https://www.thegatewaypundit.com/2022/12/gateway-pundit-reported-year-fda-finally-admits-pfizer-covid-vaccine-causes-blood-clots/
As The Gateway Pundit Reported for Over a Year – FDA Finally Admits Pfizer Covid Vaccine Causes Blood Clots
During a COVID-19 EU hearing
last October, Pfizer’s President of International Developed Markets,
Janine Small, admitted that the vaccine had never been tested on its
ability to prevent transmission, contrary to what was previously
advertised.
During the hearing, when asked by Dutch politician Ross if the Pfizer
COVID vaccine tested on stopping the transmission of the virus before
it entered the market, Janine Small responded while smiling,
“Regarding the question around did we know about stopping
immunization before it entered the market? No. We have to really move at
the speed of science to really understand what is taking place in the
market.”
This statement was confirmed by an unredacted Pfizer agreement from a FOIA request with the Slovenian government.
Here is a little snippet that indicates that Pfizer is evolving each
component of the “vaccine”, presumably advising all deviations from
clinical trial dosages and regimens to each EU member state (and every
other country that has taken Pfizer injections).
“The Participating Member State acknowledges that the Vaccine and
materials related to the Vaccine, and their components and constituent
materials are being rapidly developed due to the emergency circumstances
of the COVID-19 pandemic and will continue to be studied after
provision of the Vaccine to the Participating Member States under the
APA,” according to the documents.
“The Participating Member State further acknowledges that the
long-term effects and efficacy of the Vaccine are not currently known
and that there may be adverse effects from the Vaccine that are not
currently known.”
Pfizer clearly states in the supply contract that the injections are not
going to be the same as the clinical trial injections AND it has no
clue as to long-term effects or efficacy AND there may be unknown
adverse effects that are, presumably, ABOVE and BEYOND the adverse event
rate of 24% in the injected group of 21,900 in the Pfizer phase 3
clinical trials v 6% in the 21,900 placebo group in those trials!
In November, The Gateway Pundit reported that big pharmaceutical companies Pfizer and Moderna have both begun clinical tests
to investigate whether or not the use of their experimental COVID
vaccines may have any long-term adverse effects on a person’s health.
Reports from the Vaccine Adverse Events Reporting System (VAERS)
including non-domestic reports showed there are now over 1.4 million
cases of COVID-19 vaccine adverse reactions including more than 32,828
deaths through December 9, 2022.
After two years, FDA finally admitted Pfizer’s COVID-19 vaccine had been linked to blood clotting in older individuals based on the result of one of the largest studies of elderly persons aged 65 years and above.
Epoch Times reported:
Researchers looked at data covering 17.4 million elderly Americans
who received a total of 34.6 million vaccine doses between Dec. 10,
2020, and Jan. 16, 2022.
The study was published by the journal Vaccine on Dec. 1.
FDA researchers, with assistance from researchers with the Centers
for Medicare & Medicaid Services (CMS), analyzed data from the CMS
database. They included Medicare Fee-for-Service beneficiaries aged 65
or older who received a vaccine within the timeframe, were enrolled when
they were vaccinated, and were enrolled for a “clean window” of time
prior to vaccination. The window was 183 days or 365 days, depending on
the outcome.
About 25 million people receive the Medicare Fee-for-Service, but
only about 17 million were vaccinated during the period of time studied.
Researchers used probability testing to detect an increased risk of
one or more of 14 outcomes following vaccination. The goal was to see
whether vaccination may increase the risk of adverse outcomes, such as
pulmonary embolism, or blood clotting in the lungs. If an outcome met a
certain statistical threshold, that meant it could increase the risk.
All three vaccines have been linked to a number of side effects.
Heart inflammation is causally linked to the Moderna and Pfizer shots,
experts around the world have confirmed, while Johnson & Johnson’s
has been associated with blood clots.
Other conditions, such as pulmonary embolism, have been reported to authorities and described in studies, though some papers have found no increase in risk following vaccination.
Approximately 4,214 reports of post-vaccination pulmonary embolism,
including 1,886 reports following receipt of Pfizer’s vaccine, have been
reported to the U.S. Vaccine Adverse Event Reporting System as of Dec.
9.
As of the same date, 1,434 reports of post-vaccination myocardial
infarction, including 736 following receipt of Pfizer’s vaccine; 469
reports of post-vaccination immune thrombocytopenia, including 234
following receipt of Pfizer’s vaccine; and 78 reports of
post-vaccination intravascular coagulation, including 42 after receipt
of Pfizer’s vaccine, have been reported.
Reports to the system can be made by anybody, but most are lodged by
health care workers, studies show. The number of reports are an
undercount, according to studies.
The new study states that the FDA “strongly believes the potential
benefits of COVID-19 vaccination outweigh the potential risks of
COVID-19 infection.” No evidence was cited in support of the belief.
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