TAKEACTION

PLEASE SHARE THIS LINK:
TheCompleteGuideToHealth.com/TakeAction

Please watch the videos below and scroll down the page to learn about a fundamental action that you can take IMMEDIATELY.

The FDA approved the Pfizer injectable bioweapon on Monday, August 23, 2021.

APPROVAL OF THIS BIOWEAPON
IS A CRIMINAL ACT.

The people who approved this bioweapon are guilty of crimes against humanity.

Please take action IMMEDIATELY
to voice your opposition to any such action.

VOICE YOUR OPPOSITION
TO FDA APPROVAL
IN ANY AND ALL WAYS.

BELOW ARE JUST A FEW
THINGS YOU CAN DO.

MAKE PHONE CALLS:

Download the file below that includes the two flyers seen above.

give_these_people_a_piece_of_your_mind_version_2.0.pdf
File Size:	128 kb
File Type:	pdf

Download File

CLICK HERE to scroll all the way down the page for easy access to names, and clickable phone numbers, email addresses and links.

SEND THE EMAIL
TEMPLATE BELOW
TO YOUR
PUBLIC SERVANTS:

Copy the entire email below,
customize it with your
personal signature and use it
to compose an email
to send to all
your public servants.

DEAR PUBLIC SERVANT:

I DEMAND THAT THE FDA IMMEDIATELY REVOKE their approval of the Pfizer COVID-19 "vaccine" until all necessary efficacy and safety studies are completed and substantial evidence demonstrates the benefits of an individual COVID-19 vaccine product outweigh the harms for the indicated, recipient population.

I OPPOSE THE USE OF THESE INJECTABLE BIOWEAPONS WITH EVERY FIBER OF MY BEING.

I DEMAND that YOU review this citizen petition:
https://downloads.regulations.gov/FDA-2021-P-0521-0001/attachment_1.pdf

As of August 13, 2021, OpenVAERS reported:
595,620 adverse events
13,068 deaths
13,812 life threatening events
17,228 permanently disabling injuries
and much more as the result of COVID vaccines being carelessly administered under the Emergency Use Authorization given by the FDA.

Along with the other serious adverse events being reported by OpenVAERS, one would think the FDA, who is supposed to act in the best interest of the public, would be revoking the COVID-19 vaccine EUAs and investigating these serious adverse events instead of moving forward in the approval process for COVID-19 vaccines.

Formal FDA approval will cause more citizens to be murdered by these injectable bioweapons, and cause millions of people to endure more serious and possibly permanent injuries that should be prevented by the FDA. It’s an outrage that the FDA would be so complicit in these crimes against humanity!

As if the numbers listed above aren’t astonishing enough that should serve as a colossal warning to halt the approval of any COVID-19 "vaccines," these numbers come from only 1 of 11 adverse events reporting systems. The VAERS database is the only safety database to which the public has access. The lack of public access to the other 10 reporting systems and the speed at which the COVID-19 "vaccines" are being rushed for approval through the FDA are more than alarming.

The government is withholding extensive safety information from the public despite having at least ten additional data sources and expert consultants to analyze these data, according to Nancy Messonier, MD, the Director of the National Center for Immunization and Respiratory Diseases.

Uniquely for COVID-19, the CDC has developed a parallel system called “V-Safe.” The public cannot access V-Safe data, since it is controlled exclusively by the CDC. VSafe is an app on a smart phone which people can use to report adverse events. I am concerned that the information in V-Safe exceeds that in VAERS which is in defiance of Congress's intent when the created VAERS.

I DEMAND that the FDA consider the information in the current lawsuit filed against XAVIER BECERRA, Secretary of the U.S. Department of Health and Human Services, et al., along with a VAERS whistleblower testimony:
https://img1.wsimg.com/blobby/go/3c6a0774-cfad-46fa-aa97-af5aa5e74f00/M%20for%20PI%20file%20stamped.pdf

I DEMAND that YOU review the following previously submitted petitions AND ACT UPON THEM:
https://www.regulations.gov/document/FDA-2021-P-0460-0001
https://www.regulations.gov/document/FDA-2021-P-0521-0001

I DEMAND that you familiarize yourself with the additional information that can be downloaded here:
https://www.regulations.gov/comment/FDA-2021-P-0521-1070

I DEMAND the the FDA IMMEDIATELY REVOKE the Emergency Use Authorizations for all COVID-19 injectable bioweapons.

