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Neulasta
Pegfilgrastim
$460.00
6mg/0.6mL · 1 pre-filled syringe
GenericGeneric medicine· By UniPharm
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6mg/0.6mL
About Neulasta
Overview
Neulasta contains pegfilgrastim, a white blood cell growth factor supplied in a pre-filled syringe. It is used in adults and children with cancers that do not start in myeloid blood-forming cells to reduce infection associated with fever and low neutrophil counts during certain bone marrow-suppressing cancer treatments. It is also used to increase survival after acute exposure to radiation that suppresses bone marrow function. It works by stimulating blood-forming cells to grow, develop and become active.
What it treats
- To reduce infection associated with febrile neutropenia (fever with a low neutrophil count) in adults and children with non-myeloid cancers receiving bone marrow-suppressing anticancer drugs that carry a clinically significant risk of this complication. - To increase survival in adults and children acutely exposed to radiation that suppresses bone marrow function (the hematopoietic subsyndrome of acute radiation syndrome).
Safety information
Side effects
Common side effects include bone pain and pain in the arms or legs. Contact a doctor immediately if you develop pain in the upper left abdomen or shoulder, fever, breathing difficulties, or a serious allergic reaction. Neulasta can cause rupture of the spleen, which can be fatal; acute respiratory distress syndrome, a serious lung condition; and severe allergic reactions, including anaphylaxis. People with sickle cell disorders may develop sickle cell crises, which can be fatal. Other serious risks include kidney inflammation (glomerulonephritis), increased white blood cell counts, low platelet counts, capillary leak syndrome, and inflammation of large or medium-sized blood vessels. Platelet counts should be monitored during treatment. The label also warns of the potential for stimulating tumour growth. Patients with breast or lung cancer receiving Neulasta alongside chemotherapy and/or radiotherapy should be monitored for signs of myelodysplastic syndrome (MDS) and acute myeloid leukaemia (AML).
When to call your doctor
If symptoms are severe or getting worse quickly, seek emergency care rather than waiting.
Before taking this medicine
Do not use Neulasta if you have ever had a serious allergic reaction to pegfilgrastim or filgrastim, including anaphylaxis. Conditions requiring caution include sickle cell disease, because potentially fatal sickle cell crises can occur; kidney inflammation (glomerulonephritis); and low platelet counts, which require monitoring. Patients with breast or lung cancer receiving Neulasta alongside chemotherapy and/or radiotherapy should be monitored for myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). Seek urgent medical attention for left upper abdominal or shoulder pain, which may indicate an enlarged or ruptured spleen; fever or breathing difficulties, which need assessment for acute respiratory distress syndrome (ARDS); or signs of a serious allergic reaction. Splenic rupture can be fatal. Neulasta must be permanently stopped after a serious allergic reaction and stopped if ARDS or a sickle cell crisis occurs, or if inflammation of large or medium-sized arteries is suspected.
Using Neulasta
Dosing
Dosing is set by your prescriber. Each health care professional may prescribe medication differently according to a patient's medical history and condition, so follow the directions on your prescription label and speak to your doctor or pharmacist before changing anything.
Storage
Store in the original carton to protect it from light. Check the pack for whether it must be refrigerated before first use. Keep all medicines out of the sight and reach of children.
Clinical information on this page is summarised from the US FDA label NEULASTA (PEGFILGRASTIM) KIT NEULASTA (PEGFILGRASTIM) INJECTION NEULASTA (PEGFILGRASTIM) SOLUTION [AMGEN, INC] (DailyMed, retrieved 19 September 2026).
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