What is Udenyca?
Udenyca is a form of a protein that stimulates the growth of white blood cells that help your body fight against infection.
Udenyca may also be used for purposes not listed in this medication guide.
Follow all directions on your medicine label and package. Tell each of your healthcare providers about all your medical conditions, allergies, and all medicines you use.
Before taking this medicine
Tell your doctor if you have ever had:
sickle cell disorder;
chronic myeloid leukemia;
myelodysplastic syndrome (also called "preleukemia"); or
a latex allergy.
Treatment with Fulphila and radiation with or without chemotherapy for breast or lung cancer, you could develop a blood disorder or blood cancer (leukemia). Ask your doctor about this risk.
Tell your doctor if you are pregnant or breastfeeding.
How should I use Udenyca?
Follow all directions on your prescription label and read all medication guides or instruction sheets. Use the medicine exactly as directed. Udenyca should not be given within 14 days before or 24 hours after you receive chemotherapy.
Udenyca is injected under the skin. A healthcare provider may teach you how to properly use the medication by yourself.
Read and carefully follow any Instructions for Use provided with your medicine. Ask your doctor or pharmacist if you don't understand all instructions.
Prepare your injection only when you are ready to give it. Do not use if the medicine looks cloudy, has changed colors, or has particles in it. Call your pharmacist for new medicine.
Carefully follow your doctor's instructions when giving Udenyca to a child who weighs less than 99 pounds (45 kilograms). The correct dose for a child this size cannot be accurately measured using the prefilled syringe.
You may need medical tests to help your doctor determine how long to treat you with Udenyca.
Store the prefilled syringe in its original package in the refrigerator, protected from light. Do not shake or freeze.
Take the syringe out of the refrigerator and let it reach room temperature for 15 to 30 minutes before injecting your dose. If a syringe has become frozen, thaw it in a refrigerator. Do not use any syringe that has been frozen more than one time.
Do not use a Neulasta or Udenyca syringe that has been left at room temperature for longer than 48 hours. Do not use a Fulphilaor Ziextenzo syringe that has been left at room temperature for longer than 72 hours.
The Neulasta Onpro Injector is a special device placed on the skin that delivers your Udenyca dose at a specific time. You will need to wear the device for 27 hours before the dose begins. The timed dose will then be released from the device slowly over a 45-minute period.
Keep Neulasta Onpro refrigerated until you are ready to wear it. Do not use an Onpro device that has been left out of a refrigerator for longer than 12 hours.
While wearing Neulasta Onpro, you or a caregiver will need to check the device to make sure it is working properly.
Each prefilled syringe or Onpro Injector is for one use only. Throw it away after one use, even if there is still medicine left inside.
Use a needle and syringe only once and then place them in a puncture-proof "sharps" container. Follow state or local laws about how to dispose of this container. Keep it out of the reach of children and pets.
What happens if I miss a dose?
Call your doctor for instructions if you miss an injection, or if you have a problem with the Neulasta Onpro device.
What happens if I overdose?
Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.
What should I avoid while using Udenyca?
When using Neulasta Onpro: Avoid traveling, driving, or operating machinery while wearing the device.
Udenyca side effects
Get emergency medical help if you have signs of an allergic reaction: hives, skin rash, sweating, warmth or tingly feeling; dizziness, fast heartbeats; wheezing, difficulty breathing; swelling of your face, lips, tongue, or throat.
Capillary leak syndrome is a rare but serious side effect of pegfilgrastim. Call your doctor right away if you have signs of this condition, which may include: decreased urination, tiredness, dizziness or light-headed feeling, trouble breathing, and sudden swelling, puffiness, or feeling of fullness.
Call your doctor at once if you have:
sudden or severe pain in your left upper stomach spreading up to your shoulder;
sudden and severe pain in your chest, stomach, or back;
severe or ongoing pain anywhere in your body;
shortness of breath, rapid breathing;
pale skin, easy bruising, unusual bleeding;
bruising, swelling, or a hard lump where the medicine was injected; or
kidney problems--little or no urination, pink or dark urine, swelling in your face or lower legs.
Your cancer treatments may be delayed or permanently discontinued if you have certain side effects.
Common side effects may include:
bone pain; or
pain in your arms or legs.
This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
What other drugs will affect Udenyca?
Other drugs may affect Udenyca, including prescription and over-the-counter medicines, vitamins, and herbal products. Tell your doctor about all your current medicines and any medicine you start or stop using.
Frequently asked questions
- Why do you take Claritin with Neulasta?
- How many biosimilars have been approved in the United States?
- Does Neulasta cause bone pain?
- How long do the side effects of the Neulasta (pegfilgrastim) shot last?
- When can I remove the Neulasta Onpro?
- When does Neulasta reach peak levels?
- How do you increase white blood cells during chemo?
More about Udenyca (pegfilgrastim)
- Side Effects
- During Pregnancy
- Dosage Information
- Drug Interactions
- Pricing & Coupons
- En Español
- 3 Reviews
- Drug class: colony stimulating factors
- FDA Approval History
Related treatment guides
Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed.
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
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