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Description

Food and Drug Administration (FDA) to treat hematopoietic complications following acute radiation exposurefilgrastim (Neupogen, Amgen, FDA approved March 2015) (Food and Drug Administration, 2015a), pegfilgrastim (Neulasta, Amgen, FDA approved November 2015) (Food and Drug Administration, 2015b), sargramostim (Leukine, Partner Therapeutics, FDA approved March 2018) (Food and Drug Administration, 2018), and romiplostim (Nplate, Amgen, FDA approved January 2021)

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