Fervin Pulver Dinamarca - danès - SEGES Landbrug & Fødevarer

fervin pulver

schering - alloxydim-na, alloxydim - pulver - 750 g/kg alloxydim-na ; (~ 668 g/kg alloxydim

Arti-Cell Forte Unió Europea - danès - EMA (European Medicines Agency)

arti-cell forte

boehringer ingelheim vetmedica gmbh - chondrogenic induceret enhovede allogen perifert blod-afledte mesenchymal stem cells - andre midler mod forstyrrelser i muskel-skeletsystemet - heste - reduktion af mild til moderat periodisk halthed, der er forbundet med ikke-septisk ledbetændelse i heste.

Thiotepa Riemser Unió Europea - danès - EMA (European Medicines Agency)

thiotepa riemser

esteve pharmaceuticals gmbh - thiotepa - hematopoietic stem cell transplantation; neoplasms - antineoplastiske midler - thiotepa riemser is indicated, in combination with other chemotherapy medicinal products:with or without total body irradiation (tbi), as conditioning treatment prior to allogeneic or autologous haematopoietic progenitor cell transplantation (hpct) in haematological diseases in adult and paediatric patients;when high dose chemotherapy with hpct support is appropriate for the treatment of solid tumours in adult and paediatric patients. thiotepa riemser is indicated, in combination with other chemotherapy medicinal products:with or without total body irradiation (tbi), as conditioning treatment prior to allogeneic or autologous haematopoietic progenitor cell transplantation (hpct) in haematological diseases in adult and paediatric patients;when high dose chemotherapy with hpct support is appropriate for the treatment of solid tumours in adult and paediatric patients.

Busulfan Fresenius Kabi Unió Europea - danès - EMA (European Medicines Agency)

busulfan fresenius kabi

fresenius kabi deutschland gmbh - busulfan - hematopoietisk stamcelletransplantation - alkylsulfonater - busulfan fresenius kabi efterfulgt af cyclophosphamid (bucy2) er indiceret som konditionerende behandling før konventionelle hæmatopoietiske stamceller celle transplantation (hpct) hos voksne patienter, når kombinationen er betragtes som den bedste tilgængelige mulighed. busulfan fresenius kabi efterfulgt af cyclophosphamid (bucy4) eller melphalan (bumel) er angivet som condition behandling forud for konventionelle hæmatopoietisk stamcelletransplantation i pædiatriske patienter.

CA 2239 Suspensionskoncentrat Dinamarca - danès - SEGES Landbrug & Fødevarer

ca 2239 suspensionskoncentrat

nufarm deutschland gmbh - bromoxynil - suspensionskoncentrat - 401,6 g/l bromoxynil

Lentacol Universal Flydende middel Dinamarca - danès - SEGES Landbrug & Fødevarer

lentacol universal flydende middel

nufarm deutschland gmbh - thiram - flydende middel - 135 g/l thiram

Flebogamma DIF (previously Flebogammadif) Unió Europea - danès - EMA (European Medicines Agency)

flebogamma dif (previously flebogammadif)

instituto grifols s.a. - humant normalt immunglobulin - mucocutaneous lymph node syndrome; guillain-barre syndrome; bone marrow transplantation; purpura, thrombocytopenic, idiopathic; immunologic deficiency syndromes - immune sera og immunoglobuliner, - replacement therapy in adults, children and adolescents (0-18 years) in: , primary immunodeficiency syndromes with impaired antibody production;, hypogammaglobulinaemia and recurrent bacterial infections in patients with chronic lymphocytic luekaemia, in whom prophylactic antibiotics have failed;, hypogammaglobulinaemia and recurrent bacterial infections in plateau-phase-multiple-myeloma patients who failed to respond to pneumococcal immunisation;, hypogammaglobulinaemia in patients after allogenic haematopoietic-stem-cell transplantation (hsct);, congenital aids with recurrent bacterial infections. , immunomodulation in adults, children and adolescents (0-18 years) in: , primary immune thrombocytopenia (itp), in patients at high risk of bleeding or prior to surgery to correct the platelet count;, guillain barré syndrome;, kawasaki disease.

Blincyto Unió Europea - danès - EMA (European Medicines Agency)

blincyto

amgen europe b.v. - blinatumomab - forløbercellelimfoblastisk leukæmi-lymfom - antineoplastiske midler - blincyto is indicated as monotherapy for the treatment of adults with cd19 positive relapsed or refractory b precursor acute lymphoblastic leukaemia (all). patients with philadelphia chromosome positive b-precursor all should have failed treatment with at least 2 tyrosine kinase inhibitors (tkis) and have no alternative treatment options. blincyto is indicated as monotherapy for the treatment of adults with philadelphia chromosome negative cd19 positive b-precursor all in first or second complete remission with minimal residual disease (mrd) greater than or equal to 0. blincyto is indicated as monotherapy for the treatment of paediatric patients aged 1 year or older with philadelphia chromosome negative cd19 positive b precursor all which is refractory or in relapse after receiving at least two prior therapies or in relapse after receiving prior allogeneic haematopoietic stem cell transplantation. blincyto is indicated as monotherapy for the treatment of paediatric patients aged 1 year or older with high-risk first relapsed philadelphia chromosome negative cd19 positive b-precursor all as part of the consolidation therapy (see section 4.

Nutri-Phite Magnum S Flydende middel Dinamarca - danès - SEGES Landbrug & Fødevarer

nutri-phite magnum s flydende middel

manglende oplysninger - uspecificeret - flydende middel - 0 g/l uspecificeret

Activus Super Suspensionskoncentrat Dinamarca - danès - SEGES Landbrug & Fødevarer

activus super suspensionskoncentrat

adama northern europe b.v. - pendimethalin, diflufenican - suspensionskoncentrat - 400 g/l pendimethalin ; 40 g/l diflufenican