Our Greater Destiny Blog<\/p>\n
DEADLINE 13 JUNE to comment.<\/strong><\/p>\n You can help stop this.<\/strong> You must tell the USA government what you want for your children. You can make a public comment that will go on record for the FDA to consider as it decides on Emergency Use Authorization for COVID vaccines for children ages 6 months \u2013 4 years.<\/p>\n Comments received on or before June 7, 2022, will be provided to the committee. <\/strong>However, if you miss that window, you can still comment! The docket will remain open until the meeting, become part of our nation\u2019s public record, and be taken into consideration by the FDA.<\/p>\n Please read to learn more and take action DEADLINE 13 JUNE to comment.<\/strong><\/p>\n James Roguski sounded the alarm as FDA considers approving Covid – 19 vaccines for the 6 month – 4 year old age group under their Emergency Use Authorization program.<\/p>\n FDA accepts comments from citizens of any nation and Health Canada effectively “rubber stamps” whatever the FDA approves. Let your voice be heard.<\/p>\n Under the video screen with James Roguski’s image, there is a bright green box which contains a one click link to submit a comment directly to the FDA.<\/p>\n Please read to learn more and click the green box to submit your comment<\/em><\/p>\n https:\/\/jamesroguski.substack.com\/p\/oppose-the-fraud?s=r<\/a><\/p>\n The Food and Drug Administration didn\u2019t get 75 years to release thousands of pages of documents it relied on to license its COVID-19 vaccine. Instead, the federal agency was given eight months to do so per a federal judge\u2019s ruling.<\/p>\n Jan 07.22 Back story https:\/\/www.washingtonexaminer.com\/policy\/healthcare\/judge-scraps-75-year-timeline-for-fda-to-release-pfizer-vaccine-safety-data-giving-agency-eight-months<\/a><\/p>\n Pfizer document name<\/strong> [link below] Pages 6 and 7<\/strong> Page 9<\/strong> Page 12 Among those 34 pregnancies that are known, the report indicates that 28 babies died either in utero or upon birth. Only one outcome was reported as normal, and the remaining five were reported as \u201cpending.\u201d<\/p>\n Page 30<\/strong>
\n<\/em>https:\/\/standforhealthfreedom.com\/action\/no-jabs\/<\/a><\/p>\nSpeak up for the voiceless<\/h2>\n
The FDA has scheduled meetings to consider authorizing the use of Pfizer and Moderna injections in children and infants as young as 6 months. THIS MUST BE STOPPED.<\/h3>\n
Include a link to the Pfizer document<\/h2>\n
\n5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT
\nREPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021<\/p>\n
\n3 RESULTS
\nThe document reveals that within 90 days after the EUA [emergency use authorization] release of Pfizer\u2019s mRNA vaccine, the company was aware of voluntary adverse reaction reports that revealed\u00a01,223<\/strong>\u00a0deaths and over\u00a042,000<\/strong>\u00a0adverse reports describing a total of\u00a0158,893<\/strong>\u00a0adverse reactions.<\/p>\n
\n3.1.2 Summary of Safety Concerns in the US Pharmacovigilance Plan
\nPfizer knew its vaccine can cause \u2018Enhanced Disease\u2019<\/p>\n
\n<\/strong>Table 6 Description of Missing Information
\nThe fact that 88% of the pregnant women injected were not followed throughout their pregnancies is deeply concerning since 124 of the 270 pregnant women had some type of adverse reaction (49 nonserious, 75 serious).<\/p>\n
\nPfizer document includes 9 pages<\/strong> of known adverse events.<\/p>\n