Anthropometric Measurements as Predictors of Low Birth Weight Among Tanzanian Neonates: A Hospital-Based Study
November 7, 2025
Brand Name :
Neupogen, Nivestym, Zarxio, Releuko, Granix, Zarxio
Synonyms :
filgrastim   
Class :
Hematopoietic Growth Factors
Dosage Forms & Strengths  Â
Prefilled syringe for subcutaneous (injectable solution)Â
300mcg/0.5mlÂ
480mcg/0.8ml Â
Neupogen, Zarxio, Releuko, Granix, NivestymÂ
10 mcg/kg Intravenous infusion over 4 to 24 hours after BMT daily (24-hour infusion is maximum)
After cytotoxic chemotherapy and at least one day after a bone marrow infusion, give the first dosage.
Dose titration
If ANC falls below 1000mm3 at any point while taking 5 mcg/kg daily, up the dosage to 10 mcg/kg daily, and then proceed.
Dosage Forms & Strengths  Â
Prefilled syringe for subcutaneous (injectable solution)Â
300mcg/0.5mlÂ
480mcg/0.8ml Â
Neupogen, Zarxio, Releuko, Granix, NivestymÂ
Autologous Peripheral Blood Progenitor Cell MobilizationÂ
10%/kg/day subcutaneous
Start 4 days prior to leukapheresis and continue through the final day of leukapheresis
Patients with Cancer Undergoing Bone Marrow Transplantation
10 mcg/kg intravenous infusion per day
Give the first dosage 24 hours after receiving cytotoxic chemotherapy and 24 hours after receiving bone marrow infusion
Dosage adjustment
Decrease to 5 mcg/kg/day when ANC is more than 1000/mm3 for three days in a row
If the ANC stays above 1000 mm3 on three more days in a row: Stop providing
Then, if ANC falls to less than 1000/mm3: Continue at 5 mcg/kg/day
Refer to adult dosingÂ
it may increase the adverse effect when combined with aldesleukin
sipuleucel-T: they may decrease the therapeutic effect of immunostimulants
leflunomide: they may increase the immunosuppressive effect of immunostimulants
denosumab: they may increase the immunosuppressive effect of immunostimulants
baricitinib: they may enhance the immunosuppressive effect of immunostimulants
filgrastim: they may increase the immunosuppressive effect of selective immunosuppressants
filgrastim: they may increase the immunosuppressive effect of selective immunosuppressants
filgrastim: they may increase the immunosuppressive effect of selective immunosuppressants
may increase the immunosuppressive effect of Immunosuppressive agents
may enhance the serum concentration when combined
cladribine: they may increase the immunosuppressive effect of immunostimulants
deucravacitinib: they may increase the immunosuppressive effect of immunostimulants
immunostimulants: they may increase the toxic effect of nadofaragene firadenovec
natalizumab: they may increase the immunosuppressive effect of immunostimulants
pimecrolimus: they may increase the immunosuppressive effect of immunostimulants
ruxolitinib: they may increase the immunosuppressive effect of immunostimulants
talimogene laherparepvec: they may increase the toxic effect of immunostimulants
tofacitinib: they may increase the immunosuppressive effect of immunostimulants
upadacitinib: they may increase the immunosuppressive effect of immunostimulants
antithymocyte globulin equineÂ
antithymocyte globulin: they may increase the toxic effect of immunostimulants
abrocitinib: they may increase the immunosuppressive effect of immunostimulants
yellow fever vaccine: they may increase the toxic effect of immunostimulants
when both drugs are combined, there may be increased myelosuppressive activities of filgrastim.   
