COVID-19 Vaccine Harm Data Reveals Concerning Patterns
Pfizer and Moderna COVID-19 vaccines seem to have four levels of harm intensity that are based on batch number, says former pharmaceutical executive, Sasha Latypova.
“They’re dependent on the letters used in the alphanumeric numbering, which should be just random,” Latypova told The Epoch Times.
“We have variability of toxicity, but it’s also aligned in three patterns—high, medium, and low. And the fourth one, something as apparent as placebo.”
She cited two publications that point to this conclusion.
One was a research letter submitted by Danish scientists to the peer-reviewed European Journal of Clinical Investigation. Max Schmeling, lead author of the letter, used data obtained from the Danish government to map out Pfizer’s mRNA COVID-19 vaccine batches versus the adverse events they caused.
Schmeling found that the batches fell into three distinct levels of harm. There were nine “high” batches in Denmark that caused thousands of suspected adverse events per batch (blue). There were 25 “medium” batches that were less toxic (green). And there were 12 “low” batches that seemed to cause very few adverse events (yellow).
A French genomics statistician, Herve Seligmann, tried to reproduce this study using a grassroots database that matched adverse events to batch numbers. He got similar results.
The Danish scientists also noted that some batches caused adverse events that were severe, while other batches had milder adverse events. Larger vaccine batches tended to have lower rates of adverse effects than smaller batches. So when more doses were produced in a single batch, the rate of adverse effects per 1,000 doses was generally lower.
This is a highly unusual situation. According to the standards set by the U.S. Food and Drug Administration, a pharmaceutical product should not have a high variation of adverse events from batch to batch.
Both Moderna and Pfizer COVID-19 vaccines have failed to meet this safety standard, said Latypova. In addition to all this, the figure above shows three clean trendlines, with no noise in between.
“Meaning that this is not actually random, it’s by design,” said Latypova.
In other words, the differences in the rates of adverse events are not likely to be random, but rather point to underlying factors related to the vaccine batches themselves.
Latypova is an expert in drug safety and manufacturing. She has been independently monitoring COVID-19 vaccines since their rollout using publicly available data.
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