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Image representing the teeth of a bat with IMOVAX RABIES and IMOGRAM RABIES-HT writen below

Safety Information

  • The most common adverse reactions associated with IMOGAM Rabies–HT Immune Globulin are usually mild and may include tenderness, pain, soreness, and muscle stiffness at the injection site; headache and malaise (a vague feeling of bodily discomfort) may also occur1-3
  • IMOGAM Rabies-HT Immune Globulin is made from human plasma. Because this product is made from human plasma, it may carry a risk of transmitting infectious agents, although prescreening of donors and extensive testing are intended to minimize the risk.
  • IMOGAM Rabies–HT Immune Globulin should NOT be given in repeated doses once post-exposure treatment has been started because it may interfere with the immune response to the rabies vaccine1,2
  • IMOGAM Rabies–HT Immune Globulin should be given with caution to anyone who has had a prior allergic reaction following the administration of human immune globulin2
  • IMOGAM Rabies–HT Immune Globulin contains trace amounts of neomycin; while the risk of allergic reaction is small, it should be given with caution to persons with known hypersensitivities to antibiotics2
  • Although serious adverse reactions to IMOGAM Rabies–HT Immune Globul are very rare, they should be reported to the Vaccine Adverse Event Reporting System (VAERS) via the 24-hour toll-free telephone number (800-822-7967) or on-line at: https://secure.vaers.org/VaersDataEntryintro.htm
  • When administering an intramuscular injection, like IMOGAM Rabies–HT immune globulin, in people with bleeding disorders, caution should be exercised because they may develop a serious bruise or collection of blood at the injection site.

For more information about IMOVAX Rabies vaccine and IMOGAM Rabies–HT Immune Globulin, please talk to your health-care professional.

View full Prescribing Information for IMOGAM Rabies–HT Immune Globulin.

References: 1. Centers for Disease Control and Prevention (CDC). Human rabies prevention—United States, 1999: recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR. 1999;48:1-21. 2. IMOGAM Rabies–HT Prescribing Information, November 2000. 3. Lang J, Gravenstein S, Briggs D, et al. Evaluation of the safety and immunogenicity of a new, heat-treated human rabies immune globulin using a sham, post-exposure prophylaxis of rabies. Biologicals. 1998;26:7-15.

 

 

IMOVAX® Rabies

Indication

IMOVAX Rabies vaccine is indicated for active, pre- and post-exposure immunization against rabies.

 

Safety Information
The most common local and systemic adverse reactions to IMOVAX Rabies vaccine may include injection site pain, erythema, and swelling; headache, nausea, and muscle aches. Other adverse reactions may occur. Once initiated for post-exposure treatment rabies vaccination should not be interrupted or discontinued because of mild local or systemic adverse reactions. Usually such reactions can be successfully managed with anti-inflammatory and antipyretic agents. Vaccination with IMOVAX Rabies vaccine may not protect all individuals.

Before administering IMOVAX Rabies vaccine, please see accompanying full Prescribing Information.

IMOGAM® Rabies–HT

Indication
IMOGAM Rabies-HT immune globulin is given for passive immunization of individuals suspected of exposure to rabies.

Safety Information
Side effects to the IMOGAM Rabies-HT immune globulin include injection site tenderness, pain, and muscle soreness or stiffness. Other side effects may occur. IMOGAM Rabies-HT immune globulin should not be given in repeated doses once vaccine treatment has begun. IMOGAM Rabies-HT immune globulin is made from components of human blood and, therefore, this vaccine may carry a risk of transmitting infectious material, although careful selection of donors and extensive testing are intended to minimize this risk. Treatment with a rabies immune globulin may not protect all individuals.

For more information about IMOGAM Rabies-HT immune globulin, talk to your health-care professional.

Last modified: 5/2/08

 
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This page last updated: 11-Aug-2010