Citizen Petition Urges FDA Against Premature Full Approval of Covid Vaccines

by | Jun 6, 2021 |

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Through several issues of The McCullough Report, US experts have expressed grave concerns over the safety of the mRNA and adenoviral COVID-19 vaccines. These products trick the body into an uncontrolled biologic frenzy and produce the dangerous Wuhan spike protein, which is the product of bioterrorism research from the Institute of Virology in Wuhan, China.

Please see the notice to the US FDA from prominent leaders indicating the products are not sufficiently safe nor effective for full FDA approval. There are several action links below for you to take the initiative.

Citizen Petition Urges FDA Against
Premature Full Approval of Covid Vaccines

Many open, unanswered questions surrounding the efficacy and safety of COVID-19 vaccines must be answered before the FDA considers granting a full approval.

The 20-page Citizen Petition from Linda Wastila and 26 co-authors can be downloaded here and is open for public comment. When FDA responds, it will be public on the regulations.gov docket (Docket ID: FDA-2021-P-0521).

IMPORTANT LINKS:

• Linda Wastila et al. Citizen Petition (Docket ID: FDA-2021-P-0521):
https://downloads.regulations.gov/FDA-2021-P-0521-0001/attachment_1.pdf

• To comment on the Linda Wastila et al. Citizen Petition:
https://www.regulations.gov/commenton/FDA-2021-P-0521-0001

• To read others comments on the Linda Wastila et al. Citizen Petition:
https://www.regulations.gov/document/FDA-2021-P-0521-0001/comment

• Main FDA docket for Linda Wastila et al. Citizen Petition (Docket ID: FDA-2021-P-0521):
https://www.regulations.gov/docket/FDA-2021-P-0521/document

Dr. Peter McCullough

Dr. McCullough is an internist, cardiologist, and epidemiologist managing the cardiovascular complications of both the viral infection and the injuries developing after the COVID-19 vaccine in Dallas, TX, USA.

Since the outset of the pandemic, Dr. McCullough has been a leader in the medical response to the COVID-19 disaster and has published “Pathophysiological Basis and Rationale for Early Outpatient Treatment of SARS-CoV-2 (COVID-19) Infection,” the first synthesis of sequenced multidrug treatment of ambulatory patients infected with SARS-CoV-2 in the American Journal of Medicine and subsequently updated in Reviews in Cardiovascular Medicine. He has 56 peer-reviewed publications on the infection and has extensively commented on the medical response to the COVID-19 crisis in TheHill, America Out Loud, and FOX NEWS Channel.

On November 19, 2020, Dr. McCullough testified in the US Senate Committee on Homeland Security and Governmental Affairs, in 2021-2022, the Texas Senate Committee on Health and Human Services, Colorado General Assembly, New Hampshire Senate, Pennsylvania Senate, and South Carolina Senate concerning many aspects of the pandemic response. On January 24, 2022, Dr. McCullough co-moderated and testified in the US Senate Panel “COVID-19: A Second Opinion” chaired by Senator Ron Johnson. Dr. McCullough has reviewed thousands of reports, participated in scientific congresses, group discussions, and press releases, and has been considered among the world's top experts on COVID-19.

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Scott
Scott
1 year ago

Why was the petiton withdrawn on July 23rd?

Lisa
Lisa
1 year ago

Why was the petition withdrawn on July 23rd?
file:///C:/Users/Lisa/Downloads/FDA-2021-P-0521-1560_attachment_1.pdf
Did you, Dr. McCullough, support this withdrawal? What is being done to curtail the bogus approval by the FDA of these therapeutics (we all know they aren’t vaccines)? What can be done to force FDA to use its standard procedures for all approvals instead of rushing it due to pressure for big pharma and bureaucrats?

Resident
Resident
1 year ago

I’m here because I want to know why the petition was withdrawn too.

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