Description
Ruxience (rituximab-pvvr) is a medication that is given via an intravenous (IV) infusion to treat adults with non-Hodgkin's Lymphoma, chronic lymphocytic leukemia, rheumatoid arthritis, or granulomatosis with polyangiitis and microscopic polyangiitis.
Fact Table
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Formula
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C6416H9874N1688O1987S44
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License
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US FDA, EMA
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Bioavailability
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Not applicable (IV administration)
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Legal status
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Prescription only (Rx)
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Chemical Name
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Rituximab
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Elimination half-life
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18 days
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Dosage (Strength)
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100 mg/10 mL, 500 mg/50 mL
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Pregnancy
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Consult a doctor
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Brands
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Ruxience, Rituxan, MabThera, Truxima
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Protein binding
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Not reported
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PubChem CID
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50943701
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MedlinePlus
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a607038
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ChEBI
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CHEBI:134722
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ATC code
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L01XC02
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DrugBank
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DB00073
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KEGG
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D02995
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Routes of administration
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Intravenous (IV)
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Directions
Your doctor will determine an appropriate treatment regimen for you. Ruxience will be administered via an IV infusion by a healthcare professional. Inform your doctor of any questions or concerns you may have about the medication.
Ingredients
The active ingredient in Ruxience is rituximab-pvvr.
Inactive ingredients include edetate disodium dihydrate, L-histidine, L-histidine hydrochloride monohydrate, polysorbate 80, sucrose, and Water for Injection.
Contraindications
There are no contraindications to Ruxience per the most recent Prescribing Information.
Cautions
- Ruxience contains the following FDA Boxed Warning:
- Infusion-related reactions that can be fatal may occur within 24 hours of rituximab infusion; approximately 80% of fatal reactions occurred with first infusion. Patients should be monitored, and Ruxience should be stopped if severe reactions occur.
- Severe mucocutaneous reactions can occur, which may be fatal.
- Reactivation of hepatitis B virus (HBV) that may result in fulminant liver inflammation, liver failure, and death can occur.
- Progressive multifocal leukoencephalopathy (PML) may occur and can result in death.
- Before you begin treatment with Ruxience, inform your doctor of:
- All the prescription and over-the-counter medications you take
- Your allergies
- Your current health problems and past medical history
- Your pregnancy or breastfeeding status
- Ruxience is associated with the following warnings and precautions:
- Tumor lysis syndrome
- Infections
- Cardiac adverse reactions
- Kidney problems
- Bowel obstruction and perforation
- Harm to an unborn baby. Effective contraception is recommended for females of childbearing age during treatment with Ruxience and for 12 months after the final dose.
- Breastfeeding is not recommended.
- Live vaccines should not be administered to patients receiving Ruxience.
Side Effects
Infusion-related reactions, fever, decreased lymphocytes, chills, infection, weakness, upper respiratory tract infections, nasopharyngitis, urinary tract infections, bronchitis, nausea, diarrhea, headache, muscle spasms, anemia, and swelling are common Ruxience side effects; however, other side effects may also occur. Immediately inform your doctor of any side effects that bother you or won’t go away.
Ask your doctor about Ruxience.
Reference
Ruxience. New York, NY: Pfizer Labs; 2023.
About Dr. Savannah Muncy (Page Author)
Dr. Muncy (PharmD) studied science and education as an undergraduate before attending the Appalachian College of Pharmacy where she completed her PharmD in three years. She is currently using her pharmacy and healthcare expertise to write medical content for clients all around the world. She is focused on delivering the most current, accurate, and engaging information to healthcare professionals and patients. Read More....
IMPORTANT NOTE:
The above information is intended to increase awareness of health information and does not suggest treatment or diagnosis. This information is not a substitute for individual medical attention and should not be construed to indicate that use of the drug is safe, appropriate, or effective for you. See your health care professional for medical advice and treatment.
Product Code : 14560