Vegas Olie i vand emulsion Dänemark - Dänisch - SEGES Landbrug & Fødevarer

vegas olie i vand emulsion

certis europe bv - cyflufenamid - olie i vand emulsion - 51,3 g/l cyflufenamid

Takla Flydende middel Dänemark - Dänisch - SEGES Landbrug & Fødevarer

takla flydende middel

pro farm oü - kobber - flydende middel - 5,4 g/l kobber

Isemid Europäische Union - Dänisch - EMA (European Medicines Agency)

isemid

ceva santé animale - torasemide - high-ceiling diuretics, sulfonamider, almindelig - hunde - til behandling af kliniske symptomer, der er relateret til kongestiv hjerteinsufficiens, i hunde, herunder lungeødem.

Feiba 50 enheder/ml pulver og solvens til infusionsvæske, opløsning Dänemark - Dänisch - Lægemiddelstyrelsen (Danish Medicines Agency)

feiba 50 enheder/ml pulver og solvens til infusionsvæske, opløsning

baxalta innovations gmbh - koagulationsfaktor viii inhibitor passerende aktivitet - pulver og solvens til infusionsvæske, opløsning - 50 enheder/ml

Plerixafor Accord Europäische Union - Dänisch - EMA (European Medicines Agency)

plerixafor accord

accord healthcare s.l.u. - plerixafor - multiple myeloma; hematopoietic stem cell transplantation - immunostimulants, - adult patientsplerixafor accord is indicated in combination with granulocyte-colony stimulating factor (g-csf) to enhance mobilisation of haematopoietic stem cells to the peripheral blood for collection and subsequent autologous transplantation in adult patients with lymphoma or multiple myeloma whose cells mobilise poorly (see section 4. paediatric patients (1 to less than 18 years)plerixafor accord is indicated in combination with g-csf to enhance mobilisation of haematopoietic stem cells to the peripheral blood for collection and subsequent autologous transplantation in children with lymphoma or solid malignant tumours, either:- pre-emptively, when circulating stem cell count on the predicted day of collection after adequate mobilization with g-csf (with or without chemotherapy) is expected to be insufficient with regards to desired hematopoietic stem cells yield, or- who previously failed to collect sufficient haematopoietic stem cells (see section 4.

Provenge Europäische Union - Dänisch - EMA (European Medicines Agency)

provenge

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.

Mozobil Europäische Union - Dänisch - EMA (European Medicines Agency)

mozobil

sanofi b.v. - plerixafor - multiple myeloma; hematopoietic stem cell transplantation; lymphoma - immunostimulants, - mozobil angives i kombination med granulocyt koloni-stimulerende faktor til at forbedre mobiliseringen af hæmatopoietiske stamceller til de perifere blod for indsamling og efterfølgende autolog transplantation hos patienter med lymfom og flere myelomatose hvis celler mobilisere dårligt.

Olumiant Europäische Union - Dänisch - EMA (European Medicines Agency)

olumiant

eli lilly nederland b.v. - baricitinib - arthritis, reumatoid - immunosuppressiva - rheumatoid arthritisbaricitinib is indicated for the treatment of moderate to severe active rheumatoid arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more disease modifying anti rheumatic drugs (dmards). olumiant kan anvendes som monoterapi eller i kombination med methotrexat. atopic dermatitisolumiant is indicated for the treatment of moderate to severe atopic dermatitis in adult and paediatric patients 2 years of age and older who are candidates for systemic therapy. alopecia areatabaricitinib is indicated for the treatment of severe alopecia areata in adult patients (see section 5. juvenile idiopathic arthritisbaricitinib is indicated for the treatment of active juvenile idiopathic arthritis in patients 2 years of age and older who have had an inadequate response or intolerance to one or more prior conventional synthetic or biologic dmards:- polyarticular juvenile idiopathic arthritis (polyarticular rheumatoid factor positive [rf+] or negative [rf-], extended oligoarticular),- enthesitis related arthritis, and- juvenile psoriatic arthritis. baricitinib may be used as monotherapy or in combination with methotrexate.

Nutrineal PD4 peritonealdialysevæske Dänemark - Dänisch - Lægemiddelstyrelsen (Danish Medicines Agency)

nutrineal pd4 peritonealdialysevæske

baxter a/s - alanin, arginin, calciumchloriddihydrat, glycin, histidin, isoleucin, leucin, lysinhydrochlorid, magnesiumchloridhexahydrat, methionin, natriumchlorid, natriumlactat, phenylalanin, prolin, serin, threonin, tryptophan, tyrosin, valin - peritonealdialysevæske