Pfizer's 'Post-Marketing Surveillance Report' Reveals That Pfizer Manipulated Data And Wrongly Tabulated Adverse Events, Which Concealed Them.

We saw that Pfizer manipulated data by setting various different "Thresholds" for counting adverse events in each SOC. In addition, Pfizer frequently assigned adverse events to SOCs that were inappropriate, which obscured adverse event signals.

Why did the Hematological SOC have a threshold of 15 adverse events occurring before a diagnosis was named even as the Neurological SOC had a threshold of only two adverse events, which allowed Pfizer to leave out 20 adverse events' diagnoses? Such a large difference in the number of adverse events required for them to be assigned a diagnosis seems inexplicable - unless Pfizer was attempting to lessen the number of vaccine-related medically significant outcomes.

All 300 adverse events in the Stroke SOC were serious; but again, because of the threshold of greater than one occurrence, only 292 adverse events were listed, leaving eight serious adverse events undisclosed.

Due to the threshold criteria of 15 or more adverse events sharing the same diagnosis, 192 adverse events were not included in this SOC's enumeration of adverse events.

The Cardiovascular SOC excluded 25 cases of myocarditis and 32 cases of pericarditis, which are inherently cardiac events, and Pfizer instead reported them in the Immune-Mediated/Autoimmune SOC. By reporting those in a seemingly unrelated SOC, Pfizer decreased the cardiovascular disease signal and prevented quick review of all cardiac-related adverse events.

Despite approximately 6,000 serious adverse events under Figure 1's "Gastrointestinal" category, Pfizer did not create a Gastrointestinal SOC. Seventy gastrointestinal cases were reported in the Hepatic SOC. While the liver is part of the overall gastrointestinal system, where are the thousands of other gastrointestinal serious adverse events? The Hepatic SOC is also an anomaly because it only includes one diagnosis, "liver injury.

The 376 seizure events in the Neurological SOC made up 69% of the total neurological adverse events, and half of the neurological adverse events occurred within one day post-injection. 

https://dailyclout.io/pfizers-post-marketing-surveillance-reveals-pfizer-manipulated-data/