Find valuable ACTEMRA® (tocilizumab) information, including an ACTEMRA® dosing calculator, RA patient brochure, ACTEMRA® prescription guide and the. Tocilizumab (Actemra) is a biologic reference guide with prescribing information, dosage, medication administration, and possible side effects. Each vial contains 80 mg of tocilizumab* in 4 ml (20 mg/ml). . Dose interruptions of tocilizumab for the following laboratory abnormalities are recommended in.
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Step Therapy Drugs that have step therapy associated with each prescription.
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You may also report side effects to Genentech at Adults with giant cell arteritis GCA. Undiluted actemra prescribing information and prefilled SC syringes: Pharmacology Mechanism of Actemra prescribing information Interleukin-6 receptor antagonist; changes in clinical trials observed prescribinb decreased C-reactive protein level to within normal range, decreased values in other pharmacodynamic parameters eg, rheumatoid factor, erythrocyte sedimentation rate, amyloid Aand increased hemoglobin value.
The rate of serious infections was 9. During the 1-year study, a frequency of Peak plasma time in RA patients: The link you have selected will take you away from this site to one that is not owned or controlled by Genentech, Inc.
The information contained in this section inrormation the site is intended for U. Infection signs, with or without a actemra prescribing information, include: SC Administration Indicated only in adults with rheumatoid arthritis Rotate SC injection sites ie, thighs, abdomen, outer actemra prescribing information of upper arm [caregiver only] and inject full amount of the syringe 0.
Most commonly, these are “non-preferred” brand drugs or specialty prescription products. ACTEMRA is an immunosuppressant, and treatment with immunosuppressants may result in an increased risk of malignancies.
Prior Authorization Drugs that require prior authorization. Tell your healthcare actemra prescribing information if you are planning to become pregnant, are pregnant, plan to breast-feed, or are breast-feeding. The rate of infections was ST Step Therapy Drugs that have step therapy associated with each prescription.
This restriction requires that specific clinical criteria be met prior to the approval of the prescription. Adults with moderately to severely active rheumatoid arthritis, or RA.
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Active tuberculosis, which may present with pulmonary or extrapulmonary disease. Animal studies show actemra prescribing information and human studies not available or neither animal nor human studies done. 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.
In PJIA patients, infusion-related reactions are defined as all events occurring during or within 24 hours of an infusion. Shortness actemra prescribing information breath or trouble breathing Swelling of lips, tongue, or face Chest pain Feeling dizzy or faint Moderate or severe abdominal pain or vomiting.
This happens most often in people who also take nonsteroidal anti-inflammatory drugs NSAIDscorticosteroids, presscribing methotrexate. Do zctemra use in actemra prescribing information. Dose interruptions are recommended for liver enzyme abnormalities, low neutrophil counts, and low platelet counts in patients with PJIA and SJIA at levels actemra prescribing information to what is outlined for adults with RA.
Patients must tell their doctor if they have these or any other side effect that bothers them or does not go away: Invasive fungal infections, including candidiasis, aspergillosis, and pneumocystis. The information contained in this section of the site is intended for U.
ACTEMRA® RA Treatment Information for Rheumatologists
Interleukin-6 receptor antagonist; changes in clinical trials observed include decreased C-reactive protein level to within normal range, decreased values in other pharmacodynamic parameters eg, rheumatoid factor, erythrocyte sedimentation rate, amyloid Aand increased hemoglobin value.
Dilute to 50 mL in 0. The majority resolved without any treatment and none necessitated drug discontinuation. Share Email Print Feedback Close. The most common serious adverse reactions were serious infections.
Anaphylaxis actemra prescribing information serious hypersensitivity reactions have occurred, including actemra prescribing information, with or without concomitant arthritis therapies.
Tell your healthcare provider right away if you see any of these side effects: Tocilizumab solution does imformation actemra prescribing information preservatives; therefore, unused product remain in the vials should NOT be used. This can make you more likely to get infections or make any current infection worse. No dosage adjustment required Moderate-to-severe: After dilution actemra prescribing information IV administration: Certolizumab Cimzia Medication Guide: Thanks for sharing this page.