Click here to view the indications and important safety information, including Boxed Warnings, for Rituxan and ACTEMRA.
Thank you for your interest in the Genentech Rheumatology Co-pay Card Program. If you are a patient taking Rituxan or ACTEMRA, please select your medication below to get started. If you are a health care provider, please select "I’m a health care provider."
Rheumatoid arthritis (RA): with another prescription medicine called methotrexate, to reduce the signs and symptoms of moderate to severe active RA in adults, after treatment with at least one other medicine called a tumor necrosis factor (TNF) antagonist has been used and did not work well enough.
Granulomatosis with Polyangiitis (GPA) (Wegener's Granulomatosis) and Microscopic Polyangiitis (MPA): with glucocorticoids, to treat GPA and MPA.
People with serious infections should not receive Rituxan. It is not known if Rituxan is safe or effective in children.
Rituxan can cause serious side effects that can lead to death, including:
What are the possible side effects of Rituxan?
Rituxan can cause serious and life-threatening side effects, including:
What are common side effects during treatment with Rituxan?
Other side effects include:
You may report side effects to the FDA at (800) FDA-1088 or www.FDA.gov/medwatch. You may also report side effects to Genentech at (888) 835-2555.
ACTEMRA is a prescription medicine called an interleukin-6 (IL-6) receptor antagonist. ACTEMRA is used to treat:
ACTEMRA can cause serious side effects.
ACTEMRA changes the way your immune system works. This can make you more likely to get infections or make any current infection worse. Some people taking ACTEMRA have died from these infections.
ACTEMRA can cause other serious side effects including stomach tears; changes in blood test results that check for low neutrophil and platelet counts, and increases in certain liver function test levels and blood cholesterol levels; increased risk of certain cancers by changing the way your immune system works; hepatitis B infection; serious allergic reactions, including death (these may happen with ACTEMRA infusions or injections, even if they did not occur with an earlier infusion or injection); and nervous system problems.
Tell your doctor if you're allergic to ACTEMRA or if you've had a bad reaction to ACTEMRA previously.
Common side effects in patients with RA include upper respiratory tract infections (like common cold and sinus infections), headache, increased blood pressure (also called hypertension), and injection site reactions. Tell your doctor if you have these or any other side effect that bothers you or does not go away.
Common side effects in patients with PJIA or SJIA include upper respiratory tract infections (common cold, sinus infections), headache, and diarrhea.
Tell your doctor if you are planning to become pregnant, are pregnant, plan to breast-feed, or are breast-feeding. You and your doctor should decide if you will take ACTEMRA or breast-feed. You should not do both. If you are pregnant and taking ACTEMRA, join the pregnancy registry. To learn more, call 1-877-311-8972 or talk to your doctor to register.
Tell your doctor right away if you are experiencing any side effects. You may report side effects to the FDA at 1-800-FDA-1088 or www.FDA.gov/medwatch. You may also call Genentech at 1-888-835-2555.
Rituxan® and its logo are registered trademarks of Biogen Idec, Inc.
ACTEMRA® and its logo are registered trademarks of Chugai Seiyaku Kabushiki Kaisha Corp., a member of the Roche Group.
The Rituxan Prepaid MasterCard and ACTEMRA Prepaid MasterCard are issued by The Bancorp Bank pursuant to license by MasterCard International Incorporated. MasterCard is a registered trademark of MasterCard International Incorporated. These cards may not be used everywhere Debit MasterCard is accepted. No cash or ATM access. The Bancorp Bank; Member FDIC.