Ilomedin 20 mikrog/ ml Նորվեգիա - Նորվեգերեն - Statens legemiddelverk

ilomedin 20 mikrog/ ml

bayer ab - solna - iloprosttrometamol - konsentrat til infusjonsvæske, oppløsning - 20 mikrog/ ml

Arti-Cell Forte Եվրոպական Միություն - Նորվեգերեն - EMA (European Medicines Agency)

arti-cell forte

boehringer ingelheim vetmedica gmbh - chondrogenic indusert equine allogen perifert blod-avledet mesenchymal stem cells - andre legemidler for forstyrrelser i muskel-skjelettsystemet - hester - reduksjon av mild til moderat tilbakevendende halting forbundet med ikke-septisk leddbetennelse i hester.

Coxor 300 mg Նորվեգիա - Նորվեգերեն - Statens legemiddelverk

coxor 300 mg

asamedic as (1) - acetylsalisylsyre - pulver og væske til mikstur, oppløsning - 300 mg

Thiotepa Riemser Եվրոպական Միություն - Նորվեգերեն - EMA (European Medicines Agency)

thiotepa riemser

esteve pharmaceuticals gmbh - tiotepa - 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.

Theracap 131TM - Նորվեգիա - Նորվեգերեն - Statens legemiddelverk

theracap 131tm -

ge healthcare buchler gmbh & co. kg - natriumjodid (131i) - kapsel, hard

Flebogamma DIF (previously Flebogammadif) Եվրոպական Միություն - Նորվեգերեն - 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 immunglobuliner, - 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 Եվրոպական Միություն - Նորվեգերեն - EMA (European Medicines Agency)

blincyto

amgen europe b.v. - blinatumomab - forløpercellelymfoblastisk leukemi-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.

Zalmoxis Եվրոպական Միություն - Նորվեգերեն - EMA (European Medicines Agency)

zalmoxis

molmed spa - allogene t celler genmodifiserte med en retroviral vektor koding for en avkortet form for menneskelig lav affinitet nerve vekstfaktor reseptor (Δlngfr) og herpes simplex jeg virus thymidine kinase (hsv-tk mut2) - hematopoietic stem cell transplantation; graft vs host disease - antineoplastiske midler - zalmoxis er angitt som tilleggsbehandling behandling i haploidentical haematopoietic stilk cellen transplantasjon (hsct) av voksen pasienter med høy risiko hematologisk malignitet.