Rasburicase
Generic name: rasburicase [ ras-BUR-ih-kase ]
Brand names: Elitek, Fasturtec, Fasturtec(obs)
Dosage form: intravenous powder for injection (1.5 mg; 7.5 mg)
Drug class: Antihyperuricemic agents
What is rasburicase?
Rasburicase is used to manage uric acid levels in adults and children receiving cancer treatment for leukemia, lymphoma, and certain tumors.
Rasburicase may also be used for purposes not listed in this medication guide.
Rasburicase side effects
Get emergency medical help if you have signs of an allergic reaction: hives, rash; wheezing, chest pain and tightness, difficult breathing; feeling light-headed; swelling of your face, lips, tongue, or throat.
Tell your caregivers or call your doctor at once if you have:
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pale or yellowed skin, dark colored urine;
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sores or white patches in or around your mouth, trouble swallowing or talking, dry mouth, bad breath, altered sense of taste;
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fever, flu symptoms, rapid heart rate, rapid and shallow breathing, fainting; or
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signs of a serious blood disorder--blue-colored skin or lips, headache, feeling weak or tired, trouble breathing, feeling like you might pass out, pounding heartbeats or fluttering in your chest.
Your treatment with rasburicase may be permanently discontinued if you have a serious allergic reaction.
Common side effects of rasburicase may include:
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headache;
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abnormal liver function tests, decreased phosphate levels;
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throat pain;
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fever; or
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swelling in your hands or feet.
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.
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Warnings
You should not receive rasburicase if you have ever had an allergic reaction or blood cell problems after receiving rasburicase, or if you have a genetic enzyme deficiency called glucose-6-phosphate dehydrogenase (G6PD) deficiency.
Get emergency medical help if you have signs of an allergic reaction: hives; wheezing, chest pain and tightness, difficult breathing; feeling light-headed; swelling of your face, lips, tongue, or throat.
Tell your caregivers or call your doctor at once if you have signs of a serious blood disorder--blue-colored skin or lips, headache, feeling weak or tired, trouble breathing, feeling like you might pass out, pounding heartbeats or fluttering in your chest.
Before taking this medicine
You should not receive this medicine if:
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you have ever had an allergic reaction or blood cell problems after receiving rasburicase; or
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you have an enzyme deficiency called glucose-6-phosphate dehydrogenase deficiency (G6PD).
If you are of African or Mediterranean descent, your doctor may perform blood tests to make sure you do not have conditions that would prevent you from safely receiving rasburicase.
Rasburicase may harm an unborn baby. Use effective birth control to prevent pregnancy, and tell your doctor if you become pregnant.
Do not breastfeed while using this medicine, and for at least 2 weeks after your last dose.
Rasburicase is not approved for use by anyone younger than 1 month old.
How is rasburicase given?
Rasburicase is given as an infusion into a vein. A healthcare provider will give you this injection.
rasburicase must be given slowly, and the infusion can take at least 30 minutes to complete.
Rasburicase is usually given once per day for up to 5 days. Follow your doctor's dosing instructions very carefully.
While using rasburicase, you may need frequent blood tests.
This medicine can affect the results of certain medical tests. Tell any doctor who treats you that you are using rasburicase.
Rasburicase dosing information
Usual Adult Dose for Hyperuricemia Secondary to Chemotherapy:
0.2 mg/kg as a 30-minute IV infusion once a day for up to 5 days
Comments:
-Use beyond 5 days or administration of more than 1 course of therapy is not recommended
-The exact duration should be based upon adequate monitoring of uric acid levels in plasma and clinical judgement.
-This drug is only approved for a single course of treatment.
Use: For the initial management of plasma uric acid levels in patients with leukemia, lymphoma, and solid tumor malignancies who are receiving chemotherapy expected to result in tumor lysis and subsequent elevation of plasma uric acid.
Usual Pediatric Dose for Hyperuricemia Secondary to Chemotherapy:
0.2 mg/kg as a 30-minute IV infusion once a day for up to 5 days
Comments:
-Use beyond 5 days or administration of more than 1 course of therapy is not recommended.
-The exact duration should be based upon adequate monitoring of uric acid levels in plasma and clinical judgement.
-This drug is only approved for a single course of treatment.
Use: For the initial management of plasma uric acid levels in patients with leukemia, lymphoma, and solid tumor malignancies who are receiving chemotherapy expected to result in tumor lysis and subsequent elevation of plasma uric acid
What happens if I miss a dose?
Call your doctor for instructions if you miss an appointment for your rasburicase injection.
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 receiving rasburicase?
Follow your doctor's instructions about any restrictions on food, beverages, or activity.
What other drugs will affect rasburicase?
Other drugs may affect rasburicase, 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.
Rasburicase Biosimilars
Biosimilar and interchangeable products are biological products that are highly similar to and have no clinically meaningful differences from the reference product.
Reference products
These are biological products that have already been approved by the FDA, against which biosimilar products are compared. There is 1 for rasburicase.
Elitek (rasburicase) - Sanofi-Aventis U.S. LLC
Formulation type | Strength |
---|---|
Single-Dose Vial | 1.5 mg |
Single-Dose Vial | 7.5 mg |
View Elitek information in detail.
More about rasburicase
- Check interactions
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- Side effects
- Dosage information
- During pregnancy
- Drug class: antihyperuricemic agents
- Breastfeeding
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Further information
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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