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Pegfilgrastim-jmdb (Fulphila)

A self-injected biosimilar of pegfilgrastim (a Neulasta biosimilar, Fulphila) — a long-acting white-blood-cell growth factor given once per chemotherapy cycle to lower the chance of infection from a low neutrophil count (febrile neutropenia).

Plan year 2027 · Source: CMS · Checked 2026-10-31

How Medicare covers it

Part D (self-injected syringes used at home where a plan lists them). Part B covers the clinician-given injection where the CMS Part B spending file carries it (HCPCS Q5108 — see the Part B basis in this package). Part A during a covered inpatient stay.

Coverage details
Part B statusCMS Part B Spending by Drug HCPCS file (RY26, data through 2024) carries Q5108 (injection, pegfilgrastim-jmdb (fulphila), biosimilar, 0.5 mg): the clinician-given biosimilar path has a Part B basis; the self-injected home form is the Part D aggregation in this package.
Medicare AdvantageMost Medicare Advantage plans that include drug coverage (MAPD plans) use the same formulary-and-tier system; the plan's own drug list decides coverage and copay — check the plan's formulary.
Medicare Supplement (Medigap)Medicare Supplement (Medigap) plans sold today do not include prescription drug coverage; drug coverage comes from Part D or an MAPD plan.

What it treats

Fulphila (pegfilgrastim-jmdb), a biosimilar to Neulasta (pegfilgrastim), is used to decrease the incidence of infection, as shown by febrile neutropenia (fever with a low neutrophil count), in patients with non-myeloid cancers who are receiving myelosuppressive anti-cancer drugs that are associated with a clinically significant incidence of febrile neutropenia. It is not indicated for mobilizing peripheral blood progenitor cells for stem cell transplantation, and it is not indicated for increasing survival after radiation exposure.

What it is for, in depth

Fulphila is a biosimilar of Neulasta (pegfilgrastim), which means it is highly similar to Neulasta with no clinically meaningful differences. It is prescribed for people with cancers that are not myeloid cancers who are getting chemotherapy that strongly lowers the white blood cell count, putting them at risk of febrile neutropenia — fever when infection-fighting neutrophils are at their lowest, which can be life-threatening. It is a supportive care drug, not a cancer treatment: one shot per chemotherapy cycle shortens the low-count period and lowers the chance of infection. Unlike some other pegfilgrastim products, Fulphila's label covers only the chemotherapy use, not the radiation exposure use. It comes only as a 6 mg/0.6 mL single-dose prefilled syringe for injection under the skin, with weight-based dosing in the label for children under 45 kg.

How it works

It is a leukocyte growth factor, also called a colony-stimulating factor. It binds to receptors on blood-forming cells in the bone marrow and tells them to make more neutrophils, a type of white blood cell that fights infection. That shortens the time the white blood cell count stays dangerously low after chemotherapy.

How it is taken

The dose is a single 6 mg shot under the skin (subcutaneous injection) once per chemotherapy cycle. Do not give it between 14 days before and 24 hours after cytotoxic chemotherapy. For children weighing less than 45 kg, the label gives weight-based doses (for example 1.5 mg for 10 to 20 kg, 2.5 mg for 21 to 30 kg, and 4 mg for 31 to 44 kg), but the prefilled syringe is not designed for direct administration of doses under 6 mg. Fulphila comes only as a 6 mg/0.6 mL single-dose prefilled syringe for manual use. Let the syringe reach room temperature for at least 30 minutes before use, and discard it if left at room temperature for more than 72 hours.

Common side effects

The most common side effects (at least 5% more often than with placebo in trials) are bone pain and pain in an arm or leg.

Serious warnings

Serious risks include splenic rupture, which can be fatal — report pain in the left upper belly or left shoulder tip; acute respiratory distress syndrome (ARDS), a serious lung problem; serious allergic reactions including anaphylaxis; severe and sometimes fatal sickle cell crises in people with sickle cell disorders; glomerulonephritis, a kidney problem; very high white blood cell counts (leukocytosis); low platelet counts (thrombocytopenia); capillary leak syndrome; a possible growth-stimulating effect on tumor cells; myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML), which are monitored for in patients with breast and lung cancer who also get chemotherapy and/or radiation; and aortitis, inflammation of the aorta.

Who should be careful

Fulphila must not be used by anyone who has had a serious allergic reaction to a pegfilgrastim product or a filgrastim product. Tell your doctor if you have a sickle cell disorder, kidney problems, or breathing problems, and report left upper belly or shoulder pain, fever with breathing trouble, or signs of an allergic reaction right away. Tell your doctor if you are pregnant or breastfeeding.

Major interactions

The label has no drug interactions section and lists no major drug interactions. The main timing rule is about chemotherapy itself: this drug must not be given in the period from 14 days before until 24 hours after a dose of cytotoxic chemotherapy.

