Site Map | ACTEMRA® (tocilizumab)

www.actemra.com Review:

http://serenityhomedics.com/w/www.actemra.com.html

Rheumatoid Arthritis Treatment | ACTEMRA® (tocilizumab) - Learn about ACTEMRA® (tocilizumab), a prescription medicine used to treat moderate to severe rheumatoid arthritis and find patient support. IMPORTANT SAFETY INFORMATION-RA: ACTEMRA is a prescription medicine called an interleukin-6 (IL-6) receptor antagonist. ACTEMRA is used to treat adults with moderately to severely active rheumatoid arthritis (RA) after at least one other medicine called a disease modifying antirheumatic drug (DMARD) has been used and did not work well. 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; if you had hives, a rash, or experienced flushing after injecting, you should tell your doctor or nurse before your next injection); and nervous system problems. Tell your doctor if you're allergic to ACTEMRA or if you've had a reaction to ACTEMRA previously. Common side effects 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. 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. Please see full Prescribing Information, including Medication Guide and Serious Side Effects, for more Important Safety Information.

https://www.actemra.com/es/ra.html Rheumatoid Arthritis Treatment | ACTEMRA® (tocilizumab) - Learn about ACTEMRA® (tocilizumab), a prescription medicine used to treat moderate to severe rheumatoid arthritis and find patient support.

https://www.actemra.com/pjia.html Polyarticular Juvenile Idiopathic Arthritis | ACTEMRA® (tocilizumab) - Learn about ACTEMRA® (tocilizumab), an FDA approved medication for thetreatment of polyarticular juvenile idiopathic arthritis (PJIA) in patients 2 yearsof age & up. IMPORTANT SAFETY INFORMATION-RA: ACTEMRA is a prescription medicine called an interleukin-6 (IL-6) receptor antagonist. ACTEMRA is used to treat adults with moderately to severely active rheumatoid arthritis (RA) after at least one other medicine called a disease modifying antirheumatic drug (DMARD) has been used and did not work well. 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; if you had hives, a rash, or experienced flushing after injecting, you should tell your doctor or nurse before your next injection); and nervous system problems. Tell your doctor if you're allergic to ACTEMRA or if you've had a reaction to ACTEMRA previously. Common side effects 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. 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. Please see full Prescribing Information, including Medication Guide and Serious Side Effects, for more Important Safety Information.

https://www.actemra.com/sjia.html Systemic Juvenile Idiopathic Arthritis | ACTEMRA® (tocilizumab) - Learn about ACTEMRA® (tocilizumab), an FDA approved medication for thetreatment of systemic juvenile idiopathic arthritis (SJIA) in patients 2 years ofage & up. IMPORTANT SAFETY INFORMATION-RA: ACTEMRA is a prescription medicine called an interleukin-6 (IL-6) receptor antagonist. ACTEMRA is used to treat adults with moderately to severely active rheumatoid arthritis (RA) after at least one other medicine called a disease modifying antirheumatic drug (DMARD) has been used and did not work well. 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; if you had hives, a rash, or experienced flushing after injecting, you should tell your doctor or nurse before your next injection); and nervous system problems. Tell your doctor if you're allergic to ACTEMRA or if you've had a reaction to ACTEMRA previously. Common side effects 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. 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. Please see full Prescribing Information, including Medication Guide and Serious Side Effects, for more Important Safety Information.

https://www.actemra.com/ra/consider-actemra.html How ACTEMRA® RA Treatment Works Differently - Learn about how ACTEMRA® (tocilizumab) works differently to treat moderate to severe rheumatoid arthritis and find support for living with RA. IMPORTANT SAFETY INFORMATION-RA: ACTEMRA is a prescription medicine called an interleukin-6 (IL-6) receptor antagonist. ACTEMRA is used to treat adults with moderately to severely active rheumatoid arthritis (RA) after at least one other medicine called a disease modifying antirheumatic drug (DMARD) has been used and did not work well. 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; if you had hives, a rash, or experienced flushing after injecting, you should tell your doctor or nurse before your next injection); and nervous system problems. Tell your doctor if you're allergic to ACTEMRA or if you've had a reaction to ACTEMRA previously. Common side effects 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. 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. Please see full Prescribing Information, including Medication Guide and Serious Side Effects, for more Important Safety Information.

