Rhodesian Ridgebacks could be dying due to over-vaccinations

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The serological studies of Dr. Ronald Schultz of the University of Wisconsin School of Veterinary Medicine showed that dogs had antibody titers counts at levels known to confer immunity to rabies 7 years after vaccination, the results of which have been incorporated into the 2003, 2006 American Animal Hospital Association’s Canine Vaccine Guidelines as well as WSAVA’s 2007 Vaccine Guidelines.

Because the rabies vaccine is the most potent of the veterinary vaccines and associated with significant adverse reactions, it should not be given more often than is necessary to maintain immunity.  Adverse reactions such as autoimmune diseases affecting the thyroid, joints, blood, eyes, skin, kidney, liver, bowel and central nervous system; anaphylactic shock; aggression; seizures; epilepsy; and fibrosarcomas at injection sites are linked to rabies vaccinations.

Rabies is a “killed” vaccine and contains adjuvants to enhance the immunological response.  Mercury (Thimersol) is commonly found as a preservative in killed, adjuvanted veterinary vaccines such as Rabies, Leptospira, and Lyme.  The combination of mercury with adjuvant components (aluminum hydroxide, aluminum phosphate) are of considerable concern because of the reactive properties of aluminum, when in contact with mercury.  Reactivity with aluminum is so acute that mercury may not be packed in checked or carry-on baggage on commercial airplanes, and there is currently a petition to Congress Petition to Congress, Removal of Aluminum Additive in Vaccines Resolution and Petition, citing as cause for removing aluminum in human vaccines that:  "The combination of mercury plus aluminum is far worse than the sum of the two toxicities added together.  The synergistic toxicity could be increased to unknown levels."  

In 1999, the World Health Organization " classified veterinary vaccine adjuvants as Class III/IV carcinogens with Class IV being the highest risk," and the results of a study published in the August 2003 Journal of Veterinary Medicine documenting fibrosarcomas at the presumed injection sites of rabies vaccines stated, “In both dogs and cats, the development of necrotizing panniculitis at sites of rabies vaccine administration was first observed by Hendrick & Dunagan (1992).”  According to the 2003 American Animal Hospital Association’s Canine Vaccine Guidelines, "...killed vaccines are much more likely to cause hypersensitivity reactions (e.g., immune-mediated disease)."

A clarification on the Postmarketing Surveillance of Rabies Vaccines for Dogs to Evaluate Safety and Efficacy referenced in the story.  Only the 246 adverse reactions to the rabies vaccine reported directly to the Center for Veterinary Biologics by the public, veterinarians, and pet owners had 72% of the dogs receiving other vaccines or drugs at the same time as the rabies shot. That is not stated to be the case further on in the report where they discuss the 10,000 adverse reactions reported by the rabies vaccine manufacturers, 65% of which were in dogs.   

If the 6,500 of canine adverse rabies vaccine reactions reported by the vaccine manufacturers represents "only about 1% of serious events are reported to the FDA,” then that would translate into 650,000 if all reactions were reported.

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