Shes Acknowledging Theres Surveillance. Again

Authored by Megan Redshaw via ChildrensHealthDefense.org,

Data released today by the Centers for Disease Control and Prevention (CDC) on the number of injuries and deaths reported to the Vaccine Agin Issue Reporting Organization (VAERS) following COVID vaccinesrevealed reports of claret clots and other related claret disorders associated with all three vaccines approved for Emergency Use Authorization in the U.S. — Pfizer, Moderna and Johnson & Johnson (J&J). And then far, just the J&J vaccine has been paused because of claret clot concerns.

VAERS is the master mechanism for reporting agin vaccine reactions in the U.S. Reports submitted to VAERS crave further investigation before a causal relationship can be confirmed.

Every Friday, VAERS makes public all vaccine injury reports received through a specified appointment, unremarkably nigh a week prior to the release date. Today's information bear witness that between Dec. xiv, 2020 and April 8, a total of 68,347 total adverse events were reported to VAERS, including 2,602 deaths — an increase of 260 over the previous week — and 8,285 serious injuries, up 314 since last week.

Of the 2,602 deaths reported as of April eight, 27% occurred within 48 hours of vaccination, 19% occurred inside 24 hours and 41% occurred in people who became ill within 48 hours of existence vaccinated.

In the U.S., 174.9 1000000 COVID vaccine doses had been administered as of April 8. This includes 79.half-dozen meg doses of Moderna'southward vaccine, 90.three meg doses of Pfizer and 4.9 1000000 doses of the J&J COVID vaccine.

This calendar week's VAERS data show:

  • 19% of deaths were related to cardiac disorders.

  • 55% of those who died were male person, 43% were female and the remaining death reports did non include gender of the deceased.

  • Theboilerplate historic period of those who died was 77 and the youngest expiry was an xviii-year-sometime. There are a few reported deaths in children under 18, but these reports contained errors.

  • As of Apr 8, 408 significant women had reported adverse events related to COVID vaccines, including 114 reports of miscarriage or premature nascency.

  • Of the678 cases of Bong'south Palsy reported, 59% of cases were reported subsequently Pfizer-BioNTech vaccinations, 38% following vaccination with the Moderna vaccine and 24 cases (four%) of Bong'southward Palsy were reported with J&J.

  • At that place were 77 reports of Guillain-BarrĂ© Syndrome with 55% of cases attributed to Pfizer, twoscore% to Moderna and x% to J&J.

  • There were20,021 reports of anaphylaxiswith 47% of cases attributed to Pfizer's vaccine, 46% to Moderna and 7% to J&J.

Reports of blood clotting disorders in VAERS

Children'due south Health Defense force queried the VAERS data for a series of adverse events associated with the formation of clotting disorders and other related atmospheric condition. VAERS yielded a full of 795 reports for all three vaccines from Dec. fourteen, 2020, through Apr 8.

Of the 795 cases reported, there were 400 reports attributed to Pfizer, 337 reports with Moderna and 56 reports with J&J — far more than than the 8 J&J cases under investigation, including the two additional cases added Midweek.

As The Defender reported today, although the J&J and AstraZeneca COVID vaccines accept been under the microscope for their potential to cause blood clots, mounting evidence suggests the Pfizer and Moderna vaccines also cause clots and related claret disorders. U.South. regulatory officials were alerted to the problem as far back every bit December 2020.

CDC ignores The Defender, no response later on 39 days

According to the CDC's website, "the CDC follows upwardly on whatever report of decease to request boosted information and acquire more than nearly what occurred and to determine whether the death was a upshot of the vaccine or unrelated."

On March 8, The Defender contacted the CDC with a written listing of questions about reported deaths and injuries related to COVID vaccines. Nosotros requested data virtually how the CDC conducts investigations into reported deaths, the condition 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 pedagogy initiatives to encourage and facilitate proper and accurate reporting.

Later on many attempts to get a response from the CDC, 22 days after our initial outreach a representative from the CDC's Vaccine Task Forcefulness responded, saying the bureau had never received our questions — fifty-fifty though the employees we talked to several times said their press officers were working through the questions we sent.