https://www.actemra.com/ra/consider-actemra/actemra-works-alone.html ACTEMRA® (tocilizumab) for RA without Methotrexate - Learn how ACTEMRA can be taken without disease modifying antirheumatic drugs like methotrexate to avoid unwanted side effects. IMPORTANT SAFETY INFORMATION-RA: ACTEMRA is a prescription medicine called an interleukin-6 (IL-6) receptor antagonist. ACTEMRA is used to treat adults with moderately to severely active rheumatoid arthritis (RA) after at least one other medicine called a disease modifying antirheumatic drug (DMARD) has been used and did not work well. 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; if you had hives, a rash, or experienced flushing after injecting, you should tell your doctor or nurse before your next injection); and nervous system problems. Tell your doctor if you're allergic to ACTEMRA or if you've had a reaction to ACTEMRA previously. Common side effects 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. 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. Please see full Prescribing Information, including Medication Guide and Serious Side Effects, for more Important Safety Information.

https://www.actemra.com/ra/consider-actemra/actemra-RA-patient-stories.html ACTEMRA® (tocilizumab) RA Patient Stories - Watch videos where patients talk about living with rheumatoid arthritis and how those taking ACTEMRA have been able to find better RA symptom relief. IMPORTANT SAFETY INFORMATION-RA: ACTEMRA is a prescription medicine called an interleukin-6 (IL-6) receptor antagonist. ACTEMRA is used to treat adults with moderately to severely active rheumatoid arthritis (RA) after at least one other medicine called a disease modifying antirheumatic drug (DMARD) has been used and did not work well. 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; if you had hives, a rash, or experienced flushing after injecting, you should tell your doctor or nurse before your next injection); and nervous system problems. Tell your doctor if you're allergic to ACTEMRA or if you've had a reaction to ACTEMRA previously. Common side effects 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. 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. Please see full Prescribing Information, including Medication Guide and Serious Side Effects, for more Important Safety Information.

https://www.actemra.com/ra/actemra-results.html ACTEMRA® (tocilizumab) for RA - SC Injection Benefits - Learn how ACTEMRA subcutaneous injection reduced RA symptoms in clinical trials for moderate to severe rheumatoid arthritis (RA). IMPORTANT SAFETY INFORMATION-RA: ACTEMRA is a prescription medicine called an interleukin-6 (IL-6) receptor antagonist. ACTEMRA is used to treat adults with moderately to severely active rheumatoid arthritis (RA) after at least one other medicine called a disease modifying antirheumatic drug (DMARD) has been used and did not work well. 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; if you had hives, a rash, or experienced flushing after injecting, you should tell your doctor or nurse before your next injection); and nervous system problems. Tell your doctor if you're allergic to ACTEMRA or if you've had a reaction to ACTEMRA previously. Common side effects 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. 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. Please see full Prescribing Information, including Medication Guide and Serious Side Effects, for more Important Safety Information.

https://www.actemra.com/ra/actemra-results/actemra-results-iv-infusion.html ACTEMRA® (tocilizumab) for RA - IV Infusion Benefits - Learn how ACTEMRA intravenous (IV) infusions helped RA symptoms in 5 clinical trials for moderate to severe rheumatoid arthritis (RA). IMPORTANT SAFETY INFORMATION-RA: ACTEMRA is a prescription medicine called an interleukin-6 (IL-6) receptor antagonist. ACTEMRA is used to treat adults with moderately to severely active rheumatoid arthritis (RA) after at least one other medicine called a disease modifying antirheumatic drug (DMARD) has been used and did not work well. 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; if you had hives, a rash, or experienced flushing after injecting, you should tell your doctor or nurse before your next injection); and nervous system problems. Tell your doctor if you're allergic to ACTEMRA or if you've had a reaction to ACTEMRA previously. Common side effects 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. 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. Please see full Prescribing Information, including Medication Guide and Serious Side Effects, for more Important Safety Information.

https://www.actemra.com/ra/taking-actemra.html ACTEMRA® (tocilizumab) RA Treatment Options - Learn about ACTEMRA's treatment options for rheumatoid arthritis, subcutaneous injection and intravenous infusion, and what may be best for you. IMPORTANT SAFETY INFORMATION-RA: ACTEMRA is a prescription medicine called an interleukin-6 (IL-6) receptor antagonist. ACTEMRA is used to treat adults with moderately to severely active rheumatoid arthritis (RA) after at least one other medicine called a disease modifying antirheumatic drug (DMARD) has been used and did not work well. 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; if you had hives, a rash, or experienced flushing after injecting, you should tell your doctor or nurse before your next injection); and nervous system problems. Tell your doctor if you're allergic to ACTEMRA or if you've had a reaction to ACTEMRA previously. Common side effects 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. 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. Please see full Prescribing Information, including Medication Guide and Serious Side Effects, for more Important Safety Information.

