Tag: pfizer

HIDDEN PFIZER TRIAL DATA SHOWS THAT ALL “VACCINATED” WOMEN IN PREGNANCY LOST THEIR UNBORN BABIES

A lawsuit filed by Public Health and Medical Professionals for Transparency produced documents from Pfizer showing that its Wuhan coronavirus (Covid-19) “vaccine” caused all of the pregnant mothers on whom it was tested to miscarry.

Entitled, “Cumulative Analysis of Post-authorization Adverse Event Reports,” a report from Pfizer describing events reported up to February 2021 – you can download that report – shows that not a single pregnant woman who took the Pfizer jabs delivered a live baby.

Table 6 of the report, titled “Missing Information,” reveals under the first topic of “Use in pregnancy and lactation” the following statement:

“Pregnancy outcomes for the 270 pregnancies were reported as spontaneous abortion (23), outcome pending (5), premature birth with neonatal death, spontaneous abortion with intrauterine death (2 each), spontaneous abortion with neonatal death, and normal outcome (1 each). No outcome was provided for 238 pregnancies (note that 2 different outcomes were reported for each twin, and both were counted).”

Taken at face value, this would suggest that of 270 pregnancies, there were 23 spontaneous abortions, five “outcomes pending,” two premature births with neonatal death, two spontaneous abortions with intrauterine death, one spontaneous abortion with neonatal death, and one normal outcome. However, there is also that tricky statement: “no outcome was provided for 238 pregnancies.”

“So really we have no idea what happened with 243 (5 + 238) of the pregnancies of these injected women; they have just not been included in the report,” reported Principia Scientific International.

“What we do know is that of 27 reported pregnancies (270 subtract 243), there are 28 dead babies! This appears to mean that someone was pregnant with twins and that 100 percent of the unborn babies died.”

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COVID COVER-UP: Pfizer INTERFERES Just Days Before Massive FOIA Vaccine Data Drop, FDA Claims The Vaccine Manufacturer Must Help Review and Redact Documents Before Public Release

Who does the US FDA answer to? Well, apparently it’s Pfizer, the German-based Big Pharma megalith.

Just days before the FDA was set to release over 12,000 documents related to the experimental Covid-19 vaccines, Pfizer asked a federal court to allow it to intervene before any information is released to the public.

Unsurprisingly, the FDA wholeheartedly agreed, asking the court to allow the vaccine maker to ‘help’ curate the documents, which would also buy the agency more time to release the much anticipated, and likely damning, data.

Conflict of interest? What’s that?

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Facebook’s fake fact-checkers censor medical journal article on alleged safety issues with Pfizer Covid-19 vaccine study

This is a dangerous time, indeed, when self-proclaimed fact checkers and curators are permitted to control information in the name of what they claim is the public good.

This trend was relatively unheard of prior to 2016. Until that time, the shaping and censoring was largely done in an invisible way. Nobody admitted to it because the public wouldn’t have stood for it.

But a successful propaganda campaign I’ve described in my books The Smear and Slanted aimed to convince many in the public to accept third parties telling us what we can cannot know or see.

Obviously, corporate and political interests are behind the efforts, using them to keep the public from seeing or hearing information that is contrary to their paid interests.

This helps explain a lot about Facebook’s indefensible censorship of a factual investigation published in the prestigious British Medical Journal.

The article by Paul Thacker exposed alleged poor practices and quality control issues during Pfizer’s Covid-19 vaccine studies based on whistleblower documentation.

According to the article:

A regional director who was employed at the research organisation Ventavia Research Group has told The BMJ that the company falsified data, unblinded patients, employed inadequately trained vaccinators, and was slow to follow up on adverse events reported in Pfizer’s pivotal phase III trial. Staff who conducted quality control checks were overwhelmed by the volume of problems they were finding. After repeatedly notifying Ventavia of these problems, the regional director, Brook Jackson, emailed a complaint to the US Food and Drug Administration (FDA). Ventavia fired her later the same day. Jackson has provided The BMJ with dozens of internal company documents, photos, audio recordings, and emails.

Paul Thacker, British Medical Journal

Of course this bombshell information is not what vaccine industry interests and their supporters in government and media wanted to be seen. (Pfizer has always denied any wrongdoing. Pfizer, the FDA and CDC all say all vaccines in use in the U.S. are safe and effective.)

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