The CDC’s own research has found that the long denied vaccine-SIDS link is real.

If you believe the official pronouncements of top governmental health agencies like the CDC and FDA, all the vaccines in the present day schedule are a priori safe and effective.

Not only are you told that they can’t harm you, but that not taking them can kill you.

Parents are under even more pressure. They are told that refraining from vaccinating their infants or children will greatly increase their risk of dying or being disabled. Worse, they are increasingly labeled as ‘crazy’ and ‘irresponsible’ anti-vaccine zealots who are putting the lives of others in danger.

But what happens when the actual evidence from the scientific and clinical literature produced by these very agencies contradicts their own vaccine policies?

This is exactly what has happened with the publication of a new study in the Journal of Pediatrics titled ,”Adverse Events following Haemophilus influenzae Type b Vaccines in the Vaccine Adverse Event ReportingSystem, 1990-2013,” wherein CDC and FDA researchers identify 749 deaths linked to the administration of the Hib vaccine, 51% of which were sudden infant death linked to the administration of Hib vaccine.

The CDC has boldly denied that there is any evidence supporting a causal link between vaccines and infant death, despite the fact that their own webpage on the topic acknowledges that “From 2 to 4 months old, babies begin their primary course of vaccinations. This is also the peak age for sudden infant death syndrome (SIDS).” Written off as coincidence, the CDC suggests that stomach sleeping is the primary modifiable risk factor.

Because SIDS is the 3rd leading cause of death in infants, and because the U.S. has one of the highest infant mortality rates in the developed world, one would think that more progress would have been made toward understanding its causes. Perhaps, as explored in this past article, the signal of harm is being ignored. Neglect and suppression of available data has recently been exposed with the confession of a top CDC vaccine scientist who was compelled to covered up data revealing an autism-MMR link in African-American boys.

In the new study, the CDC and FDA researchers themselves acknowledge “the scarcity” of postlicensure safety data on HiB vaccines in today’s vaccination schedule. They evaluated reports involving the currently licensed Hib vaccines received from January 1, 1990, through December 1, 2013 available on the Vaccine Adverse Event Reporting System (VAERS).

Presently, the CDC recommends 4 doses of the HiB vaccine at the following ages: 2 months, 4 months, 6 months, 12 months through 15 months.

The HiB vaccine is described on the CDC website as “very safe” and “effective” at preventing HiB disease, which it states can be deadly. They list “most common side effects as usually mild and last 2 or 3 days,” including “redness, swelling, and warmth where the child got the shot” and “fever”. Nowhere is there listed death or disability as a possible side effect.

In stark contrast to these statements the study uncovered the following highly concerning results:

J Pediatr. 2015 Jan 15. pii: S0022-3476(14)01163-9. doi: 10.1016/j.jpeds.2014.12.014. [fusion_builder_container hundred_percent=”yes” overflow=”visible”][fusion_builder_row][fusion_builder_column type=”1_1″ background_position=”left top” background_color=”” border_size=”” border_color=”” border_style=”solid” spacing=”yes” background_image=”” background_repeat=”no-repeat” padding=”” margin_top=”0px” margin_bottom=”0px” class=”” id=”” animation_type=”” animation_speed=”0.3″ animation_direction=”left” hide_on_mobile=”no” center_content=”no” min_height=”none”][Epub ahead of print]

Adverse Events following Haemophilus influenzae Type b Vaccines in the Vaccine Adverse Event Reporting System, 1990-2013.

Abstract

OBJECTIVE:

To characterize adverse events (AEs) after Haemophilus influenzae type b (Hib) vaccines reported to the US Vaccine Adverse Event Reporting System (VAERS), a spontaneous reporting surveillance system.

STUDY DESIGN:

We searched VAERS for US reports after Hib vaccines among reports received from January 1, 1990, to December 1, 2013. We reviewed a random sample of reports and accompanying medical records for reports classified as serious. All reports of death were reviewed. Physicians assigned a primary clinical category to each reviewed report. We used empirical Bayesian data mining to identify AEs that were disproportionally reported after Hib vaccines.

RESULTS:

VAERS received 29 747 reports after Hib vaccines; 5179 (17%) were serious, including 896 reports of deaths. Median age was 6 months (range 0-1022 months). Sudden infant death syndrome was the stated cause of death in 384 (51%) of 749 death reports with autopsy/death certificate records. The most common nondeath serious AE categories were neurologic (80; 37%), other noninfectious (46; 22%) (comprising mainly constitutional signs and symptoms); and gastrointestinal (39; 18%) conditions. No new safety concerns were identified after clinical review of reports of AEs that exceeded the data mining statistical threshold.

CONCLUSION:

Review of VAERS reports did not identify any new or unexpected safety concerns for Hib vaccines.

Copyright © 2015 Elsevier Inc. All rights reserved.

 

http://www.ncbi.nlm.nih.gov/pubmed/25598306[/fusion_builder_column][/fusion_builder_row][/fusion_builder_container]