when both the drugs are combined, carmustine increases the myelosuppressive effects of filgrastim    
brincidofovir: they may decrease the therapeutic effect of immunostimulants
inebilizumab: they may increase the immunosuppressive effect of immunostimulants
ocrelizumab: they may increase the immunosuppressive effect of immunostimulants
ofatumumab: they may increase the immunosuppressive effect of immunostimulants
pidotimod: they may decrease the therapeutic effect of immunostimulants
ublituximab: they may increase the immunosuppressive effect of immunostimulants
Actions and Spectrum:Â
filgrastim works by attaching to certain receptors on the surface of bone marrow cells, which stimulates the proliferation and differentiation of those cells into white blood cells. As a result, the amount of neutrophils in the circulation rises, aiding in the battle against infections and other conditions that might cause neutropenia (low levels of neutrophils).Â
The spectrum of filgrastim refers to the variety of problems that the medicine can be used to treat. It is primarily used to prevent or cure neutropenia induced by chemotherapy or radiation therapy in individuals with cancer. Moreover, it can be used to treat neutropenia in individuals with additional illnesses such HIV infection, severe persistent neutropenia, and bone marrow transplantation.Â
Frequency Defined Â
>10%Â
Vomiting (57%)Â
Alopecia (18%)Â
Nausea (57%)Â
Fever (12%)Â
Bone pain (22%-33%)Â
Fatigue (11%)Â
Diarrhea (14%)Â
1-10%Â
AnorexiaÂ
DyspneaÂ
Chest painÂ
ConstipationÂ
Sore throatÂ
StomatitisÂ
RashÂ
HeadacheÂ
CoughÂ
Post marketing reportsÂ
Splenic ruptureÂ
GlomerulonephritisÂ
Alveolar hemorrhage and hemoptysisÂ
cutaneous vasculitisÂ
Sweet syndrome (acute febrile neutrophilic dermatosis)Â
Decreased bone density and osteoporosis in children with severe chronic neutropenia receiving long-term treatmentÂ
Respiratory distress syndromeÂ
Myelodysplastic syndromeÂ
Acute myeloid leukemiaÂ
Capillary leak syndromeÂ
AortitisÂ
Sickle cell crisisÂ
ARDSÂ
AstheniaÂ
Frequency not definedÂ
Elevated alkaline phosphataseÂ
Elevated uric acidÂ
Elevated lactate dehydrogenaseÂ
Black Box WarningÂ
A black box warning for filgrastim mentions the possibility of splenic rupture, a potentially fatal disease where the spleen may burst or rupture.Â
Healthcare professionals are urged by the black box warning to keep an eye out for symptoms of splenic rupture in patients using filgrastim, such as left upper abdomen or shoulder discomfort. filgrastim should be stopped right away if splenic rupture is suspected.Â
Contraindication/Caution:Â
Contraindication:Â
Caution:Â
Pregnancy warnings:    Â
Pregnancy category: N/AÂ
Lactation: Excretion into human milk is knownÂ
Pregnancy Categories:        Â
Category A: Studies that were well-controlled and met expectations revealed no risk to the fetus in either the first or second trimester.Â
Category B: There were lack of studies on pregnant women and no evidence of risk to the foetus in animal experiments.  Â
Category C: there was evidence of risk of adverse effects in animal reproduction studies, and no adequate evidence in human studies must take care of potential risks in pregnant women.   Â
Category D: adequate data available with sufficient evidence of human fetal risk from various platforms, but despite the potential risk, and used only in emergency cases for potential benefits.  Â
Category X: Drugs listed in this category outweigh the risks over benefits. Hence these categories of drugs need to be avoided by pregnant women.   Â
Category N: There is no data available for the drug under this category
PharmacologyÂ
A recombinant human substance called filgrastim, also known as granulocyte colony-stimulating factor (G-CSF), encourages the production of neutrophils, a kind of white blood cell, in the bone marrow. It is a glycoprotein that is created using recombinant DNA technology in Escherichia coli bacteria.Â
PharmacodynamicsÂ
By attaching to certain receptors on the surface of neutrophil progenitor cells, filgrastim increases the growth, differentiation, and maturation of these progenitor cells into adult neutrophils. The medication also improves mature neutrophil survival and performance, including their capacity to go to infection sites and phagocytose pathogens.Â
PharmacokineticsÂ
Absorption  Â
filgrastim is delivered through subcutaneous injection or intravenous infusion. The subcutaneous mode of administration leads in slower absorption than the intravenous approach. When taken subcutaneously, filgrastim has a bioavailability of 60 to 70%.Â
DistributionÂ
With a volume of distribution of around 150 mL/kg, filgrastim is most likely to be found in the extracellular fluid compartment. The medication does not bind appreciably to plasma proteins.Â
MetabolismÂ
filgrastim is not metabolized by the liver or other organs. It is largely removed by the kidneys.Â
Elimination and excretionÂ
filgrastim is mostly removed through renal excretion. In healthy people, filgrastim has an elimination half-life of around 3–4 hours. The elimination half-life may be extended in individuals with poor renal function, and dosage changes may be required.Â
Administration: Â
filgrastim is commonly delivered by subcutaneous injection or intravenous infusion.Â
The recommended dosage of filgrastim, given as an intravenous infusion or subcutaneous injection, is 5 mcg/kg of body weight per day for the treatment of chemotherapy-induced neutropenia in patients with non-myeloid malignancies.Â
Patient information leafletÂ
Generic Name: filgrastim   Â
Why do we use filgrastim?Â
filgrastim is a medication used to increase the production of neutrophils, a type of white blood cell, in the bone marrow.Â
Patients receiving chemotherapy for cancer can use filgrastim to prevent or lessen the occurrence and severity of neutropenia (low white blood cell count).Â
filgrastim is used to increase the formation of stem cells in the bone marrow and enhance regeneration of donor cells in patients undergoing bone marrow transplantation.Â