HCPCS Q5127: Pegfilgrastim-fpgk (Stimufend) 0.5 mg Injection
HCPCS Level II code Q5127 designates the 0.5 mg injection of pegfilgrastim-fpgk (brand name Stimufend), a biosimilar granulocyte colony-stimulating factor used to reduce the incidence of infection in patients receiving myelosuppressive chemotherapy. This code matters nationally as biosimilar biologics expand therapeutic options and affect coverage, utilization, and cost management across payers.
Key payers reviewed include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of clinical context for pegfilgrastim biosimilars, typical sites of service where Q5127 is billed, and payer coverage landscapes. The publication summarizes benchmarks for utilization and financial impacts where available, recent policy considerations around biosimilar substitution and billing, and coding clarifications relevant to administration of pegfilgrastim biosimilars.
The report is intended for revenue cycle managers, oncology clinicians, and policy analysts seeking a national-level reference on coding, clinical context, and payer patterns for biosimilar pegfilgrastim represented by HCPCS Level II code Q5127.
Customize your policy alerts
Sign up for hcpcs Q5127 policy alerts
Get alerted when payer policies referencing Q5127 are released or updated.
Monitor payer policy activity
Billing Code Overview
HCPCS Level II code Q5127 represents the injection formulation pegfilgrastim-fpgk (Stimufend), a biosimilar product dosed at 0.5 mg. This code is used to report administration of the specified biosimilar pegfilgrastim preparation for indications consistent with granulocyte colony-stimulating factor therapy.
Service type: Injection administration of a biosimilar biologic
Typical site of service: Outpatient infusion clinic, oncology clinic, or physician office
Data not available in the input.