Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

Øresund pharma aps - natriumnitroprussiddihydrat - pulver til infusionsvæske, opløsning - 60 mg

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

laboratoire francais du fractionnement et des biotechnologies - eptacog beta (activated) - hemophilia a; hemophilia b - antihemorrhagics - cevenfacta is indicated in adults and adolescents (12 years of age and older) for the treatment of bleeding episodes and for the prevention of bleeding in those undergoing surgery or invasive procedures in the following patient groups:in patients with congenital haemophilia with high-responding inhibitors to coagulation factors viii or ix (i. ≥5 bethesda units (bu)); in patients with congenital haemophilia with low titre inhibitors (bu.

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

virbac s.a. - osateronacetat - urologicals - hunde - behandling af godartet prostatisk hypertrofi (bph) hos hanhunde.

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

dendreon uk ltd - autologe perifere blodmononukleære celler indbefattende mindst 50 millioner autologe cd54 + -celler aktiveret med prostatasyre phosphatase granulocyt-makrofag kolonistimulerende faktor - prostatiske neoplasmer - andre immunstimulerende midler - provenge er indiceret til behandling af asymptomatiske eller minimalt symptomatisk metastatisk (ikke-visceral) kastreret-resistente prostatakræft i mandlige voksne i hvem kemoterapi ikke er endnu klinisk indiceret.

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

bayer ag - radium (223ra) dichloride - prostatiske neoplasmer - terapeutiske radioaktive lægemidler - xofigo er indiceret til behandling af voksne med kastreringsresistent prostatacancer, symptomatiske knoglemetastaser og ingen kendte viscerale metastaser.

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

ferring pharmaceuticals a/s - degarelix - prostatiske neoplasmer - endokrine terapi - firmagon is a gonadotrophin releasing hormone (gnrh) antagonist indicated:- for treatment of adult male patients with advanced hormone-dependent prostate cancer. - for treatment of high-risk localised and locally advanced hormone dependent prostate cancer in combination with radiotherapy. - as neo-adjuvant treatment prior to radiotherapy in patients with high-risk localised or locally advanced hormone dependent prostate cancer.

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

dechra regulatory b.v. - desoxycortonpivalat - kortikosteroider til systemisk brug - hunde - til brug som erstatning terapi for mineralocorticoid mangel på hunde med primær hypoadrenocorticism (addison ' s sygdom).

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

baxalta innovations gmbh - nonacog gamma - hæmofili b - antihemorrhagics - behandling og profylakse af blødning hos patienter med hæmofili b (medfødt faktor ix-mangel).

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

biomarin international limited - valoctocogene roxaparvovec - antihemorrhagics - treatment of severe haemophilia a (congenital factor viii deficiency) in adult patients without a history of factor viii inhibitors and without detectable antibodies to adeno-associated virus serotype 5 (aav5).

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

lipomed gmbh - thalidomid - multipelt myelom - immunosuppressiva - thalidomide lipomed in combination with melphalan and prednisone is indicated as first line treatment of patients with untreated multiple myeloma, aged ≥ 65 years or ineligible for high dose chemotherapy. thalidomide lipomed is prescribed and dispensed in accordance with the thalidomide lipomed pregnancy prevention programme (see section 4.