Active Ingredient: Sargramostim
Sargramostim is indicated for the acceleration of myeloid reconstitution in adult and pediatric patients 2 years of age and older undergoing allogeneic bone marrow transplantation from HLA-matched related donors.
For this indication, competent medicine agencies globally authorize below treatments:
For:
Intravenous, 250 micrograms sargramostim per square meter of body surface, once daily, over the duration of 3 days.
The recommended dose is 250 mcg/m²/day administered intravenously over a 2-hour period beginning two to four hours after bone marrow infusion, and not less than 24 hours after the last dose of chemotherapy or radiotherapy. Do not administer sargramostim until the post marrow infusion ANC is less than 500 cells/mm³. Continue sargramostim until an ANC greater than 1500 cells/mm³ for three consecutive days is attained. Do not administer sargramostim within 24 hours preceding or following receipt of chemotherapy or radiotherapy.
Obtain a CBC with differential twice per week during LEUKINE therapy and modify the dose as for the following:
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