Cost and saving notes

If this drug is covered under your Medicare Part D plan and the cost is high, you can ask your plan for a tier exception to pay a lower cost share. If you have limited income, Extra Help (the Part D Low-Income Subsidy) can lower your Part D premiums and drug costs. In 2027, your total yearly out-of-pocket spending on covered Part D drugs is capped at $2,400, and you can spread those costs out in monthly payments through the Medicare Prescription Payment Plan.

Why it is in its tier

Pegfilgrastim-jmdb (Fulphila) sits on Tier 5 in 95.73% of the plans that list it (1816 of 1897 listing plans). Tier 5 is the specialty tier — instead of a flat copay, patients usually pay a percentage of the drug's cost (coinsurance), which is why specialty drugs feel expensive even with coverage. The data-visible drivers: It is a brand-only product with no generic version in the formulary data, and the CMS dashboard puts its average Part D spending at about $7,206 per beneficiary for 2024 — a high-cost drug, which matches where plans place it. Only 34.52% of Part D plans list it at all, so many readers will find their plan does not list it and covers a similar drug instead. The tier shown is the most common one; individual plans vary.

What official patient guides say

Fulphila (pegfilgrastim-jmdb) is a single injection under the skin from a prefilled syringe, not a pill, so you can keep your normal diet. A nurse may give it, or you may be taught to inject it yourself at home; your doctor will tell you exactly when to use it. Do not shake the syringe. Before injecting, look at the liquid closely — do not use it if the expiration date has passed or the liquid has particles or looks cloudy or discolored. Use each syringe only once, even if liquid is left, and put used syringes in a puncture-resistant container. If you inject at home, talk to your doctor ahead of time about what to do if you forget a dose, rather than guessing or doubling up. Bone pain and pain in the arms or legs are common. Store Fulphila in its carton in the refrigerator, away from direct sunlight, and do not freeze it; if you freeze it by accident, let it thaw in the refrigerator, but throw it away if the same syringe is frozen a second time. Fulphila may be kept at room temperature for up to 72 hours only.

Source: MedlinePlus — Pegfilgrastim Injection

Part D formulary coverage

Formulary summary
Most common tier5
Plans listing this drug1897
Total Part D plans5495
Share of plans listing it34.52
Formularies listing it136
TierPlans
Tier 180 plans
Tier 21 plans
Tier 51816 plans

Source: CMS Prescription Drug Plan Formulary, Pharmacy Network, and Pricing Information Files — Monthly file 2026-10-15 (plan year 2027), file 2027_20261008.zip (data.cms.gov dataset ed1496ea-23e7-41f1-9292-172fa842ccfb): basic drugs formulary file + plan information file, both dated 20261031 inside the zip; downloaded and aggregated 2026-10-30. Medication RxCUI sets resolved through the NLM RxNav (RxNorm) API.

What you pay

With Medicare Part D
Most common tierTier 5
Typical coinsurance26.0% of the price
Based on1795 plans that cover this drug · 2027 plan year

Without insurance, the cash benchmark is $3362.7767 per unit (FULPHILA 6 MG/0.6 ML SYRINGE) — about $100883.30 for 30 units. NADAC benchmark — the average price pharmacies pay (CMS, as of 2026-11-04). Pharmacy shelf prices vary.

A tier is not a price; what you pay depends on your plan, pharmacy, and benefit stage; Extra Help or Medicaid can lower it further.

Sources: CMS Plan Benefit Package + formulary data; CMS NADAC · Checked 2026-11-08

Part D spending averages (2024)

Brand nameGeneric nameTotal claims 2024Total spending 2024Total beneficiaries 2024Rank by beneficiaries 2024
FulphilaPEGfilgrastim-Jmdb34437.68154e+0610661787

Source: CMS Medicare Part D Spending by Drug (Drug Spending Dashboard), release RY26 P04 V10, data through 2024 (DSD_PTD_RY26_P04_V10_DY24_BGM.csv), downloaded 2026-10-30

Companies covering this drug

1,897 plans from 258 companies list this drug on a formulary for 2027. Search by company or plan name, or filter by tier. Cost sharing is the plan's published amount for this drug's tier in the initial coverage stage (1-month retail supply), where the plan publishes it; a blank means the plan does not publish it.

CompanyPlanTierCopayCoinsurance

A tier is not a price; what you pay depends on your plan, pharmacy, and benefit stage; Extra Help or Medicaid can lower it further.

Coverage and costs change. Drug lists (formularies), tiers, and copays can change during the year and differ by plan. Always check with your insurance company or plan directly to confirm what is covered and what you will pay.

Care and Living Guide is not connected with or endorsed by the U.S. government or the federal Medicare program. For official information visit Medicare.gov or call 1-800-MEDICARE.

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