Rolvedon

September 9, 2022

Rolvedon™ (eflapegrastim-xnst) injection has been approved to decrease the incidence of chemotherapy-induced febrile neutropenia in adult patients.

  • Manufactured by Spectrum Pharmaceuticals, Inc., Rolvedon™ injection is a long-acting granulocyte colony-stimulating factor (G-CSF) with a novel Spectrum has received an indication to decrease the incidence of infection, as manifested by febrile neutropenia, in adult patients with non-myeloid malignancies receiving myelosuppressive anti-cancer drugs associated with clinically significant incidence of febrile neutropenia.
  • Rolvedon is contraindicated in patients with a history of serious allergic reactions to eflapegrastim, pegfilgrastim or filgrastim Reactions may include anaphylaxis.
  • It is expected to be available in fourth quarter 2022.

Related News

demo-attachment-261-Group-56
demo-attachment-606-Group-43
demo-attachment-1121-Rectangle-602

Benefit Advisors & Employees - Want to know more?

Members: Please call the number on the back of your ID card or e-mail member.services@benecardpbf.com Clients: Contact your Client Relations Manager
demo-attachment-180-Group-4