Pedea Den Europæiske Union - dansk - EMA (European Medicines Agency)

pedea

recordati rare diseases - ibuprofen - ductus arteriosus, patent - hjertetapi - behandling af et hæmodynamisk signifikant patent ductus arteriosus hos nyfødte nyfødte børn under 34 uger af graviditetsalderen.

Filsuvez Den Europæiske Union - dansk - EMA (European Medicines Agency)

filsuvez

amryt pharmaceuticals dac - dry extract from birch bark (der 5-10 : 1), extraction solvent n-heptane 95% (w/w) - epidermolysis bullosa dystrophica; epidermolysis bullosa, junctional - præparater til behandling af sår og sår - treatment of partial thickness wounds associated with dystrophic and junctional epidermolysis bullosa (eb) in patients 6 months and older.

Lojuxta Den Europæiske Union - dansk - EMA (European Medicines Agency)

lojuxta

amryt pharmaceuticals dac - lomitapide - hyperkolesterolæmi - lipid modificerende midler - lojuxta er indiceret som et supplement til en low‑fat kost og andre lipid‑lowering lægemidler med eller uden lav density lipoprotein (ldl) aferese hos voksne patienter med homozygot familiær hyperkolesterolæmi (hofh). genetiske bekræftelse af hofh skal indhentes, når det er muligt. andre former for primær hyperlipoproteinaemia og sekundære årsager til hypercholesterolaemia e. nefrotisk syndrom, hypothyroidisme) skal udelukkes,.

Myalepta Den Europæiske Union - dansk - EMA (European Medicines Agency)

myalepta

amryt pharmaceuticals dac - metreleptin - lipodystrofi, familiær delvis - andre alimentary tract and metabolism produkter, - myalepta er indiceret som et supplement til kost som en substitutionsterapi til at behandle de komplikationer af leptin mangel i lipodystrofi (ld) patienter med bekræftet medfødte generelle ld (berardinelli-seip syndrom) eller erhvervet generelle ld (lawrence syndrom) hos voksne og børn på 2 år og abovewith bekræftet familiær delvis ld eller erhvervet, delvis ld (barraquer-simons syndrom), hos voksne og børn på 12 år og derover, for hvem standard-behandlinger har undladt at opnå tilstrækkelig metabolisk kontrol.

Sibnayal Den Europæiske Union - dansk - EMA (European Medicines Agency)

sibnayal

advicenne s.a. - potassium citrate monohydrated, potassium hydrogen carbonate - acidosis, renal tubular - mineral supplements - sibnayal is indicated for the treatment of distal renal tubular acidosis (drta) in adults, adolescents and children aged one year and older.

Olysio Den Europæiske Union - dansk - EMA (European Medicines Agency)

olysio

janssen-cilag international nv - simeprevir - hepatitis c kronisk - antivirale midler til systemisk anvendelse - olysio er indiceret i kombination med andre lægemidler til behandling af kronisk hepatitis c (chc) hos voksne patienter. for at hepatitis c virus (hcv) genotype specifikke aktivitet.

Zytiga Den Europæiske Union - dansk - EMA (European Medicines Agency)

zytiga

janssen-cilag international n.v. - abiraterone acetat - prostatiske neoplasmer - endokrine terapi - zytiga er angivet med prednison eller prednisolon for:behandling af metastatisk kastration resistent prostatakræft hos voksne mænd, der er asymptomatiske eller mildt symptomatisk efter svigt af androgen deprivation terapi i hvem kemoterapi er endnu ikke klinisk indicatedthe behandling af metastatisk kastration resistent prostatakræft hos voksne mænd, hvis sygdommen har udviklet sig på eller efter en docetaxel-baseret kemoterapi.

Abiraterone Accord Den Europæiske Union - dansk - 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 Den Europæiske Union - dansk - 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 Den Europæiske Union - dansk - 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.