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ACTEMRA (tocilizumab) | Rheumatoid Arthritis Treatment
Learn about ACTEMRA® (tocilizumab), a prescription medicine used to treat adults with moderate to severe rheumatoid arthritis (RA). ACTEMRA is a prescription medicine called an interleukin- 6 (IL-6) receptor inhibitor. ACTEMRA is used to treat adults with moderately to severely active rheumatoid arthritis. ACTEMRA can lower the ability of your immune system to fight infections. Some people have serious infections while taking ACTEMRA, including tuberculosis (TB), and infections caused by bacteria, fungi, or viruses that can spread throughout the body. Some people have died from these infections. Other serious side effects of ACTEMRA include tears (perforation) of the stomach and intestines, changes in blood test results (including low neutrophil count, low platelet count, increase in certain liver function tests, and increase in blood cholesterol levels), hepatitis B infection becoming an active infection again, and nervous system problems. Serious allergic reactions, including death, can happen with ACTEMRA. These reactions may happen with any infusion of ACTEMRA, even if they did not occur with an earlier infusion. Common side effects with ACTEMRA in patients with RA include upper respiratory tract infections (common cold, sinus infections), headache, and increased blood pressure (hypertension). Tell your healthcare provider if you have any side effect that bothers you or that does not go away. These are not all of the possible side effects of ACTEMRA. For more information, ask your healthcare provider or pharmacist. Do not take ACTEMRA if you are allergic to tocilizumab, or any of the ingredients in ACTEMRA. Patients must tell their healthcare provider if they plan to become pregnant or are pregnant. It is not known if ACTEMRA will harm an unborn baby. Genentech has a registry for pregnant women who take ACTEMRA. Patients who are pregnant or become pregnant while taking ACTEMRA must contact the registry at 1-877-311-8972 and talk to their healthcare provider. Patients must call their healthcare provider for medical advice about any side effects. Patients are encouraged to report side effects to Genentech and the FDA. Patients may contact Genentech by calling 1-888-835-2555. Patients may contact the FDA by visiting www.fda.gov/medwatch or calling 1-800- FDA-1088.
ra, rheumatoid arthritis, actemra, tocilizumab, biologic, dmard, ra treatment, interleukin-6, il-6, rheumatoid arthritis treatment, rheumatologist, severe ra, moderate to severe ra
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