I DEMAND that the FDA conduct a thorough investigation to determine the facts behind these absolutely horrific crimes against humanity.

Despite the fact that social media corporations have clearly been conspiring to prevent American citizens from publicly reporting their COVID-19 vaccine related injuries, below you will find an additional list of websites documenting the harm being caused by these injectable bioweapons:

https://www.openvaers.com/covid-data

https://www.thecompleteguidetohealth.com/covid-19-vaccine-injuries.html

https://theempoweror.com/

https://VaxPain.us

https://t.me/s/covidvaccineinjuries

https://1000covidstories.com/

https://www.c19vaxreactions.com/

https://healthimpactnews.com/2021/tens-of-thousands-of-covid-19-vaccine-injured-in-the-u-s-begging-for-help-as-the-medical-community-turns-their-back-on-them/

https://www.facebook.com/profile.php?id=100068922816380

IF YOU IGNORE ALL THE PAIN, SUFFERING AND DEATH THAT THESE INJECTABLE BIOWEAPONS HAVE ALREADY CAUSED, THEN YOU WILL BE HELD PERSONALLY RESPONSIBLE FOR CRIMES AGAINST HUMANITY.

Sincerely,

An American Citizen

CONTACT YOUR
PUBLIC SERVANTS
A.S.A.P.

All of the information below is from publicly provided websites.

These are public servants.

All of their contact information is publicly available.

FDA Consumer Safety Officers:

Jennifer L Bridgewater
240-402-9409
Jennifer.Bridgewater@fda.hhs.gov

Anissa M. Cheung*
*This FDA employee seems to no longer be active.
240-402-9435
Anissa.Cheung@fda.hhs.gov

David W. Dickerson
301-796-1794
David.Dickerson@fda.hhs.gov

Sheila Dreher-Lesnick
240-402-9503
Sheila.Dreher-Lesnick@fda.hhs.gov

Helen S. Gemignani
301-796-0932
Helen.Gemignani@fda.hhs.gov

Christina M. Houck
301-796-2640
Christina.Houck@fda.hhs.gov

Scott E. Norris
240-402-9777
Scott.Norris@fda.hhs.gov

Cassandra K. Overking
240-402-7302
Cassandra.Overking@fda.hhs.gov

Daphne D. Stewart
301-796-2640
Daphne.Stewart@fda.hhs.gov

Leslie D. Wagner
240-402-7456
Leslie.Wagner@fda.hhs.gov

FDA CONSUMER SAFETY OFFICERS
BULK EMAIL LIST (use "bcc"):

Cassandra.Overking@fda.hhs.gov
Christina.Houck@fda.hhs.gov
Daphne.Stewart@fda.hhs.gov
David.Dickerson@fda.hhs.gov
Helen.Gemignani@fda.hhs.gov
Jennifer.Bridgewater@fda.hhs.gov
Leslie.Wagner@fda.hhs.gov
Scott.Norris@fda.hhs.gov
Sheila.Dreher-Lesnick@fda.hhs.gov

Vaccines and Related Biological Products Advisory Committee

Janet Woodcock
Acting FDA Director
301-796-5400
Janet.Woodcock@fda.hhs.gov
Twitter.com/drwoodcockfda

Prabhakara L. Atreya, Ph.D.
ADVISORY COMMITTEE DIRECTOR
240-402-8006
Prabhakara.Atreya@fda.hhs.gov

Kathleen Hayes, M.P.H.
DESIGNATED FEDERAL OFFICER
301-796-7864
Kathleen.Hayes@fda.hhs.gov

Monique Hill, M.H.A.
COMMITTEE MANAGEMENT SPECIALIST
301-796-4620
Monique.Hill@fda.hhs.gov

COMMITTEE MEMBERS:

Hana El Sahly, M.D.
COMMITTEE CHAIRPERSON
713-798-2058
hanae@bcm.edu
FDA.gov/media/98930/download

Moderna's COVID-19 vaccine investigator leaves FDA advisory committee over conflict of interest
https://www.fiercebiotech.com/biotech/moderna-s-covid-vaccine-investigator-leaves-fda-advisory-committee-over-conflict-interest
Top FDA vaccine adviser Hana El Sahly recuses herself over tie to Moderna
https://www.foxnews.com/us/hana-sahly-vaccine-adviser-resign-covid

