WASHINGTON--(BUSINESS WIRE)--During a special meeting of the FDA Vaccines & Related Biological Products Advisory Committee (VRBPAC) held May 7th to discuss new information on contamination of rotavirus vaccines with DNA from two pig viruses, the National Vaccine Information Center (NVIC) called for the FDA to raise legal vaccine safety testing and labeling standards.
“The contamination of rotavirus vaccines with animal virus DNA that was not detected pre or post-licensure is an important wake up call for industry and government,” said NVIC co-founder & president Barbara Loe Fisher. ”Parents being told by federal officials to give their babies Rotarix and RotaTeq vaccine expect those vaccines and others to be free from adventitious agent contamination.”
NVIC called on the FDA to legally require vaccine manufacturers to adhere to binding regulations rather than offering companies non-binding recommendations and to immediately:
NVIC’s Director of Research & Patient Safety, Vicky Debold, PhD, RN, who is also the consumer member of the FDA vaccine advisory committee, urged the FDA to continue to adhere to the precautionary principle and be transparent in its process whenever contaminants are detected in vaccines. “The public has a right to know whatever you learn,” she said.
About Us: NVIC is a non-profit charitable organization advocating for reform of the vaccine safety system since 1982. Dedicated to preventing vaccine injuries and deaths through public education and defending the informed consent ethic in medicine, NVIC does not advise against, or promote use of, vaccines. Over the past three decades, NVIC has represented the vaccine safety concerns of health care consumers on government vaccine advisory and public engagement committees. For more information, visit www.NVIC.org.