Carmustine medac (previously Carmustine Obvius) Unia Europejska - polski - EMA (European Medicines Agency)

carmustine medac (previously carmustine obvius)

medac gesellschaft für klinische spezialpräparate mbh - karmustinom - hodgkin disease; lymphoma, non-hodgkin - Środki przeciwnowotworowe - carmustine is indicated n adults in the following malignant neoplasms as a single agent or in combination with other antineoplastic agents and/or other therapeutic measures (radiotherapy, surgery): , brain tumours (glioblastoma, brain-stem gliomas, medulloblastoma, astrocytoma and ependymoma), brain metastases, secondary therapy in non-hodgkin’s lymphoma and hodgkin’s disease, as conditioning treatment prior to autologous haematopoietic progenitor cell transplantation (hpct) in malignant haematological diseases (hodgkin’s disease / non-hodgkin’s lymphoma).

Ferrologic 20 mg/ml 20 mg Fe 3+/ml roztwór do wstrzykiwań, koncentrat do sporządzania roztworu do infuzji Polska - polski - URPL (Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych)

ferrologic 20 mg/ml 20 mg fe 3+/ml roztwór do wstrzykiwań, koncentrat do sporządzania roztworu do infuzji

fresenius medical care nephrologica deutschland gmbh - ferri hydroxidum saccharum - roztwór do wstrzykiwań, koncentrat do sporządzania roztworu do infuzji - 20 mg fe 3+/ml

Pepaxti Unia Europejska - polski - EMA (European Medicines Agency)

pepaxti

oncopeptides ab - melphalan flufenamide hydrochloride - szpiczak mnogi - Środki przeciwnowotworowe - 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.

Bendamustine Eugia 2,5 mg/ml Proszek do sporządzania koncentratu roztworu do infuzji Polska - polski - URPL (Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych)

bendamustine eugia 2,5 mg/ml proszek do sporządzania koncentratu roztworu do infuzji

eugia pharma (malta) ltd. - bendamustini hydrochloridum monohydricum - proszek do sporządzania koncentratu roztworu do infuzji - 2,5 mg/ml

Plerixafor Accord Unia Europejska - polski - EMA (European Medicines Agency)

plerixafor accord

accord healthcare s.l.u. - plerixafor - multiple myeloma; hematopoietic stem cell transplantation - Иммуностимуляторы, - 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.