https://www.actemra.com/ra/taking-actemra/taking-actemra-sc-injections.html ACTEMRA® (tocilizumab) for RA - Subcutaneous Injections - Find step by step instructions for ACTEMRA® (tocilizumab) subcutaneous injections and helpful video and guides here. IMPORTANT SAFETY INFORMATION-RA: ACTEMRA is a prescription medicine called an interleukin-6 (IL-6) receptor antagonist. ACTEMRA is used to treat adults with moderately to severely active rheumatoid arthritis (RA) after at least one other medicine called a disease modifying antirheumatic drug (DMARD) has been used and did not work well. 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; if you had hives, a rash, or experienced flushing after injecting, you should tell your doctor or nurse before your next injection); and nervous system problems. Tell your doctor if you're allergic to ACTEMRA or if you've had a reaction to ACTEMRA previously. Common side effects 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. 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. Please see full Prescribing Information, including Medication Guide and Serious Side Effects, for more Important Safety Information.

https://www.actemra.com/ra/taking-actemra/taking-actemra-iv-infusions.html Taking ACTEMRA® (tocilizumab) for RA - IV Infusions - Find ACTEMRA® (tocilizumab) IV infusion information, the ACTEMRA Medication Guide and tips for your first IV infusion appointment. IMPORTANT SAFETY INFORMATION-RA: ACTEMRA is a prescription medicine called an interleukin-6 (IL-6) receptor antagonist. ACTEMRA is used to treat adults with moderately to severely active rheumatoid arthritis (RA) after at least one other medicine called a disease modifying antirheumatic drug (DMARD) has been used and did not work well. 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; if you had hives, a rash, or experienced flushing after injecting, you should tell your doctor or nurse before your next injection); and nervous system problems. Tell your doctor if you're allergic to ACTEMRA or if you've had a reaction to ACTEMRA previously. Common side effects 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. 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. Please see full Prescribing Information, including Medication Guide and Serious Side Effects, for more Important Safety Information.

https://www.actemra.com/ra/tools-financial-assistance.html Get help paying for your ACTEMRA® (tocilizumab) - Find financial assistance programs for ACTEMRA® RA treatment including the ACT Fast, Co-pay Card, and Genentech Rheumatology Access Solutions Programs. IMPORTANT SAFETY INFORMATION-RA: ACTEMRA is a prescription medicine called an interleukin-6 (IL-6) receptor antagonist. ACTEMRA is used to treat adults with moderately to severely active rheumatoid arthritis (RA) after at least one other medicine called a disease modifying antirheumatic drug (DMARD) has been used and did not work well. 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; if you had hives, a rash, or experienced flushing after injecting, you should tell your doctor or nurse before your next injection); and nervous system problems. Tell your doctor if you're allergic to ACTEMRA or if you've had a reaction to ACTEMRA previously. Common side effects 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. 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. Please see full Prescribing Information, including Medication Guide and Serious Side Effects, for more Important Safety Information.

https://www.actemra.com/ra/tools-financial-assistance/financial-assistance-RA-support-program.html RA and ACTEMRA® Tools and Financial Assistance - Sign up for access to RA support resources including treatment reminders, reimbursement information, free tracking-journal and sharps disposal container. IMPORTANT SAFETY INFORMATION-RA: ACTEMRA is a prescription medicine called an interleukin-6 (IL-6) receptor antagonist. ACTEMRA is used to treat adults with moderately to severely active rheumatoid arthritis (RA) after at least one other medicine called a disease modifying antirheumatic drug (DMARD) has been used and did not work well. 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; if you had hives, a rash, or experienced flushing after injecting, you should tell your doctor or nurse before your next injection); and nervous system problems. Tell your doctor if you're allergic to ACTEMRA or if you've had a reaction to ACTEMRA previously. Common side effects 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. 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. Please see full Prescribing Information, including Medication Guide and Serious Side Effects, for more Important Safety Information.

https://www.actemra.com/ra/tools-financial-assistance/financial-assistance-RA-support-program/join.html Sign up for RA and ACTEMRA® Support - Sign up for total access to ACTEMRA and RA support tools including reimbursement, treatment reminders, and free sharps disposal containers. IMPORTANT SAFETY INFORMATION-RA: ACTEMRA is a prescription medicine called an interleukin-6 (IL-6) receptor antagonist. ACTEMRA is used to treat adults with moderately to severely active rheumatoid arthritis (RA) after at least one other medicine called a disease modifying antirheumatic drug (DMARD) has been used and did not work well. 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; if you had hives, a rash, or experienced flushing after injecting, you should tell your doctor or nurse before your next injection); and nervous system problems. Tell your doctor if you're allergic to ACTEMRA or if you've had a reaction to ACTEMRA previously. Common side effects 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. 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. Please see full Prescribing Information, including Medication Guide and Serious Side Effects, for more Important Safety Information.

