Newly FOIA'd reports reveal the bureaucracy of record keeping & the devastation caused by the COVID-19 vaccines.
The contractor hired to process 1,000 VAERS reports/day overwhelmed by flood of reports in first month of the vaccination campaign.🧵
The contractor is the IT unit of defense industry giant General Dynamics. Hired to process 7,000 reports/week, they were quickly overwhelmed by the the "record setting" number of reports flooding in by January, 2021.
They renegotiated the contract and hired an additional 290 staffers to process a minimum of 25,000 new reports/week plus make their way through almost 95,000 backlogged reports that had piled up by March 1st.
That was 1 of the 7 adverse events recorded for 12-year old clinical trial volunteer Maddie de Garay in the latest #pfizerfiles released under FOIA.
Trial records say it started 1 day after her second dose, but was deemed "unrelated."
Another adverse event recorded on the same day, 'abdominal pain', was deemed "related" to the product.
Both AEs happened on the same day, so why was only one deemed related to the product, while the other -- that was marked serious because it required hospitalization -- wasn't?
More well known is that she was recorded as having "functional abdominal pain" starting on Feb 28. Also not related.
"Functional" just means "we don't know what's causing this."
Except they knew one thing it couldn't be: the experimental vaccine.
Courageous vaccine-injured nurse tells the FDA's advisory committee on vaccines about the 770 safety signals from mRNA COVID jabs that the CDC found and hid from the public.
They don't care, but at least they won't be able to say they didn't know.
FOIA of CDC's VAERS safety signal analysis for mRNA COVID vaccines by @EpochTimes' @ZackStieber shows safety signals for death & a range of thrombo-embolic, cardiac, neurological, haemorrhagic, hematological, immune-system, menstrual & other adverse events in U.S. adults. 🧵
For a full explanation & analysis read my substack post linked below. Continue reading this thread for a summary of key findings.
There were over 750 safety signals, of which over 500 were larger than myocarditis.
CDC found that the number of serious AEs reported in < 2 years for mRNA COVID-19 vaccines was 5.5 x more than all serious reports for vaccines given to adults since 2009 (~73,000 vs. ~13,000).
Want to increase your chances of developing dysautonomia? Get vaccinated!
New study in Nature Cardiovascular Research shows 2.2x increase in risk of dysautonomia diagnosis in 90 days after COVID jab vs. 90 days before. No increase after COVID Dx. 🧵
Symptoms of dysautonomia include: tremors, breathing difficulties, temperature regulation problems, an inability to stay upright, vertigo, fainting, irregular heartbeat, gastrointestinal problems, fatigue and exercise intolerance, brain fog, sensory sensitivity, migraines & more!
While you're at it, you can also increase your chances of being diagnosed with myocarditis, POTS, mast cell disorder, UTI, dizziness, lower back pain, fatigue, edema, hyperlipidemia, anemia, hypertension, anxiety, depression, GERD, cellulitis, eczema & headache. #safeandeffective
New FOIA reveals that as early as August 2020, the CDC was expecting up to 1,000 VAERS reports **per day** for COVID Vaccines "with up to 40% of the reports serious in nature." This represents a 600% increase with 8 times the rate of serious reports. 🧵 jackanapes.substack.com/p/foiad-contra…
In late August 2020, the CDC contracted with General Dynamics to handle VAERS reports for COVID-19 vaccines. The contract anticipated up to 1,000 reports per day, with up to 40% of them serious in nature. The value of the year-long contract was $9.45 million.
This means that months before the EUA of any COVID vaccines, the CDC anticipated up to a 600% increase over the average annual number of VAERS reports in recent years with 8 times the rate of serious reports.