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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 FDA Label - NDC 71837-5843

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 …

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Leukine - FDA Drug Approval Details

Detailed FDA approval information for Leukine, including regulatory status, product details, and official drug labeling information.

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Leukine: Package Insert / Prescribing Information / MOA

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 …

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SARGRAMOSTIM — FDA Drug Profile — RegDataLab

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 …

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FDA Approves Sargramostim for Hematopoeic Acute ...

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 …