https://www.actemra.com/ra/tools-financial-assistance/reminder-program.html ACTEMRA® (tocilizumab) for RA Treatment Reminders - Sign up to receive text messages to remind you of upcoming ACTEMRA® (tocilizumab) injections or infusions. IMPORTANT SAFETY INFORMATION-RA: ACTEMRA is a prescription medicine called an interleukin-6 (IL-6) receptor antagonist. ACTEMRA is used to treat adults with moderately to severely active rheumatoid arthritis (RA) after at least one other medicine called a disease modifying antirheumatic drug (DMARD) has been used and did not work well. 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; if you had hives, a rash, or experienced flushing after injecting, you should tell your doctor or nurse before your next injection); and nervous system problems. Tell your doctor if you're allergic to ACTEMRA or if you've had a reaction to ACTEMRA previously. Common side effects 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. 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. Please see full Prescribing Information, including Medication Guide and Serious Side Effects, for more Important Safety Information.

https://www.actemra.com/ra/tools-financial-assistance/financial-assistance-RA-treatment-support.html RA and ACTEMRA® Treatment Support Tools - Find tools designed to help you manage your ACTEMRA® (tocilizumab) treatments, track your RA symptoms and make the most of your appointments. IMPORTANT SAFETY INFORMATION-RA: ACTEMRA is a prescription medicine called an interleukin-6 (IL-6) receptor antagonist. ACTEMRA is used to treat adults with moderately to severely active rheumatoid arthritis (RA) after at least one other medicine called a disease modifying antirheumatic drug (DMARD) has been used and did not work well. 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; if you had hives, a rash, or experienced flushing after injecting, you should tell your doctor or nurse before your next injection); and nervous system problems. Tell your doctor if you're allergic to ACTEMRA or if you've had a reaction to ACTEMRA previously. Common side effects 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. 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. Please see full Prescribing Information, including Medication Guide and Serious Side Effects, for more Important Safety Information.

https://www.actemra.com/site-map.html Site Map | ACTEMRA® (tocilizumab) - IMPORTANT SAFETY INFORMATION-RA: ACTEMRA is a prescription medicine called an interleukin-6 (IL-6) receptor antagonist. ACTEMRA is used to treat adults with moderately to severely active rheumatoid arthritis (RA) after at least one other medicine called a disease modifying antirheumatic drug (DMARD) has been used and did not work well. 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; if you had hives, a rash, or experienced flushing after injecting, you should tell your doctor or nurse before your next injection); and nervous system problems. Tell your doctor if you're allergic to ACTEMRA or if you've had a reaction to ACTEMRA previously. Common side effects 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. 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. Please see full Prescribing Information, including Medication Guide and Serious Side Effects, for more Important Safety Information.

Country: 52.52.26.231, North America, US

City: -121.8914 California, United States

SPARKY - BEST OF THEM ALL

Have a 1990 toy. celica gt with the org. rear main seal. Put 1 bottle in with a fresh oil change..The car does mainly short trips, and for first 2 weeks really no difference, but then after taking a few highway hour or so trips, it worked by the 3rd week...Rear main seal leak stopped and its been about 2 months now..So I think the key is highway speed trips to really get it to work and heat it up.....I've tried them all, and nothing worked or even came close to AT-205, some even made it worse....Will change the oil next week and use another bottle and see what happens...So far so good....

judy davenport - You just pay for the Rabbit tv usb plugin. If I could leave just no stars, I would. All this is, is a usb unit that you pay to

download on your computer, so they can try to charge you additional fees to see, play or otherwise use and to pay for additional companies wanting to sell you something else like security, clean up computer and etc. Not worth the money. You can already get on the internet for free for what this offers for a fee. don't even thing about getting this, all you do is donate your money. Yes it is cheap, but its not even worth the 10.00. I am glad I purchased it at Wal-Mart, this way I can take it back and get a refund within 30 days. I am just glad I did not order this from tv or off the internet where I would of paid a S & H charge. Boy was I a sucker!!!

DataDoll - Lousy suction and overpriced

I was so excited about this vacuum after seeing the fancy commercials. I read the negative reviews but decided that since I have only two carpeted rooms (others are hardwood and tile) the short battery life wouldn't matter. To my disappointment, the vacuum didn't even clean the two rooms of Berber carpet and the area rugs. It spits fibers right back out and yes, after repeated roll overs trying to pick up what was spit back out, the battery goes dead. What a rip-off, I'm taking it back to Best Buy today for a full refund. Maybe I bought a lemon and I'm tempted to buy another one because it's lightweight and I like the design. I don't know yet, but this one is going back.