Global Pharma's eye drops have been linked to a U.S. outbreak which has led to at least five people losing their vision.

Author Naomi Wolf, who has been coordinating an analysis of the Pfizer documents about their Covid vaccine, reveals astounding discoveries today — namely that Pfizer and the FDA had extensive knowledge of devastating side effects from their vaccine, including deaths, paralysis and stroke-like symptoms. Stay tuned as Wolf will be returning with more info. Lawsuits […]

The Gateway Pundit previously reported — Texas Northern District Judge Mark Pittman made the decision to release documents after the group behind the FOIA request, Public Health and Medical Professionals for Transparency, filed a joint status report.   The FDA then reached an agreement with the government on how fast the documents will be produced. The… The post FDA Releases Thousands of Pages of Documents Related to the Experimental Covid-19 Vaccines through FOIA Request — Animal Studies Showed Adverse Affects appeared first on The Gateway Pundit .

Project Veritas on Wednesday released part two of a two-part “Expose FDA” series. FDA Executive Officer Chris Cole told an undercover Project Veritas journalist all about the agency’s close ties with the pharmaceutical companies. “The drug companies, the food companies, the vaccine companies. So, they pay us hundreds of millions of dollars a year to… The post Project Veritas: FDA Executive Officer Exposes Close Ties Between Agency and Pharmaceutical Companies (VIDEO) appeared first on The Gateway Pundit .

The Food and Drug Administration (FDA) has restored a document outlining why it approved Moderna’s COVID-19 vaccine, days after the regulatory agency pulled the 30-page file offline after receiving questions about it from The Epoch Times. No explanation has been given for why the document vanished hours after the questions were sent, but the removal […]

FDA Asks Court To Delay First 55K Batch Of COVID Docs; Pfizer Moves To Join Case Authored by attorney Aaron Siri via Injecting Freedom (emphasis ours), As explained in prior posts , in a lawsuit seeking all of the documents the FDA relied upon to license Pfizer’s COVID-19 vaccine, a federal judge shot down the FDA’s requested rate of 500 pages per month and instead ordered the FDA to produce at the rate of 55,000 pages per month starting on March 1.  Since the government has trillions of dollars of our money, it is putting it to good use by fighting to assure that the public h [...]

Cytalux (pafolacianince), a drug that binds to ovarian cancer tissue and glows when exposed to fluorescent light, has been approved by the U.S. Food and Drug Administration (FDA) to help surgeons detect ovarian tumors during surgical procedures in patients.

"Wait, What?" Even Reuters Tripping Out On 55-Year Delay To Release Pfizer Vax Data Last week attorney Aaron Siri of Injecting Freedom reported that the FDA is going to take 55 years , or until 2076, to disclose all of the data and information it relied on before approving Pfizer's Covid-19 vaccine. The Food and Drug Administration (FDA) headquarters in White Oak, Maryland, August 29, 2020. REUTERS/Andrew Kelly Following its publication, we expected the usual constellation of conflicted neerdowell 'fact checkers' to shoot it down - or at least, spin what was going on. To our sur [...]

The best moments from today’s 8 hour FDA Vaccine hearing. ‘The Vaccines are driving the Variants’… BOMBSHELL Info During Todays FDA Vax Meeting Dr Rose States Based on The VAERS Data… The Risks Far Outweigh The Benefits Especially For Children Over A 1000% Increase In Adverse Events In 2021! Questions If The Shots Are Driving […] The post FDA Committee Goes Rouge, Exposes Everything Going Wrong With Vax appeared first on Populist Press 2021 © .

A federal advisory panel said Friday the Food and Drug Administration (FDA) should not approve a third booster dose of Pfizer and BioNTech's COVID-19 vaccine for everyone 16 or older, but indicated they would be open to b...