Tell the FDA to say NO to Pfizer jabs for babies and toddlers

Update June 12.22 My comment to FDA below

DEADLINE 13 JUNE to comment.

You can help stop this. 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 – 4 years.

Comments received on or before June 7, 2022, will be provided to the committee. However, if you miss that window, you can still comment! The docket will remain open until the meeting, become part of our nation’s public record, and be taken into consideration by the FDA.

Please read to learn more and take action
https://standforhealthfreedom.com/action/no-jabs/

Speak up for the voiceless

DEADLINE 13 JUNE to comment.

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.

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.

FDA accepts comments from citizens of any nation and Health Canada effectively "rubber stamps" whatever the FDA approves. Let your voice be heard.

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.

Please read to learn more and click the green box to submit your comment

https://jamesroguski.substack.com/p/oppose-the-fraud?s=r

Include a link to the Pfizer document

The Food and Drug Administration didn’t 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’s ruling.

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

Pfizer document name [link below]
5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT
REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021

Pages 6 and 7
3 RESULTS
The document reveals that within 90 days after the EUA [emergency use authorization] release of Pfizer’s mRNA vaccine, the company was aware of voluntary adverse reaction reports that revealed 1,223 deaths and over 42,000 adverse reports describing a total of 158,893 adverse reactions.

Page 9
3.1.2 Summary of Safety Concerns in the US Pharmacovigilance Plan
Pfizer knew its vaccine can cause ‘Enhanced Disease’

Page 12
Table 6 Description of Missing Information
The 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).

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 “pending.”

Page 30
Pfizer document includes 9 pages of known adverse events.

https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf

OR

Use this link from UNITY Health & Sciences with key elements highlighted in yellow.

https://unitymovement.ca/wp-content/uploads/2022/05/Pfizer_Cumulative-Analysis-Adverse-Events.pdf

Spread the word

Please, speak up for innocent, voiceless children and share this CALL TO ACTION widely to save their lives. TY!

My comment submitted to FDA

From: no-reply@regulations.gov <no-reply@regulations.gov>
Sent: June-12-22 10:16 PM
To: alignshineprosper@rogers.com
Subject: Your Comment Submitted on Regulations.gov (ID: FDA-2022-N-0904-0001)

Please do not reply to this message.

Your comment was submitted successfully!
Comment Tracking Number: l4c-3t9p-jcfg

Your comment has been sent for review. This process is dependent on agency public submission policies/procedures and processing times. Once the agency has posted your comment, you may view it on Regulations.gov using your Comment Tracking Number.

Agency: FOOD AND DRUG ADMINISTRATION (FDA)
Document Type: Notice
Title: Vaccines and Related Biological Products Advisory Committee; Notice of Meeting; Establishment of a Public Docket; Request for Comments
Document ID: FDA-2022-N-0904-0001

My comment

I urge FDA to say ‘NO’ to expanding Emergency Use Authorization for Pfizer and Moderna’s covid 19 vaccines for children 6 months and over, which are experimental gene therapy injections not vaccines. Tal Zaks, Moderna’s chief medical officer confirmed mRNA injection for covid 19 alters DNA. “We are hacking the software of life.”

Has FDA’s independent committee read the court ordered release of Pfizer’s covid 19 vaccine documents for Adverse Events from the initial rollout 01-Dec-2020 to 28-Feb-2021 with NINE pages of known Adverse Events? https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf

Table 7: Summary shows 158,893 adverse events from 42,086 reported cases, the first 3 months after the vaccines were released to the public. Of those case reports: • 1,223 of the cases list DEATH as the outcome • 9,400 of the cases list UNKNOWN as the outcome (i.e. 22% of the total 42,086 cases) • 11,361 of the cases were NOT RECOVERED at the time of the report (final outcome unknown for these) • Pfizer’s post-authorization data emphasizes that “reports are submitted voluntarily and the magnitude of under-reporting is unknown.”

Man’s natural immunity is robust, children are at low risk, and the injection is known to cause harm.

Maxim of law: He who affirms, not he who denies, must bear the burden of proof.

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