Case Report: Pfizer COVID Vaccine ‘Catalyst’ in Death of 34-Year-Old Man

When Henrietta Simoes’ son Victor died suddenly 16 days after his first dose of the…

Children's Health Defense

When Henrietta Simoes’ healthy, flourishing 34-year-old son Victor died suddenly on May 6, 2021, 16 days after his first dose of the Pfizer COVID-19 vaccine, she began seeking answers.

More than three years later, on Aug. 8, Biomedical Science and Clinical Research published a peer-reviewed case report, detailing the mechanisms through which the vaccine caused an acute aortic dissection that killed her son.

The report was based on the analyses of Victor’s data that she and her family obtained from researchers across the world.

Henrietta hopes the study will be an important tool in the struggle to bring those responsible for the damage caused by the COVID-19 vaccines to justice.

“I can’t get my son back, so it’s not going to help me in that sense,” Henrietta told The Defender. “But I don’t want this to happen to anybody else, ever again. We need to get justice and we can’t ever let it go.”

Henrietta hopes there will someday be criminal prosecutions for the pharmaceutical industry executives, public health officials and politicians who pushed through the vaccine emergency use authorizations, recommendations and mandates.

The study provides a detailed analysis of Victor’s case using evidence from his medical records, the postmortem pathology report, a tissue sample and perimortem serum analysis — which were obtained through extraordinary measures that Victor’s family took to identify his cause of death.

The researchers note the case study is significant, because few cases of injury and death following vaccination have such extensive medical documentation.

This general lack of documentation is a serious issue, indicating the safety data for the vaccines is incomplete, they wrote.

“This case review and our findings emphasize that without the described thorough investigations, accurate safety data cannot be realized,” they wrote, “and in fact, the safety data is likely impacted by information gaps in the reporting.”

In other words, public health agencies are making their risk-benefit analyses of the vaccines without proper safety data, they said. That safety data is also necessary to provide the public with complete informed consent…