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filgrastim (Ratiograstim®)

 

Following a full submission

AWMSG advice

Status: Recommended

Filgrastim (Ratiograstim®) is recommended as an option for use within NHS Wales in the treatment of neutropenia:

  • 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.
  • For the mobilisation of peripheral blood progenitor cells (PBPC).
  • To increase neutrophil counts and to reduce the incidence and duration of infection-related events in patients 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.
  • For the treatment of persistent neutropenia (ANC less than or equal to 1.0 x 10⁹/L) in patients with advanced human immunodeficiency virus (HIV) infection, in order to reduce the risk of bacterial infections when other options to manage neutropenia are inappropriate.

AWMSG is of the opinion that filgrastim (Ratiograstim®) is not suitable for shared care within NHS Wales. Biosimilars should be prescribed by brand name to avoid automatic substitution and ensure consistency in provision.

 Final Recommendation: filgrastim (ratiograstim) 366 (PDF, 274Kb)

Medicine details

Medicine name filgrastim (Ratiograstim®)
Formulation solution for injection/infusion
Reference number 366
Indication
  • 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.
  • 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 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 options to manage neutropenia are inappropriate
Company Ratiopharm UK Ltd
BNF chapter Nutrition & blood
Submission type Full
Status Recommended
Advice number 1609
NMG meeting date 15/07/2009
AWMSG meeting date 12/08/2009
Ratification by Welsh Government 11/09/2009
Date of issue 11/09/2009
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