Welcome to Issue 5 of the VITAL E-newsletter
December 2008.

This E-newsletter is designed exclusively for clinicians who are teaching patients how to administer Vivaglobin® therapy. It’s your source for what’s happening in the world of Vivaglobin® and its impact on your patient training efforts.

This month, the VITAL™ E-newsletter features:

“The 5 ALIVE Technique”
Here are 5 questions you can easily remember to ask your PI patients regarding their success and satisfaction with their current IVIg therapy. With just 5 questions you can start a dialogue to determine the best therapy option for your patients.

Click here to read on!

To read past issues of the Vital E-newsletter, click on the images below.










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Vol. 1, No. 5, 2008

Training Tip

Now that you’ve been reading the VITAL E-newsletter for 5 issues, take the “Vivaglobin® Self-Assessment Quiz” to test your knowledge of how to self-administer Vivaglobin® at home.

Take the Quiz here!

Share your Vivaglobin® tips and case studies with us

If you have a Vivaglobin® tip or case study of interest, please submit it to VITAL™ by clicking here

> Contact Us

 


The VITAL E-newsletter is exclusively for infusion nurses and other healthcare professionals like you. It’s your source for what’s happening in the world of Vivaglobin® and how those events can impact on your interactions with patients. Be sure to look for bimonthly issues of the VITAL E-newsletter for updates and complete coverage of current and relevant topics.

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Important Safety Information:
Immune Globulin Subcutaneous (Human), Vivaglobin®, is indicated for the treatment of patients with primary immunodeficiency (PI).

As with all immune globulin products, Vivaglobin® is contraindicated in individuals with a history of anaphylactic or severe systemic response to immune globulin preparations and in persons with selective immunoglobulin A deficiency who have known antibody against IgA. If anaphylactic or anaphylactoid reactions are suspected, discontinue administration immediately and treat as medically appropriate.

Vivaglobin® is derived from human plasma. As with all plasma-derived products, the risk of transmission of infectious agents, including viruses and, theoretically, the Creutzfeldt-Jakob disease (CJD) agent, cannot be completely eliminated.

In clinical trials, the most frequent adverse event was injection-site reaction, consisting of mild or moderate swelling, redness, and itching. No serious local site reactions were observed, and reactions tended to decrease substantially after repeated use. Other adverse events irrespective of causality included headache, gastrointestinal disorder, fever, nausea, sore throat, and rash.

As with all immune globulin (Ig) products, patients receiving Ig therapy for the first time, receiving a new product, or not having received Ig therapy within the preceding eight weeks may be at risk for developing reactions including fever, chills, nausea, and vomiting. On rare occasions, these reactions may lead to shock. Such patients should be monitored in a clinical setting during the initial administration.

Ig administration can transiently impair the efficacy of live attenuated virus vaccines, such as measles, mumps and rubella. In clinical studies, administration of Vivaglobin® has been shown to be safe and well tolerated in both adult and pediatric subjects. No pediatric-specific dose requirements were necessary to achieve the desired serum IgG levels. Safety and efficacy were not studied in pediatric subjects under two years of age.

Please see full prescribing information.

CSL Behring
1020 First Avenue
PO Box 61501
King of Prussia, PA 19406-0901