fattigdom terapi i vilken kemoterapi är ännu inte kliniskt indicatedthe behandling av metastaserande kastrering resistent prostatacancer hos vuxna män vars sjukdom har kommit på eller efter ett docetaxel-baserad kemoterapi regim.

Abiraterone Accord Europeiska unionen - svenska - EMA (European Medicines Agency)

abiraterone accord

accord healthcare s.l.u. - abirateronacetat - prostatiska neoplasmer - endokrin terapi - 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.