Rapilysin Európai Unió - dán - EMA (European Medicines Agency)

rapilysin

actavis group ptc ehf - reteplase - myokardieinfarkt - antitrombotiske midler - rapilysin is indicated for the thrombolytic treatment of suspected myocardial infarction with persistent st elevation or recent left bundle branch block within 12 hours after the onset of acute-myocardial-infarction (ami) symptoms.

Zoledronic acid Teva Generics Európai Unió - dán - EMA (European Medicines Agency)

zoledronic acid teva generics

teva generics b.v - zoledronsyremonohydrat - osteoporosis; osteitis deformans - bisfosfonater - behandling af osteoporosisin post-menopausale womenin voksen menat øget risiko for fraktur, herunder dem med de seneste lavt-hip fracture trauma. behandling af osteoporose, der er forbundet med langtids systemisk glukokortikoid therapyin post-menopausale womenin voksen menat øget risiko for fraktur. behandling af pagets sygdom af knoglerne hos voksne.

Zoledronic acid Teva Pharma Európai Unió - dán - EMA (European Medicines Agency)

zoledronic acid teva pharma

teva b.v. - zoledronsyre - osteoporosis; osteitis deformans; osteoporosis, postmenopausal - narkotika til behandling af knoglesygdomme - treatment of osteoporosis: , in post-menopausal women;, in men; , at increased risk of fracture including those with a recent low-trauma hip fracture. treatment of osteoporosis associated with long-term systemic glucocorticoid therapy: , in post-menopausal women;, in men; , at increased risk of fracture. behandling af pagets sygdom af knoglerne hos voksne.

Mektovi Európai Unió - dán - EMA (European Medicines Agency)

mektovi

pierre fabre medicament - binimetinib - melanom - antineoplastiske midler - binimetinib i kombination med encorafenib er indiceret til behandling af voksne patienter med inoperabel eller metastatisk melanom med en braf v600 mutation.

Inbrija Európai Unió - dán - EMA (European Medicines Agency)

inbrija

acorda therapeutics ireland limited - levodopa - parkinsons sygdom - anti-parkinson-lægemidler - inbrija er angivet for den intermitterende behandling af episodisk motoriske fluktuationer (off episoder) hos voksne patienter med parkinsons sygdom (pd) behandles med levodopa/dopa-decarboxylase inhibitor.

Isturisa Európai Unió - dán - EMA (European Medicines Agency)

isturisa

recordati rare diseases - osilodrostat fosfat - cushing syndrome - kortikosteroider til systemisk brug - isturisa er indiceret til behandling af endogene cushings syndrom hos voksne.

Abiraterone Accord Európai Unió - dán - EMA (European Medicines Agency)

abiraterone accord

accord healthcare s.l.u. - abiraterone acetat - prostatiske neoplasmer - endokrine 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.

Abiraterone Mylan Európai Unió - dán - EMA (European Medicines Agency)

abiraterone mylan

mylan ireland limited - abiraterone acetat - prostatiske neoplasmer - endocrine therapy, other hormone antagonists and related agents - abiraterone mylan 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 indicated. the treatment of mcrpc in adult men whose disease has progressed on or after a docetaxel based chemotherapy regimen.

Abiraterone Krka Európai Unió - dán - EMA (European Medicines Agency)

abiraterone krka

krka, d.d., novo mesto - abiraterone acetat - prostatiske neoplasmer - endokrine terapi - abiraterone krka 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) (see section 5. 1)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 indicated (see section 5. 1)the treatment of mcrpc in adult men whose disease has progressed on or after a docetaxel-based chemotherapy regimen.

Xenpozyme Európai Unió - dán - EMA (European Medicines Agency)

xenpozyme

sanofi b.v. - olipudase alfa - acid sphingomyelinase deficiency (asmd) type a/b or type b - andre alimentary tract and metabolism produkter, - xenpozyme is indicated as an enzyme replacement therapy for the treatment of non-central nervous system (cns) manifestations of acid sphingomyelinase deficiency (asmd) in paediatric and adult patients with type a/b or type b.