MB Comment: Vaccines cause seizures and the CDC says 10% of kids who have a first seizure end up with epilepsy. This article states that a FDA panel is looking into the issue. Don’t hold your breath. I’ve been to too many sham CDC, FDA and Institute of Medicine meetings to have faith in the integrity of so-called scientists and health authorities to honestly evaluate vaccine adverse reactions. They have too much invested in their on-size-fits-all universal vaccination policy. The pronouncement of panels such as this is typically: We’ve investigated the issue and it’s not the vaccine. It’s never the vaccine for drug company-corrupted scientists. But the FDA Vaccine Adverse Event Reporting System (VAERS) is packed with multiple thousands of reports of rapid-onset seizures and neurological damage after vaccination. If people only knew.
Hopefully, intelligent parents will see through the BS and realize their child is at risk of life-long neurological damage from vaccine adverse reactions, including seizures. When doctors and scientists talk about seizures from vaccines, they are sending a coded message to concerned parents. Open your ears, mothers and fathers. Your child could become another statistic.
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FDA panel recommends pharmacovigilance for certain medications, vaccines
PediatricSuperSite February 2, 2012
The FDA’s Pediatric Advisory Committee met this week and reviewed data relating to several medications currently being used in children, in accordance with the Best Pharmaceuticals for Children Act.
The committee heard data on a number of medications and vaccinations that encompassed a variety of conditions, including attention-deficit/hyperactivity disorder, asthma and human papillomavirus infection …
The panel also recommended continued monitoring of reports on numerous vaccines, including the 13-valent pneumococcal conjugate vaccine (Prevnar13, Wyeth) and bivalent HPV vaccine (HPV2; Cervarix, GlaxoSmithKline). An increased risk for febrile seizure was reported with concomitant administration of the 2010-2011 influenza vaccine (Fluzone, Sanofi-Pasteur) and PCV13 in children aged 6 to 59 months, with the highest risk found in children aged 12 to 23 months. In addition, there were four reports of hypotonic-hyporesponsive episodes that occurred after licensure that the panel agreed warrants further study. As such, the panel recommended further refinement of febrile seizure risk and continued routine pharmacovigilance when administering these vaccines.
The panel also recommended similar measures for Cervarix, after hearing pre- and post-licensure safety data for HPV2. A higher rate of spontaneous abortion was found in a group of women who received HPV2 — 54 women vs. 35 in the control group. Members of the panel said although these “rates do not exceed expected rates” of spontaneous abortion in the general population, they urged further statistical evaluation analysis because cause within the first 90 days of pregnancy could not be excluded.
