ACTEMRA PRESCRIBING INFORMATION DOWNLOAD
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.
|Published (Last):||27 December 2017|
|PDF File Size:||14.87 Mb|
|ePub File Size:||3.23 Mb|
|Price:||Free* [*Free Regsitration Required]|
Thanks for sharing this page. There was no clear relationship between decreases in neutrophils below 1 x 10 9 per L and the occurrence of serious infections. 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.
Administer first SC dose instead of the next scheduled IV dose. Increased blood pressure also called hypertension. One of these events, urticaria, was considered serious. Fully diluted tocilizumab solutions actemra prescribing information compatible with polypropylene, polyethylene and polyvinyl chloride infusion bags actemra prescribing information polypropylene, polyethylene and glass infusion bottles.
Adults with moderately to severely active actemra prescribing information arthritis, or RA. The rate of serious infections was 9.
The presxribing contained in this section of the site is intended for U. No dosage adjustment required Moderate-to-severe: Forms and Actemra prescribing information Here you can download the form you need to enroll in Genentech Rheumatology Access Solutions and other important information.
Actemra (tocilizumab) dosing, indications, interactions, adverse effects, and more.
Bacterial, viral and other infections due actemra prescribing information opportunistic pathogens. The fully diluted tocilizumab solutions for infusions should be stored at 36 — 46 degrees Fahrenheit or at room temperature for up to 24 hours.
People with active polyarticular juvenile idiopathic arthritis PJIA age 2 years and above. Our patient support prescrribing is designed to help you better manage life actwmra rheumatoid arthritis. Infections The rate of infections was Your doctor also has actemra prescribing information fill out a form called the SMN. Create Your List of Plans.
Patients must tell their doctor if they are planning to become pregnant, are pregnant, plan to breast-feed, or are breast-feeding. Recommended overview Procedures.
FDA Internet Application Site (Accessdata) Error
Tell your healthcare provider if you are planning to become pregnant, are pregnant, plan to breast-feed, or are breast-feeding. Your healthcare provider should do blood tests to check your cholesterol levels 4 to 8 weeks after you actemra prescribing information receiving ACTEMRA, and then every 6 months after that You should not receive Actemra prescribing information if your neutrophil and platelet counts are too low or your liver function test levels are too high.
In PJIA patients, infusion-related reactions are actemra prescribing information as all events occurring during or within 24 hours of an infusion. Neutrophils are white blood cells that help the body fight infection low platelet count. Thanks for sharing this page. Your email has been sent!
Prescribers should exercise caution in considering the use of ACTEMRA in patients with preexisting or recent-onset demyelinating disorders.
To learn more, call or talk to your healthcare provider to innformation. Anaphylaxis or serious hypersensitivity reactions actemra prescribing information occurred, including fatalities, with or without concomitant arthritis therapies. The rate of infections was Pregnancy exposure registry that monitors pregnancy outcomes in women exposed to during pregnancy; patients and pregnant women are encouraged to register themselves by calling SC Administration Indicated only in adults with rheumatoid arthritis Rotate SC injection sites ie, thighs, abdomen, outer area of upper arm [caregiver only] and inject full amount of the syringe 0.
Here you can download the form you prescirbing to enroll in Genentech Actemra prescribing information Access Solutions and other important information. Tell your healthcare provider right away if you prsecribing experiencing any side effects.
Please select a treatment to continue
Peak plasma time in GCA patients: You may also report side effects to Genentech at Two additional patients actemra prescribing information MAS during the long-term extension. Tier Description 1 This drug is available at the lowest co-pay.
Do not use in pregnancy. Serious allergic reactions Serious allergic reactions, including death, can happen with ACTEMRA infusions or injections, actemra prescribing information if they did not informayion with an earlier infusion or injection. Your cholesterol levels should be checked 4 to 8 weeks after the start of your treatment, and then every 6 months after that.
Actemra prescribing information Interactions Sort By: