Pronounce: fil-GRA-stim
Classification: Colony Stimulating Factor
Filgrastim is a type of colony stimulating factor, which is a group of medications that stimulate the production and function of blood cells. Granulocyte colony-stimulating factor (G-CSF) is a protein naturally produced by the body to increase the production of white blood cells. Filgrastim is a man-made version of G-CSF that stimulates white blood cell production, and in particular, neutrophil production. A neutrophil is a type of white blood cell that is responsible for fighting infection and is often decreased during cancer therapy. When the number of these cells drops below 1000/mm3, it is called neutropenia, which puts the patient at significant risk of infection. Filgrastim is used to prevent neutropenia related to cancer therapy. It may also be used to increase the number of white blood cells prior to a stem cell collection for transplant.
Filgrastim is not a cancer treatment, but a supportive care medicine. This means it is used to lessen bone marrow suppression (reduced blood counts) secondary to cancer and its cytotoxic treatments.
Filgrastim is most often given as a subcutaneous injection (SQ, given under the skin), but it can be given directly into a vein (intravenous, IV). It is given once a day, preferably at the same time of day, until the neutrophil count returns to normal. The actual dose is based on your body size and what you are taking it for and will be determined by your healthcare provider.
Because this medication works to increase your white blood cell count, you will have your blood cell count monitored to ensure that your white blood cell count does not become too high.
The needle cap on the prefilled syringes is made with dry, natural rubber which is derived from latex. If you have a latex allergy, it is important to notify your care provider to determine the safest way for you to receive your filgrastim.
Filgrastim should be stored in the refrigerator and in the original carton to protect it from light. To lessen the sting of the injection, it should be taken out of the refrigerator 30 minutes prior to being injected. Filgrastim should be started no sooner than 24 hours after completion of the chemotherapy dose.
Do not reuse single-dose vials, syringes, or needles. Do not throw the vials, syringes, or needles in the household trash. Dispose of all used needles and syringes in a puncture-proof disposable container with a lid. The FDA provides further information about the disposal of vials, syringes and needles.
Depending on your insurance coverage, filgrastim is available through specialty, retail, or mail order pharmacies. Your oncology team will work with your prescription drug plan to identify an in-network pharmacy for medication distribution.
Alternatively, this medication may be given in the doctor’s office, clinic, or infusion suite. Where you receive it is often dependent on your insurance coverage.
This medication may be covered under your major medical plan or prescription drug plan. Patient assistance may be available to qualifying individuals depending upon prescription drug coverage. Co-pay cards, which reduce the patient co-pay responsibility for eligible commercially (non-government sponsored) insured patients, may also be available. Your care team can help you find these resources, if they are available.
There are a number of things you can do to manage the side effects of filgrastim. Talk to your care team about these recommendations. They can help you decide what will work best for you. These are some of the most common or important side effects:
Filgrastim stimulates the bone marrow to produce many white blood cells, which can lead to pain in the bones. This pain is often felt in the bones of the thighs, hips, and upper arms. Your healthcare team may not want you to take acetaminophen (Tylenol™) because it can "mask" a fever, so talk to them about which pain relievers you can safely take. Anti-histamines like loratidine (Claritin) may help lessen bone pain. Ask your provider or pharmacist if you should take this or any other medications to help manage this side effect.
Some people experience redness, swelling, or itching at the site of injection. This is usually temporary. The injection is known to sting or burn if given when it is cold. Take the medication out of the refrigerator 30 minutes ahead of time to allow it to come up to room temperature before administration. Rotate the sites that the injection is given, inject slowly, and/or numb the area with ice prior to giving the injection.
Platelets help your blood clot, so when the count is low you are at a higher risk of bleeding. Let your oncology care team know if you have any excess bruising or bleeding, including nose bleeds, bleeding gums or blood in your urine or stool. If the platelet count becomes too low, you may receive a transfusion of platelets.
It is not known if exposure of an unborn child to this medication could cause birth defects, so you should not become pregnant or father a child while on this medication. Effective birth control is necessary during treatment. Even if your menstrual cycle stops or you believe you are not producing sperm, you could still be fertile and conceive. You should consult with your healthcare team before breastfeeding while receiving this medication.
There are biosimilar versions of filgrastim. A biosimilar is a medication that has been approved by the FDA because it is very similar to an FDA-approved medication (called a reference product, or the medication it is being compared to), and that there are no meaningful differences between the biosimilar product and the reference product. These medications may be used interchangeably.
The current biosimilar versions of this medication include filgrastim-sndz (Zarxio®) and filgrastim-aafi (Nivestym™).
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