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  • Reimbursement Connection®
  • Neulasta®
    (pegfilgrastim)
  • -- Private Payors

  • Overview
  • Amgen™ Oncology Assistance
  • Aranesp®
    (darbepoetin alfa)
  • Neulasta®
    (pegfilgrastim)
  • NEUPOGEN®
    (Filgrastim)
  • Nplate™
    (romiplostim)
  • EPOGEN®
    (Epoetin alfa)
  • Sensipar®
    (cinacalcet)
  • Enbrel®
    (etanercept)
  • Kepivance®
    (palifermin)
  • Kineret®
    (anakinra)
  • Vectibix®
    (panitumumab)
Coverage and Reimbursement
Medicaid
Medicare
Private Payors, HMOs, PPOs, Blue Cross®/Blue Shield®, and Pharmacy Benefit Plans
Private Payors, HMOs, PPOs, Blue Cross®/Blue Shield®, and Pharmacy Benefit Plans
Physician Office

Private insurers (including Blue Cross® and Blue Shield® plans, indemnity plans, and managed care plans) are likely to cover Neulasta® (pegfilgrastim) in the physician office when used for its approved indication. However, specific plans or patient contracts can vary considerably, even within the same insurer.

They may establish certain restrictions for injectables, including Neulasta®. These restrictions might include:

  • Obtaining prior authorization
  • Forwarding medical documentation, such as information regarding the patient's prescribed chemotherapy regimen
  • Abiding by participating provider restrictions

Hospital Outpatient and Inpatient

Private payors are likely to cover Neulasta® in hospital outpatient and inpatient settings.

Private payor reimbursement varies based on a patient's specific plan and the hospital's contract with the payor.

Pharmacy

Many private insurer policies offer prescription drug coverage.

Such policies typically cover and reimburse for Neulasta®. The setting and cost-sharing requirements are based on the patient-specific contract benefits.

  • Patient cost-sharing requirements may be influenced by the formulary status of Neulasta®
  • Cost-sharing also is affected by the manner the patient uses to access therapies (in network, mail order, etc.)
 

Neulasta® Indication and Important Product Safety Information

Neulasta® is indicated to decrease the incidence of infection, as manifested by febrile neutropenia, in patients with nonmyeloid malignancies receiving myelosuppressive anticancer drugs associated with a clinically significant incidence of febrile neutropenia.

Important Product Safety Information

Splenic rupture (including fatal cases), acute respiratory distress syndrome, and sickle cell crises have been reported. Allergic reactions, including anaphylaxis, have also been reported. The majority of these reactions occurred upon initial exposure. However, in rare cases, allergic reactions, including anaphylaxis, recurred within days after discontinuing anti-allergic treatment.
In a placebo-controlled trial, bone pain occurred at a higher incidence in Neulasta®-treated patients as compared to placebo-treated patients (31% vs 26%). The most common adverse events reported in either placebo- or active-controlled trials were consistent with the underlying cancer diagnosis and its treatment with chemotherapy, with the exception of bone pain.

© 2007 Amgen All Rights Reserved. Prescribing Information for Neulasta®

  • Related Links
  • Amgen Medical Information Connection™
  • Amgen Oncology Institute
  • AmgenOncology.com
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