We provided the questions again and fix a new borderline of Apr vii. We've reached out multiple times since, but the representative has not answered our emails or returned our calls.

On April fifteen we chosen the CDC's general media line again and were told they had our list of questions and were unsure why the representative told us she never received them. Nosotros were told the COVID response team would be informed and that we should follow up in a few days.

It has been 39 days since we first reached out and accept yet to receive answers to our questions.

Johnson & Johnson paused over reports of blood jell

On April 15, The Defender reported that a healthy 43-year quondam human in Mississippi suffered a stroke hours after being vaccinated with J&J'south COVID vaccine. Brad Malagarie, father of vii, had received the vaccine a little after Noon and was institute unresponsive by co-workers at his desk.

Also on Apr xv, the  Cincinnati Enquirer reported that the Ohio Department of Wellness is monitoring the investigation into what may have caused a 21-twelvemonth-old University of Cincinnati student to die all of a sudden last Sunday, about a day after he received the J&J vaccine.

Alicia Shoults, a spokeswoman for the country health section, said the agency is waiting for the completion of a Hamilton County coroner's report, and "if necessary," further guidance from the CDC.

The two news stories came just days subsequently 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 simply firsthand 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 argument, the agencies said the Informational Commission on Immunization Practices (ACIP) was reviewing clinical data gathered on six women, one who died, betwixt the ages of 18 and 48 years who developed blood clots afterwards receiving the single-dose J&J vaccine.

On Apr 14, the ACIP held an emergency coming together to vote on whether to elevator the pause on J&J's vaccine or change recommendations for its utilise. 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 ane calendar week to 10 days.

That same day, J&J revealed two more cases of claret clots — one that occurred in a 25-year-old human who suffered a cognitive 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 Authority in February, the FDA initially urged further surveillance of a slight "numerical imbalance" in blood clotting events afterwards receiving the shot. At the time, it was ended at that place was "insufficient" data to determine "a causal relationship" with the vaccine and the drugmaker resumed the trial.

As The Defender reported April 12, the rollout of J&J's COVID vaccine has non been smooth. At the commencement of the month the vaccine maker had to throw out 15 million doses of its vaccine after they were contaminated with AstraZeneca vaccine ingredients at an unapproved manufacturing institute in Baltimore.

The vaccine maker likewise has been plagued with shutdowns of its vaccine sites prior to the vaccine beingness paused, multiple reports of COVID breakthrough cases and criticism over its CEO's $30 1000000 pay packet while the visitor pays out billions for its part in the opioid epidemic.

CDC, multiple states written report 'breakthrough' COVID cases among fully vaccinated

Cases of fully vaccinated people getting COVID, referred to as "quantum" cases, proceed to make news.

Calling it a "actually good scenario," the CDC yesterday reported five,800 cases of COVID in fully vaccinated people. Of the five,800 cases, 396 required hospitalization and 74 people died, the CDC said.

The CDC said it was "keeping a close eye" on the cases, simply that breakthrough cases are to be expected. Tara Smith, a professor of epidemiology at the Kent State University College of Public Health in Ohio, told NBC News:

"This is a really good scenario, fifty-fifty with almost vi,000 breakthrough infections. Most of those have been mildly symptomatic or asymptomatic. That'southward exactly what we were hoping for."

On April 12, the Houston Health Department reported 142 quantum cases of COVID that occurred in fully vaccinated people since Jan, according to ABC 13 News. Vaccine recipients received either two doses of Moderna or Pfizer, or one dose of J&J. The report ruled out those who were said to have contracted the virus 45 days before their second scheduled shot appointment.

Houston Health Department said there were ii.46 positive cases out of every 10,000 fully-vaccinated people and information technology 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 agin reaction, to any vaccine, to file a report following these 3 steps.

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Source: https://www.zerohedge.com/covid-19/what-cdcs-vaers-database-reveals-about-adverse-post-vaccine-reactions

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