Learn about ACTEMRA® treatment for rheumatoid arthritis, giant cell arteritis, systemic juvenile idiopathic arthritis, and polyarticular juvenile idiopathic arthritis. Find instructions for ACTEMRA® (tocilizumab) subcutaneous injections and helpful information on the ACTEMRA® Medication Guide that should help you better. Inside this kit you’ll also find: .. Some patients may be eligible for free drug through the .. Use a quick, dart-like motion to insert the needle all the way into.

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Tell your healthcare provider if you are planning to become pregnant, are pregnant, plan insegt breast-feed, or are breast-feeding. The most common serious adverse reactions were serious infections. Your use of third-party websites is at your own risk and subject to the terms and conditions of use for such sites.

An infection, think you may have an infection, are being treated for an infection, or get a lot of infections that return. Patient Education and Training.

RA, GCA, SJIA, PJIA Treatment | ACTEMRA® (tocilizumab)

Upper respiratory tract infections like common cold and sinus infections. Members have access to online xctemra resources and treatment management tools. Some people actmra died from these infections. Genentech does not recommend and does not endorse the content on any third-party websites. You may also call Genentech at The most common serious infections included pneumonia, urinary tract infection, cellulitis, herpes zoster, gastroenteritis, diverticulitis, sepsis and bacterial arthritis.

Click “OK” if you are a healthcare professional. The chart below shows how often these tests will occur. Your cholesterol levels should be checked 4 to 8 weeks after the start of your treatment, and then every 6 months after that. Your email has been sent!

Actemra® (tocilizumab)

To learn more, call or talk to your healthcare provider to register. In patients who develop an ANC less than per mm 3 treatment is not recommended.

Most common acemra effects Tell your healthcare provider if padkage have these or any other side effect that bothers you or does not go away: Your healthcare provider should do blood tests to check your cholesterol levels 4 to 8 weeks after you start receiving ACTEMRA, and then every 6 months after that You should not receive ACTEMRA if your neutrophil insedt platelet counts are too low or your liver function test levels are too high. This information does not take the place of talking with your healthcare provider about your medical condition or your treatment.

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Shortness of breath or trouble breathing Swelling of lips, tongue, or face Chest pain Feeling dizzy or faint Moderate or severe abdominal pain or vomiting.

These ISRs occurred in a greater proportion of patients at or above 30 kg The link you have selected will take you away from this site to one that is not owned or controlled by Genentech, Inc. Tell your healthcare provider right away packagw you see any signs of these symptoms:.

You should not do both.

Actemra® (tocilizumab)

These elevations did not result in apparent permanent or clinically evident hepatic injury in clinical trials. In the 6-month control period, in SC-I, the frequency of injection-site reactions was Tell your healthcare provider right away if you are experiencing any side effects. Infection signs, with or without a fever, include sweating or chills; shortness of breath; warm, red or painful skin or sores on your body; feeling very tired; muscle aches; blood in phlegm; diarrhea or stomach pain; cough; weight loss; burning when you urinate or urinating more often than normal Any of the following conditions that may give you a higher chance of getting infections.

Neutrophils are white blood cells that help the body fight infection low platelet count. Infection signs, with or without a fever, include: Tell your healthcare provider if you have these or any other side effect that bothers you or does not go away: The information contained in this section of the site is intended for U.

Serious allergic reactions, including death, can happen with ACTEMRA infusions or injections, even if they did not occur with an earlier infusion or injection. The link you have selected will take you away from this site to one that is not owned or controlled by Genentech, Inc. Reviewing the Medication Guide should help you to better understand the risks and benefits of your RA treatment.

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You may also call Genentech at Genentech does not recommend and does not endorse the content on any third-party websites. Infections The rate of infections was If you have polyarticular juvenile idiopathic arthritis PJIA you will have blood tests done every 4 to 8 weeks during treatment. The risks and benefits of treatment with ACTEMRA should be carefully considered prior to initiating therapy in patients with chronic or recurrent infection.

Infection signs, with or without a fever, include sweating or chills; shortness of breath; warm, red or painful skin or sores on your body; feeling very tired; muscle aches; blood in phlegm; diarrhea or stomach pain; cough; weight loss; burning when you urinate or urinating more often than normal Any of the following conditions that may give you a higher chance of getting infections.

The most commonly reported serious infections included pneumonia, gastroenteritis, varicella, and otitis media. To learn more, call or talk to your healthcare provider to register. Patients should be closely monitored for the development of signs and symptoms of infection during and after treatment with ACTEMRA, including the possible development of tuberculosis in patients who tested negative for latent tuberculosis infection prior to initiating therapy. Tell your healthcare provider if you have these or any other side effect that bothers you or does not go away:.

An infection, think you may have an infection, are being treated for an infection, or get a lot of infections that return. If you had hives, a rash, or experienced flushing after injecting, you should tell your healthcare provider or nurse before your next packafe. Once you are ready or your caregiver is ready to inject at home, the video below may help you get started.

One of these events, urticaria, was considered serious. Your healthcare provider may stop your ACTEMRA treatment for a period of time or change your dose of medicine if needed because of changes in these blood test results.

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