Zarzio Unione Europea - inglese - EMA (European Medicines Agency)

zarzio

sandoz gmbh - filgrastim - neutropenia; hematopoietic stem cell transplantation; cancer - immunostimulants, - reduction in the duration of neutropenia and the incidence of febrile neutropenia in patients treated with established cytotoxic chemotherapy for malignancy (with the exception of chronic myeloid leukaemia and myelodysplastic syndromes) and reduction in the duration of neutropenia in patients undergoing myeloablative therapy followed by bone-marrow transplantation considered to be at increased risk of prolonged severe neutropenia. the safety and efficacy of filgrastim are similar in adults and children receiving cytotoxic chemotherapy.mobilisation of peripheral blood progenitor cells (pbpc).in children and adults with severe congenital, cyclic, or idiopathic neutropenia with an absolute neutrophil count (anc) of ≤0.5 x 109/l, and a history of severe or recurrent infections, long term administration of filgrastim is indicated to increase neutrophil counts and to reduce the incidence and duration of infection-related events.treatment of persistent neutropenia (anc ≤ 1.0 x 109/l) in patients with advanced hiv infection, in order to reduce the risk of bacterial infections when other therapeutic options are inappropriate.

Ratiograstim Unione Europea - inglese - EMA (European Medicines Agency)

ratiograstim

ratiopharm gmbh - filgrastim - neutropenia; hematopoietic stem cell transplantation; cancer - immunostimulants, - ratiograstim is indicated for the reduction in the duration of neutropenia and the incidence of febrile neutropenia in patients treated with established cytotoxic chemotherapy for malignancy (with the exception of chronic myeloid leukaemia and myelodysplastic syndromes) and for the reduction in the duration of neutropenia in patients undergoing myeloablative therapy followed by bone-marrow transplantation considered to be at increased risk of prolonged severe neutropenia. the safety and efficacy of filgrastim are similar in adults and children receiving cytotoxic chemotherapy.ratiograstim is indicated for the mobilisation of peripheral blood progenitor cells (pbpc).in patients, children or adults, with severe congenital, cyclic, or idiopathic neutropenia with an absolute neutrophil count (anc) of ≤ 0.5 x 109/l, and a history of severe or recurrent infections, long term administration of ratiograstim is indicated to increase neutrophil counts and to reduce the incidence and duration of infection-related events.ratiograstim is indicated for the treatment of persistent neutropenia (anc ≤ 1.0 x 109/l) in patients with advanced hiv infection, in order to reduce the risk of bacterial infections when other options to manage neutropenia are inappropriate.

Tevagrastim Unione Europea - inglese - EMA (European Medicines Agency)

tevagrastim

teva gmbh - filgrastim - neutropenia; hematopoietic stem cell transplantation; cancer - immunostimulants, - tevagrastim is indicated for the reduction in the duration of neutropenia and the incidence of febrile neutropenia in patients treated with established cytotoxic chemotherapy for malignancy (with the exception of chronic myeloid leukaemia and myelodysplastic syndromes) and for the reduction in the duration of neutropenia in patients undergoing myeloablative therapy followed by bone-marrow transplantation considered to be at increased risk of prolonged severe neutropenia. the safety and efficacy of filgrastim are similar in adults and children receiving cytotoxic chemotherapy.tevagrastim is indicated for the mobilisation of peripheral blood progenitor cells (pbpc).in patients, children or adults, with severe congenital, cyclic, or idiopathic neutropenia with an absolute neutrophil count (anc) of 0.5 x 109/l, and a history of severe or recurrent infections, long term administration of tevagrastim is indicated to increase neutrophil counts and to reduce the incidence and duration of infection-related events.tevagrastim is indicated for the treatment of persistent neutropenia (anc less than or equal to 1.0 x 109/l) in patients with advanced hiv infection, in order to reduce the risk of bacterial infections when other options to manage neutropenia are inappropriate.

NEUPOGEN SOLUTION Canada - inglese - Health Canada

neupogen solution

amgen canada inc - filgrastim - solution - 300mcg - filgrastim 300mcg - hematopoietic agents

STEMGEN KIT Canada - inglese - Health Canada

stemgen kit

biovitrum ab (publ) - ancestim; water - kit - 1875mcg; 5ml - ancestim 1875mcg; water 5ml - hematopoietic agents

STEMGEN KIT Canada - inglese - Health Canada

stemgen kit

biovitrum ab (publ) - ancestim; water - kit - 2500mcg; 5ml - ancestim 2500mcg; water 5ml - hematopoietic agents

NEULASTA SOLUTION Canada - inglese - Health Canada

neulasta solution

amgen canada inc - pegfilgrastim - solution - 10mg - pegfilgrastim 10mg - hematopoietic agents

NEUPOGEN SOLUTION Canada - inglese - Health Canada

neupogen solution

amgen canada inc - filgrastim - solution - 600mcg - filgrastim 600mcg - hematopoietic agents

NEUPOGEN SOLUTION Canada - inglese - Health Canada

neupogen solution

amgen canada inc - filgrastim - solution - 600mcg - filgrastim 600mcg - hematopoietic agents

GRASTOFIL SOLUTION Canada - inglese - Health Canada

grastofil solution

apotex inc - filgrastim - solution - 300mcg - filgrastim 300mcg - hematopoietic agents