WebOct 15, 2024 · Fulphila has been approved by the Food and Drug Administration (FDA) for the treatment and prevention of (febrile) neutropenia caused by chemotherapy or … Web2. Fulphila administered while patient is receiving myelosuppressive chemotherapy medications [J9000 series], AND 3. Fulphila is administered every 14 days or more, AND 4. Fulphila is not being used concurrently with long-acting or short-acting granulocyte colony stimulating factors (e.g. filgrastim or pegfilgrastim drugs), AND 5.
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