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Public Health and Medical Professionals for Transparency: Pfizer’s COVID-19 vaccine biological product file

re: ethics in medicine

Real science is never settled, and anyone who has certainty on such things is not qualified to discuss it.

The FDA wants to slow-walk the Pfizer documents for COVID vaccines, taking 55 years to release all of it. No rational person can look at that delay, without at least wondering whether fraud and corruption are at work. I smell a rat.

Personally, I’m very flexible on this, and am willing to give the FDA 55 days to release all of it. If Pfizer and Moderna and their ilk get blanket immunity for side effects along with tens of billions in prepaid orders and profits, a government working for you and me would require that they agree to release all documents instantly. But the FDA and CDC are de facto controlled by Big Pharma, so the full data dump will likely never see the light of day in my lifetime*.

* Although a freshened-up ruling class could get it done overnight and maybe nationalize the vaccine program for good measure. While we’re at it, a windfall profits tax on Big Pharma gravy-train profits would be justified, given the near-zero risk taken on by Big Pharma—nothing remotely approaching a free market capitalism system.

Public Health and Medical Professionals for Transparency

Four days after the Pfizer vaccine was approved for ages 16+, we submitted a Freedom of Information Act Request to the FDA for all of the data within Pfizer’s COVID-19 vaccine biological product file. We have now sued the FDA for not releasing the data. Click below for court documents and for productions of Pfizer’s documents from the FDA.

...

WIND: I don’t have much hope for the lawsuit. Pfizer has armies of lawyers and they’ve been successful at delaying previous lawsuits for years, even if ultimately losing.

Below is one of the first released documents. I’m in no position to understand the significance of the huge number of side effects. And it is only through February 2021. You have to compare the AE’s (Adverse Events) against a baseline, and ideally against a control group (which Pfizer and Moderna have dissolved, how convenient for them).

5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021

Total Number of BNT162b2 Adverse Events by System Organ Classes and Event Seriousness
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