Shamburgers/Plandemics: CDC Not Advising to Stop Eating at Wendys after 37 People Get Sick from E-Coli. If Their Food Kills as Many People as COVID Shots (30,000) Will CDC Shut it Down or Mandate it?

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UNLIKE COVID INJECTION PROVIDERS, MANUFACTURERS AND ADMINISTRATORS, WENDY’S CAN BE SUED BY PEOPLE FOR INJURY AND DEATH CAUSED BY CONSUMING ITS UNHEALTHY FOOD.

From [HERE] Wendy’s restaurants have been associated with an E. coli outbreak reported in four states, with 37 people infected and 10 hospitalized, the US Centers for Disease Control and Prevention said Friday. 

No deaths have been reported.

A specific food has not been confirmed as the source of the outbreak, according to the CDC, but 22 of 26 sick people reported eating sandwiches at Wendy’s restaurants in Michigan, Ohio and Pennsylvania before getting sick.

As a precaution, Wendy’s is removing the romaine lettuce being used in sandwiches from restaurants in that region, since most sick people reported eating sandwiches with romaine lettuce, according to the agency.

The CDC said it is not advising that people avoid eating at Wendy’s restaurants or that people stop eating romaine lettuce. 

The agency is investigating to confirm whether romaine lettuce is the source of the outbreak, and whether the lettuce used at the Wendy’s stores was served or sold at other businesses. [MORE]

Meanwhile VAERS data released Friday, August 5, 2022 by the Centers for Disease Control and Prevention show 1,371,474 reports of adverse events from all age groups following COVID-19 vaccines, including 29,981 deaths and 249,116 serious injuries between Dec. 14, 2020, and July 29, 2022.

The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,371,474 reports of adverse events following COVID-19 vaccines were submitted between Dec. 14, 2020, and July 29, 2022, to the Vaccine Adverse Event Reporting System (VAERS). That’s an increase of 13,534 adverse events over the previous week.

VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.

The data included a total of 29,981 reports of deaths — an increase of 191 over the previous week — and 249,116 serious injuries, including deaths, during the same time period — up 1,430 compared with the previous week.

Of the 29,981 reported deaths, 19,348 cases are attributed to Pfizer’s COVID-19 vaccine, 7,981 cases to Moderna, 2,603 cases to Johnson & Johnson (J&J) and no cases yet reported for Novavax.

Excluding “foreign reports” to VAERS, 851,372 adverse events, including 13,894 deaths and 87,050 serious injuries, were reported in the U.S. between Dec. 14, 2020, and July 29, 2022.

Foreign reports are reports foreign subsidiaries send to U.S. vaccine manufacturers. Under U.S. Food and Drug Administration (FDA) regulations, if a manufacturer is notified of a foreign case report that describes an event that is both serious and does not appear on the product’s labeling, the manufacturer is required to submit the report to VAERS.

Of the 13,894 U.S. deaths reported as of July 29, 7% occurred within 24 hours of vaccination, 15% occurred within 48 hours of vaccination and 54% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.

In the U.S., 603 million COVID-19 vaccine doses had been administered as of July 27, including 357 million doses of Pfizer, 227 million doses of Moderna and 19 million doses of Johnson & Johnson (J&J).

Every Friday, VAERS publishes vaccine injury reports received as of a specified date. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed.

Historically, VAERS has been shown to report only 1% of actual vaccine adverse events.

U.S. VAERS data from Dec. 14, 2020, to July 29, 2022, for 6-month-olds to 5-year-olds show:

U.S. VAERS data from Dec. 14, 2020, to July 29, 2022, for 5- to 11-year-olds show:

U.S. VAERS data from Dec. 14, 2020, to July 29, 2022, for 12- to 17-year-olds show:

The most recent report of a death in the 12- to 17-year-old age group was that of a 17-year-old male from Pennsylvania (VAERS I.D. ​2396146) who died from lymphocytic myocarditisapproximately five months after receiving his first dose of Pfizer. The patient had no relevant medical history, according to the report.

The report states the “patient was just hanging with buddies at a soccer game, patient just collapsed, just died right there, EMT rushed patient to hospital and tried 42 minutes of CPR — nothing happened. Once autopsy was done, the patient definitely had myocarditis, and think it was lymphocytic myocarditis.”

The patient did not receive any other vaccine within four weeks of his first dose of Pfizer. The batch and lot number have been requested and “will be submitted if and when received.” However, this information will not be available to the public. 

According to the CDC, “VAERS data available to the public include only the initial report data to VAERS. Updated data which contains data from medical records and corrections reported during follow up are used by the government for analysis. However, for numerous reasons including data consistency, these amended data are not available to the public.”

  • 63 reports of anaphylaxis among 12- to 17-year-olds where the reaction was life-threatening, required treatment or resulted in death — with 97% of cases attributed to Pfizer’s vaccine.

  • 658 reports of myocarditis and pericarditis with 645 cases attributed to Pfizer’s vaccine.

  • 165 reports of blood clotting disorders with all cases attributed to Pfizer.

  • 20 cases of postural orthostatic tachycardia syndrome (POTS) with all cases attributed to Pfizer’s vaccine.

U.S. VAERS data from Dec. 14, 2020, to July 29, 2022, for all age groups combined, show:

Children’s Health Defense (CHD) asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps. [MORE]