Latest VAERS Data Show Reports of Blood Clotting Disorders, Summarized by ASL Patriot Broadcast

ROUGH DRAFT!

Latest VAERS Data Show Reports of Blood Clotting Disorders After All Three Emergency Use Authorization Vaccines excerpted from article written by Megan Redshaw, summarized by Lance.

Data released today by the Centers for Disease Control and Prevention (CDC) on the number of injuries and deaths reported to the Vaccine Adverse Event Reporting System (VAERS) following COVID vaccines revealed reports of blood clots and other related blood disorders associated with all three vaccines approved for Emergency Use Authorization in the U.S. — Pfizer, Moderna and Johnson & Johnson (J&J). So far, only the J&J vaccine has been paused because of blood clot concerns. VAERS is the primary mechanism for reporting adverse vaccine reactions in the U.S. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed. Every Friday, VAERS makes public all vaccine injury reports received through a specified date, usually about a week prior to the release date. Today’s data show(gesture to chart) that between Dec. 14, 2020 and April 8, a total of 68,347 total adverse events were reported to VAERS, including 2,602 deaths — an increase of 260 deaths over the previous week — and 8,285 serious injuries, up 314 since last week. Of the 2,602 deaths reported as of April 8, (Top line in chart) 27% occurred within 48 hours of vaccination, 19% occurred within 24 hours and 41% occurred in people who became ill within 48 hours of being vaccinated. In the U.S., 174.9 million COVID vaccine doses had been administered as of April 8. This includes 79.6 million doses of Moderna’s vaccine, 90.3 million doses of Pfizer and 4.9 million doses of the J&J COVID vaccine. This week’s VAERS data show: 19% of deaths were related to cardiac disorders. 55% of those who died were male, 43% were female and the remaining death reports. About 2%, did not include gender of the deceased. As of April 8, 408 pregnant women (gesture to chart) had reported adverse events related to COVID vaccines, including 114 reports of miscarriage or premature birth. Of the 678 cases of Bell’s Palsy reported, (gesture to chart) 59% of cases were reported after Pfizer-BioNTech vaccinations, 38% following vaccination with the Moderna vaccine and 24 cases (4%) of Bell’s Palsy were reported with J&J. There were 77 reports of Guillain-Barré Syndrome with 55% of cases attributed to Pfizer, 40% to Moderna and 10% to J&J. (gesture to chart)
[Lance: Now let me explain what anaphylaxis is: “Anaphylaxis is a severe allergic reaction to venom, food, or medication. Most cases are caused by a bee sting or eating foods that are known to cause allergies, such as peanuts or tree nuts. Anaphylaxis causes a series of symptoms, including a rash, low pulse, and shock, which is known as anaphylactic shock.”] There were 20,021 reports of anaphylaxis with 47% of cases attributed to Pfizer’s vaccine, 46% to Moderna and 7% to J&J. (gesture to chart) Now there are also reports of blood clotting disorders in VAERS. Children’s Health Defense queried the VAERS data(gesture to chart) for a series of adverse events associated with the formation of clotting disorders and other related conditions. VAERS yielded a total of 795 reports for all three vaccines from Dec. 14, 2020, through April 8. Of the 795 cases of clotting reported, there were 400 reports attributed to Pfizer, 337 reports with Moderna and 56 reports with J&J on top of the eight J&J cases under investigation, including the two additional cases added Wednesday. The Defender reported last 16th, although the J&J and AstraZeneca COVID vaccines have been under the microscope for their potential to cause blood clots, mounting evidence suggests the Pfizer and Moderna vaccines also cause clots and related blood disorders. U.S. regulatory officials were alerted to the problem as far back as December 2020. According to the CDC’s website, “the CDC follows up on any report of death to request additional information and learn more about what occurred and to determine whether the death was a result of the vaccine or unrelated.” On March 8, The Defender contacted the CDC with a written list of questions about reported deaths and injuries related to COVID vaccines. We requested information about how the CDC conducts investigations into reported deaths, the status of ongoing investigations reported in the media, if autopsies are being done, the standard for determining whether an injury is causally connected to a vaccine, and education initiatives to encourage and facilitate proper and accurate reporting. It has been 39 days since we first reached out and have yet to receive answers to our questions. The a few more blood clotting stories came just days after federal health officials paused the J&J vaccine. As The Defender reported April 13, the CDC and U.S. Food and Drug Administration (FDA) called for a temporary but immediate halt to the use of J&J’s COVID vaccine while the agencies investigated the vaccine’s possible link to potentially dangerous blood clots. In a joint statement, the agencies said the Advisory Committee on Immunization Practices (ACIP) was reviewing clinical data gathered on six women, one who died, between the ages of 18 and 48 years who developed blood clots after receiving the single-dose J&J vaccine. On April 14, the ACIP held an emergency meeting to vote on whether to lift the pause on J&J’s vaccine or change recommendations for its use. As The Defender reported, the ACIP postponed the vote, extending the pause pending further analysis of data relating to blood clots. The ACIP said it would reconvene for a vote in one week to 10 days. That same day, J&J revealed two more cases of blood clots — one that occurred in a 25-year-old man who suffered a cerebral hemorrhage during a clinical trial and another case of deep-vein-thrombosis in a 59-year-old woman. In its review of J&J’s submission for Emergency Use Authorization in February, the FDA initially urged further surveillance of a slight “numerical imbalance” in blood clotting events after receiving the shot. At the time, it was concluded there was “insufficient” data to determine “a causal relationship” with the vaccine and the J&J  resumed the trial. CDC, multiple states report ‘breakthrough’ COVID cases among fully vaccinated, and breakthrough means that even through this person has been vaccinated, this person still got covid. Houston Health Department said there were 2.46 positive cases out of every 10,000 fully-vaccinated people and it was unclear if those who tested positive contracted the original strand of COVID or a newer variant. Last month, The Defender reported on breakthrough cases in Washington, Florida, South Carolina, Texas, New York, California and Minnesota. On April 6, The Defender reported on 246 breakthrough cases in Michigan, which included three people who died. Children’s Health Defense asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps. https://vaers.hhs.gov/reportevent.html is the link to go to. It’s in the description for you to click on if you need to make any reports. Will people make more and more reports? Time shall tell…

https://childrenshealthdefense.org/defender/vaers-reports-clotting-disorders-all-three-emergency-use-authorization-vaccines/?fbclid=IwAR2bvbGxeXJIiOXLsnd0YFb1Y2MylYGUe90i9ka6F4VKbucLA-pZA-9C4XA
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