Yesterday, Children’s Health Defense filed a lawsuit against the @US_FDA to obtain documents related to the agency’s safety monitoring of the COVID-19 vaccines through the Vaccine Adverse Events Reporting System (#VAERS) database.
THREAD 🧵
1/10
@US_FDA The lawsuit alleges FDA violated the Freedom of Information Act by refusing to provide key analysis of VAERS reports. The FOIA request was submitted July 2022
@US_FDA .@CDCgov + @US_FDA administer VAERS, a database that allows medical professionals + others to file reports about vaccine-related injuries.
CDC considers VAERS to be an “early warning system” for detecting unusual patterns of reporting that can signal problems w/ a vaccine.
3/10
@US_FDA@CDCgov According to the co-sponsored VAERS’ “Standard Operating Procedures for COVID-19,” dated Jan. 2021 the CDC + FDA would coordinate monitoring for “potential new safety concerns for COVID-19 vaccines” by performing routine VAERS surveillance weekly or bi-weekly, respectively.
4/10
@US_FDA@CDCgov CHD requested these data, along with records of the FDA’s communications with the CDC regarding the CDC’s own COVID-19 vaccine safety monitoring.
The FDA on Oct. 4, 2022, denied CHD’s FOIA request in its entirety.
5/10
@US_FDA@CDCgov The FDA cited “attorney-client privileges” as well as a FOIA exemption that protects agency communications “consisting of opinions, recommendations, and policy discussions within the deliberative process of FDA, from which factual information is not reasonably segregable.”
6/10
@US_FDA@CDCgov CHD’s administrative appeal, filed in Nov. 2022, addressed:
🔴FDA’s failure to explain why it would be impossible to segregate + disclose non-exempt information
🔴What basis it had for claiming attorney-client privilege
🔴Or whether FDA had even searched for the records
7/10
@US_FDA@CDCgov Earlier this month, @EpochTimes obtained the results of CDC’s VAERS analysis, which indicated hundreds of safety signals for the Moderna + Pfizer vaccines, including:
🔴 Blood clotting in the lungs
🔴 Menstrual bleeding
🔴 A lack of oxygen to the heart
🔴 Death
@US_FDA@CDCgov@EpochTimes Thank you for reading. Please QT, RT, share + comment to PUT PRESSURE on our federal agencies to be TRANSPARENT about their vaccine safety data — and DO THEIR JOBS!
“Federal agencies took the unprecedented step of ordering vaccine makers to produce them and recommending them without data supporting their safety or efficacy.”
Moderna's CEO recently claimed, “... we inject mRNA in people’s hearts after a heart attack to grow back new blood vessels and re-vascularize the heart ... It’s a bit like science fiction medicine but that’s what is really exciting to me.”
Let's unpack this.
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On Jan. 9, Moderna told investors it's developing multiple products in its "mRNA pipeline" (yikes) — including a treatment designed to be injected directly into the hearts of patients who have sustained heart failure.
Moderna raked in $18.4 billion for its mRNA vaccine — the company’s only product on the market after a long history of failure, during which safety concerns about the mRNA vax threatened its entire product pipeline according to @_whitneywebb:
COVID-19 vaccine manufacturers, including @Pfizer@moderna_tx and BioNTech, lobbied Twitter and other social media platforms to set moderation rules that would flag purported “misinformation,” according to journalist Lee Fang (@lhfang).
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1/10
The new documents revealed efforts by
✔️ lobbying groups
✔️ nonprofits
✔️ the German government
to influence Twitter to more aggressively limit purported COVID-19 “misinformation.”
RFK, Jr. on Tuesday announced a huge lawsuit with multiple plaintiffs, incl. CHD + Dr. Joseph Mercola, making antitrust + First Amendment claims against mainstream media outlets + Big Tech.
The lawsuit alleges they were censored by Big Tech firms partnering w/ BBC's Trusted News Initiative (TNI), which incl @BBC, The Associated Press (@AP), @Reuters + @washingtonpost
TNI exists to, in its own words, ‘CHOKE OFF’ reporting that it deems ‘misinformation’ 🚩🚩🚩