label - Food and Drug Administration
LEUKINE is indicated to increase survival in adult and pediatric patients from birth to 17 years of age acutely exposed to myelosuppressive doses of radiation (Hematopoietic Syndrome of...
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LEUKINE is indicated to increase survival in adult and pediatric patients from birth to 17 years of age acutely exposed to myelosuppressive doses of radiation (Hematopoietic Syndrome of...
2026年3月27日 · LEUKINE is indicated to increase survival in adult and pediatric patients from birth to 17 years of age acutely exposed to myelosuppressive doses of radiation (Hematopoietic Syndrome …
Detailed FDA approval information for Leukine, including regulatory status, product details, and official drug labeling information.
2024年12月6日 · LEUKINE is indicated for the treatment of adult and pediatric patients 2 years and older who have undergone allogeneic or autologous bone marrow transplantation in whom …
2024年12月15日 · LEUKINE is indicated to increase survival in adult and pediatric patients from birth to 17 years of age acutely exposed to myelosuppressive doses of radiation (Hematopoietic Syndrome …
Commercial-stage cancer biotech company, Partner Therapeutics, Inc. (PTx), announced the recent FDA approval of Leukine for the treatment of adult and pediatric patients acutely exposed to …
1 INDICATIONS AND USAGE LEUKINE is a leukocyte growth factor indicated: To shorten time to neutrophil recovery and to reduce the incidence of severe and life-threatening infections and …
2018年3月30日 · The FDA has approved the use of sargramostim (Leukine) to increase survival in adult and pediatric patients acutely exposed to myelosuppressive doses of radiation, known as …
2018年3月30日 · The Food and Drug Administration (FDA) has approved the use of Leukine (sargramostim; Sanofi Genzyme) to increase survival in children and adults exposed to …
2018年6月6日 · Leukine® (sargramostim) is indicated for the following uses: (i) following induction chemotherapy in older adult patients with acute myelogenous leukemia (AML) to shorten time to...
2018年6月6日 · The FDA approved sargramostim (Leukine) as a treatment for adult and pediatric patients with hematopoietic subsyndrome of acute radiation syndrome (H-ARS), which occurs …