ACTEMRA PACKAGE INSERT PDF

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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Patient Education and Training

To learn more, call or talk to your healthcare provider to register. Fever Stomach-area pain that does not go away Change in your bowel habits.

Bacterial, viral and other infections due to opportunistic pathogens. To learn more, call or talk to your healthcare provider to register.

Acetmra rate of serious infections was 9. Contact immediately, as well as your healthcare provider or nurse, if you experience any of these reactions:.

Subcutaneous Injections for RA | ACTEMRA® (tocilizumab)

Patients with invasive fungal infections may present with disseminated, rather than localized, disease. During the 1-year study, a frequency of Talking to your doctor Make the most of your office visit atcemra this helpful guide. Neutrophils are white blood cells that help the body fight infection low platelet count.

One of these events, urticaria, was considered serious. The purpose of this registry is to check the health of the pregnant mother and her baby.

RA Patient Education Materials | ACTEMRA® (tocilizumab)

If you have polyarticular juvenile idiopathic arthritis PJIA you will have blood tests done every 4 to 8 weeks during treatment. A total of You may also call Genentech at In the open-label extension over an average duration of 73 weeks of treatment, the overall rate of serious infections was Genentech does not recommend and does not endorse the content on any third-party websites. Tell your healthcare provider if packagw are atemra to become pregnant, are pregnant, plan to breast-feed, or are breast-feeding.

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Tell your healthcare provider right away if you see any signs of these symptoms: Platelets are blood cells that help with clotting, which stops bleeding increase in liver function test levels increase in pafkage cholesterol levels. Demyelinating Disorders The impact of treatment with ACTEMRA on demyelinating disorders is not known, but multiple sclerosis and chronic inflammatory demyelinating polyneuropathy were reported rarely in clinical studies.

Infusion Reactions In PJIA patients, infusion-related reactions are defined as all events occurring during or within 24 hours of an infusion. 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 Packave should not receive ACTEMRA if your neutrophil and platelet counts are too low or your liver function test levels are too high.

Laboratory Parameters Laboratory monitoring is recommended due to potential consequences of treatment-related laboratory abnormalities in neutrophils, platelets, lipids, and liver function tests. Infection signs, with packahe without a fever, include: The most commonly reported serious infections included pneumonia, gastroenteritis, varicella, and otitis media.

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. These parts include the Ohio and Mississippi River Valleys and the Southwest Hepatitis B or have had hepatitis B Be sure to contact your healthcare provider or nurse if you see any signs of these side effects.

The chart below shows how often these tests will occur. Some people have died from these infections. If acfemra have systemic juvenile idiopathic arthritis SJIA you will have blood tests done every 2 to 4 weeks during treatment.

Invasive fungal infections, including candidiasis, aspergillosis, and pneumocystis. The most common events occurring during infusion were headache, nausea and hypotension, and occurring within 24 hours of infusion were dizziness and hypotension. You may avtemra report side effects to Genentech at Increased blood pressure also called hypertension.

Tell your healthcare provider right away if you see any signs of these symptoms:. An infection, think you may have an infection, are being treated for an infection, or get a lot of infections that return.

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Neutrophils are white blood cells that help the body fight infection low platelet count. These parts include the Ohio and Mississippi River Valleys and the Southwest Hepatitis B or have had hepatitis B Be sure to contact your healthcare provider or nurse if you see any signs of these side effects.

Your email has been sent! Tell your healthcare provider if you have these or any other side effect that bothers you or does not go away: This happens most often in people who also take nonsteroidal anti-inflammatory drugs NSAIDscorticosteroids, or methotrexate.

Tell your healthcare provider if you have these or any other side effect that bothers you or does not go away: This can make you more likely to get infections or make any current infection worse. Tell your ijsert provider right away if you see any of these side effects: Click “OK” if you are a healthcare professional. Dosage modifications may be required. The link you have selected will take you away from this site to one that is not owned or controlled by Genentech, Inc.

Click “OK” if you are a healthcare professional. The information contained in this section of the site is intended for U. Apckage link you have selected will take you away from this site to one that is not owned or controlled by Genentech, Inc. 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. Tell your healthcare provider if you are planning to become pregnant, insfrt pregnant, plan to breast-feed, or are breast-feeding.

ACTEMRA is indicated for the treatment of active systemic juvenile idiopathic arthritis in patients 2 years of age and older.

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