TruthPirates.com

Surprise... The Pharmaceutical Industry is Not Science!

American pharmaceutical giant Pfizer Inc. and its subsidiary Pharmacia & Upjohn Company Inc. have agreed to pay $2.3 billion, the largest health care fraud settlement in the history of the Department of Justice, to resolve criminal and civil liability arising from the illegal promotion of certain pharmaceutical products, the Justice Department announced today. ...Continue Reading

Bill Gates...not a doctor or a scientist but is somehow front and center of this "Pandemic"... are we to trust this Eugenics supporter with our lives... especially after he said on camera that Vaccines can curb the population?


“The world today has 6.8 billion people. That's heading up to about nine billion. Now if we do a really great job on new vaccines, health care & reproductive health services, we could LOWER that by perhaps 10 or 15 percent.”

-Bill Gates

How can an FDA Approved Drug be Safe & Effective and later on be pulled from the market and deemed Unsafe?



According to the FDA, a “drug is removed from the market when its risks outweigh its benefits. A drug is usually taken off the market because of safety issues with the drug that cannot be corrected, such as when it is discovered that the drug can cause serious side effects that were not known at the time of approval.” The FDA also takes into account the number of people taking a drug being considered for removal so as to not harm those patients. ...Continue Reading



Patients might think the US Food and Drug Administration’s stamp of approval means that a product is the last word on safety, but about a third of the drugs the FDA approved between 2001 and 2010 were involved in some kind of safety event after reaching the market, according to a study published Tuesday in the Journal of the American Medical Association. ...Continue Reading


It took a median of 4.2 years after the drugs were approved for these safety concerns to come to light, the study found, and issues were more common among psychiatric drugs, biologic drugs, drugs that were granted "accelerated approval" and drugs that were approved near the regulatory deadline for approval. ...Continue Reading

When Bayer's Cutter Laboratories realized that their blood products, Factor VIII and IX or antihemophiliac factor (AHF), were contaminated with human immunodeficiency virus (HIV), the financial investment in the product was considered too high to destroy the inventory. Cutter misrepresented the results of its own research and sold the contaminated AHF to overseas markets in Asia and Latin America without the precaution of heat treating the product recommended for eliminating the risk. As a consequence, hemophiliacs who infused the HIV-contaminated Factor VIII and IX tested positive for HIV and developed AIDS. ...Continue Reading

In 1945 the US Food and Drug Administration (FDA) approved DDT for public insecticide use. By the end of the same year, American chemical companies were producing an estimated two million pounds of DDT a month. As a result of a vast surplus, negligent regulation, and antiquated scientific tools that inaccurately concluded that DDT had no effect on mammals, DDT found its way into vast amounts of products. However, in 1972 the US Environmental Protection Agency (EPA) banned DDT after conclusive evidence exhibited that it threatened the maturation of birds and caused nervous disorders and cancer in exposed human populaces. ...Continue Reading