Paula Annunziato, M.D.***
***Industry Representative (Merck)
1130 Cleaver Rd
Lower Gwynedd, PA 19002
215-643-8225
FDA.gov/media/135870/download

Gregg Sylvester, M.D., M.P.H. +
+Alternate Industry Representative
470 Burnt Mill Road Wilmington, DE 19807
302-272-0653
gcsylvester@gmail.com
FDA.gov/media/135869/download

Archana Chatterjee, M.D., Ph.D.
847-578-3301
Archana.Chatterjee@RosalindFranklin.edu
FDA.gov/media/137429/download

CAPT Amanda Cohn, M.D.
404-639-6039
acohn@cdc.gov
FDA.gov/media/136851/download

Hayley Gans, M.D.
650-723-5682
hagans@stanford.edu
FDA.gov/media/137165/download

Holly Janes, Ph.D.
206-667-6353
hjanes@fredhutch.org
FDA.gov/media/98924/download

Myron Levine, M.D., D.T.P.H., F.A.A.P
410-706-7588
mlevine@som.umaryland.edu
FDA.gov/media/128759/download

H. Cody Meissner, M.D.
617-636-5227
cmeissner@tuftsmedicalcenter.org
FDA.gov/media/117728/download

Paul Offit, M.D.
https://www.paul-offit.com/
215-590-2020
offit@email.chop.edu
paul.offit@gmail.com
FDA.gov/media/117731/download

Steven Pergam, M.D.
206-667-7126
SPergam@fredhutch.org
FDA.gov/media/136854/download

Andrea Shane, M.D., M.P.H., M.Sc.
404-727-9880
ashane@emory.edu
FDA.gov/media/117726/download

Paul Spearman, M.D.
513-636-4578
paul.spearman@emory.edu
FDA.gov/media/117732/download

Geeta K. Swamy, M.D.
919-681-5220
swamy002@mc.duke.edu
FDA.gov/media/117727/download

FDA VACCINE ADVISORY COMMITTEE
BULK EMAIL LIST (use "bcc"):

Archana.Chatterjee@RosalindFranklin.edu
Janet.Woodcock@fda.hhs.gov
Kathleen.Hayes@fda.hhs.gov
Monique.Hill@fda.hhs.gov
Prabhakara.Atreya@fda.hhs.gov
SPergam@fredhutch.org
acohn@cdc.gov
ashane@emory.edu
cmeissner@tuftsmedicalcenter.org
gcsylvester@gmail.com
hagans@stanford.edu
hanae@bcm.edu
hjanes@fredhutch.org
mlevine@som.umaryland.edu
offit@email.chop.edu
paul.offit@gmail.com
paul.spearman@emory.edu
swamy002@mc.duke.edu

ADDITIONAL PUBLIC SERVANTS
TO CONTACT:

Mary A. Malarkey Director
(Named on the Pfizer-BioNTech approval letter)
Office of Compliance and Biologics Quality
Center for Biologics Evaluation and Research
240-402-9008
Mary.Malarkey@fda.hhs.gov
https://www.federalpay.org/employees/food-and-drug-administration/malarkey-mary-anne
https://www.linkedin.com/in/mary-malarkey-a8062998/

Marion Gruber, PhD
(Named on the Pfizer-BioNTech approval letter)
Director
Office of Vaccines Research and Review
Center for Biologics Evaluation and Research
301-796-1856
Marion.Gruber@fda.hhs.gov

Rear Admiral Denise M. Hinton
(Named on the Pfizer-BioNTech Emergency Use Authorization)
The FDA's Chief Scientist
301-796-4880
Denise.Hinton@fda.hhs.gov

Contact all the people here and give them a piece of your mind too:

https://www.fda.gov/about-fda/center-biologics-evaluation-and-research-cber/center-biologics-evaluation-and-research

Individuals becoming aware of any potential violations of the CDC COVID-19 Vaccination Program requirements are encouraged to report them to:

The Office of the Inspector General
U.S. Department of Health and Human Services
800-HHS-TIPS
or https://TIPS.HHS.GOV.