MELPHALAN ZENTIVA 50MG Prášek a rozpouštědlo pro injekční/infuzní roztok Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

melphalan zentiva 50mg prášek a rozpouštědlo pro injekční/infuzní roztok

zentiva, k.s., praha array - 21067 melfalan-hydrochlorid - prášek a rozpouštědlo pro injekční/infuzní roztok - 50mg - melfalan

Phelinun Evropská unie - čeština - EMA (European Medicines Agency)

phelinun

adienne s.r.l. s.u. - melphalan hydrochloride - multiple myeloma; hodgkin disease; lymphoma, non-hodgkin; precursor cell lymphoblastic leukemia-lymphoma; leukemia, myeloid, acute; neuroblastoma; ovarian neoplasms; hematopoietic stem cell transplantation - antineoplastická činidla - high-dose of phelinun used alone or in combination with other cytotoxic medicinal products and/or total body irradiation is indicated in the treatment of:multiple myeloma,malignant lymphoma (hodgkin, non-hodgkin lymphoma),acute lymphoblastic and myeloblastic leukemia,childhood neuroblastoma,ovarian cancer,mammary adenocarcinoma. phelinun in combination with other cytotoxic medicinal products is indicated as reduced intensity conditioning (ric) treatment prior to allogeneic haematopoietic stem cell transplantation (allo-hsct) in malignant haematological diseases in adults. phelinun in combination with other cytotoxic medicinal products is indicated as conditioning regimen prior to allogeneic haematopoietic stem cell transplantation in haematological diseases in the paediatric population as:myeloablative conditioning (mac) treatment in case of malignant haematological diseasesric treatment in case of non-malignant haematological diseases.

CANEPHRON Obalená tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

canephron obalená tableta

bionorica se, neumarkt array - 2936 libeČkovÝ koŘen; 3021 rozmarÝnovÝ list; 2276 zemĚŽluČovÁ naŤ - obalená tableta - fytofarmaka a ŽivoČiŠnÉ produkty (ČeskÁ atc skupina)

CANEPHRON FORTE Obalená tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

canephron forte obalená tableta

bionorica se, neumarkt array - 2276 zemĚŽluČovÁ naŤ; 2936 libeČkovÝ koŘen; 3021 rozmarÝnovÝ list - obalená tableta - jinÁ urologika

MILOXAN Injekční suspenze Česká republika - čeština - USKVBL (Ústav Pro Státní Kontrolu Veterinárních Biopreparátů A Léčiv)

miloxan injekční suspenze

boehringer ingelheim animal health france scs - clostridium - injekční suspenze - inaktivované bakteriální vakcíny (včetně mycoplasma, toxoid a chlamydie vakcín) - kozy, prasata, ovce, skot

Pepaxti Evropská unie - čeština - EMA (European Medicines Agency)

pepaxti

oncopeptides ab - melphalan flufenamide hydrochloride - mnohočetný myelom - antineoplastická činidla - pepaxti is indicated, in combination with dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least three prior lines of therapies, whose disease is refractory to at least one proteasome inhibitor, one immunomodulatory agent, and one anti-cd38 monoclonal antibody, and who have demonstrated disease progression on or after the last therapy. for patients with a prior autologous stem cell transplantation, the time to progression should be at least 3 years from transplantation (see section 4.

Xevudy Evropská unie - čeština - EMA (European Medicines Agency)

xevudy

glaxosmithkline trading services limited - sotrovimab - covid-19 virus infection - imunitní séra a imunoglobuliny, - xevudy is indicated for the treatment of adults and adolescents (aged 12 years and over and weighing at least 40 kg) with coronavirus disease 2019 (covid-19) who do not require oxygen supplementation and who are at increased risk of progressing to severe covid-19.

Flebogamma DIF (previously Flebogammadif) Evropská unie - čeština - EMA (European Medicines Agency)

flebogamma dif (previously flebogammadif)

instituto grifols s.a. - normální lidský imunoglobulin - mucocutaneous lymph node syndrome; guillain-barre syndrome; bone marrow transplantation; purpura, thrombocytopenic, idiopathic; immunologic deficiency syndromes - imunitní séra a imunoglobuliny, - 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.

ALKERAN 2MG Potahovaná tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

alkeran 2mg potahovaná tableta

aspen pharma trading limited, dublin array - 1571 melfalan - potahovaná tableta - 2mg - melfalan

ALKERAN 50MG Prášek a rozpouštědlo pro injekční/infuzní roztok Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

alkeran 50mg prášek a rozpouštědlo pro injekční/infuzní roztok

aspen pharma trading limited, dublin array - 1571 melfalan - prášek a rozpouštědlo pro injekční/infuzní roztok - 50mg - melfalan