Why Pfizer Can Never Be Trusted
State of the Nation | January 16, 2022
Here is an Announcement from the American Academy of Pediatrics website (May 4, 2021):
“Children ages 2-11 could potentially be eligible for (the still-experimental) COVID-19 vaccine this fall. Pfizer Chairman and CEO Albert Bourla, D.V.M., Ph.D. (Doctor of Veterinary Medicine), said on a quarterly earnings call Tuesday he expects to request (experimental) Emergency Use Authorization (EUA) from the Food and Drug Administration (FDA) in September. Under his plan, an EUA request for ages six months to 2 years would follow in the fourth quarter.
“Pfizer and its partner BioNTech currently are waiting for an FDA decision on an EUA for adolescents ages 12-15 years.”
And here is a list of lawsuits related to sixteen Pfizer drugs that were FDA-approved before long-term safety studies were completed:
(And the CDC Wonders Why There is Such a Thing as “Big Pharma/Big Vaccine-hesitancy”)
List Collated by Gary G. Kohls, MD – March 10, 2021 – (1041 words)
Pfizer is one of the largest multinational drug companies on the planet – and one of the five largest vaccine manufacturers (the other four are Sanofi, Merck, GlaxoSmithKline and Johnson $ Johnson. AstraZeneca is # 10). Pfizer has faced thousands of lawsuits for fraudulent marketing and medical injuries caused by some of its most profitable, drugs.
Pfizer has also set a record for the largest fine paid for a health care fraud lawsuit filed by the U.S. Department of Justice. Pfizer paid $2.3 billion in fines, penalties, and settlement for illegal marketing claims.
Here is a partial list of 13 of Pfizer’s most dangerous, most litigated, most potentially lethal drugs. (NOTE: If any reader had adverse effects to any of the following Pfizer drugs, he/she might want to consult an attorney).
Celebrex,
Bextra,
Geodon,
Zyvox,
Lyrica,
Neurontin,
Protonix,
Prempro,
Chantix,
Depo-Testosterone,
Zoloft,
Effexor,
Feldene,
Viagra,
Lipitor,
Zithromax,
Etc.
Celebrex and Bextra
Prizer promoted its two COX-2 pain relievers Celebrex and Bextra which generated 7000 lawsuits and a $894 million settlement. Both medications were me-too drugs similar to Merck’s infamous Vioxx, which caused 50,000 lawsuits because of cardiovascular deaths and injuries. Merck settled most of the cases with a $4.85 billion settlement.
Geodon, Zyvox, and Lyrica
Pfizer paid $1 billion to resolve allegations under the civil False Claims Act that the company illegally promoted four drugs – Bextra; Geodon, an anti-psychotic drug; Zyvox, an antibiotic; and Lyrica, an anti-epileptic drug – and caused false claims to be submitted to government health care programs for uses that were not medically accepted indications.
Neurontin
Pfizer paid out $142 million for committing racketeering fraud in the marketing of Neurontin.
Protonix
As part of a larger group of proton pump inhibitor lawsuits, Pfizer faced a number of Protonix lawsuits after it acquired drug company Wyeth who had been accused of marketing the drug for unapproved uses. In 2013, Pfizer agreed to pay $55 million to settle illegal marketing claims but the company may still be facing lawsuits for kidney injuries caused by the medication.
Prempro
Nearly 10,000 Prempro lawsuits were filed by women who had been diagnosed with breast cancer. The lawsuits were largely settled by 2012 for about $1 billion.
Chantix
Pfizer faced about 3,000 Chantix lawsuits filed by people who claimed they experienced suicidal thoughts and psychiatric disorders after using Chantix for smoking cessation. Pfizer set aside about $288 million and at least some of the cases were settled.
Depo-Testosterone
Thousands of cases of medical injury due to testosterone replacement therapy have been filed. Other drug companies have paid $ billions to settle their cases, however some Pfizer testosterone lawsuits were dismissed.
Zoloft
About 250 Zoloft lawsuits were filed, claiming Pfizer actively promoted the use of Zoloft to pregnant women despite knowledge of birth defect risks from their research. These cases were largely dismissed in 2016 when a judge concluded that there was not enough evidence to prove a link between birth defects and Zoloft use.
Effexor
Effexor was a medication originally produced by Wyeth which has also been the cause of multiple lawsuits. People who filed Effexor lawsuits claimed that it caused birth defects, and separately, suicidal thoughts and behaviors. In September 2015, Effexor lawsuits were dismissed but may have been eligible to refile.
Lipitor
Pfizer’s drug that lowers cholesterol (but only minimally decreases heart attack risk) but causes serious muscle damage, diabetes and other unforeseen health defects has generated billions of dollars of lawsuits.
Xeljanz
Pfizer’s arthritis and ulcerative colitis drug was only belatedly acknowledged by Pfizer to cause cancer, serious cardiovascular events and venous thromboembolism (such as pulmonary embolism or deep vein thrombosis). Many lawsuits are in progress.
Feldene; Viagra, Zithromax, etc
____________________________________________________________________________________________________________________________
Environmental Pollution
In 1971 the Environmental Protection Agency (EPA) asked Pfizer to end its long-time practice of dumping industrial wastes from its plant in Groton, Connecticut in the Long Island Sound. The company was reported to be disposing of about 1 million gallons of waste each year by that method.
In 1991 Pfizer agreed to pay $3.1 million to settle EPA charges that the company seriously damaged the Delaware River by failing to install pollution-control equipment at one of its plants in Pennsylvania.
In 1994 Pfizer agreed to pay $1.5 million as part of a consent decree with the EPA in connection with its dumping at a toxic waste site in Rhode Island.
In 1998 Pfizer agreed to pay a civil penalty of $625,000 for environmental violations discovered at its research facilities in Groton, Connecticut.
In 2002 New Jersey fined Pfizer $538,000 for failing to properly monitor wastewater discharged from its plant in Parsippany.
In 2003, shortly after Pfizer acquired Pharmacia, the company (along with Monsanto) agreed to pay some $700 million to settle a lawsuit over the dumping of known-to-be-carcinogenic PCBs in Anniston, Alabama.
In 2005 Pfizer agreed to pay $22,500 to settle EPA claims that the company failed to properly notify state and federal officials of a 2002 chemical release from its plant in Groton that seriously injured several employees and necessitated a major emergency response.
Also in 2005, Pfizer agreed to pay $46,250 to settle charges that its Pharmacia & Upjohn operation had violated federal air pollution rules at its plant in Kalamazoo, Michigan.
In 2008 Pfizer agreed to pay a $975,000 civil penalty to resolved federal charges that it violated the Clean Air Act at its former manufacturing plant in Groton, Connecticut in the period from 2002 to 2005.
Environmental groups in New Jersey have criticized as inadequate a clean-up plan devised by Pfizer and the EPA for the American Cyanamid Superfund site in Bridgewater, which is considered one of the worst toxic waste sites in the country. Pfizer inherited responsibility for the clean-up through its 2009 purchase of Wyeth.
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Dr Gary G. Kohls lives in the USA and writes articles that deal with the dangers of fascism, corporatism, totalitarianism, militarism, racism, malnutrition, and Big Pharma’s over-drugging and over-vaccinating agendas. In addition, his columns deal with cultural movements that threaten democracy, war, civility, health, freedom, the future of the children and the sustainability and livability of the planet.
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January 21, 2022 - Posted by aletho | Corruption, Deception, Environmentalism, Science and Pseudo-Science, Timeless or most popular | Pfizer
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Book Review
Shattered Dreams: The HPV Vaccine Exposed (2019)
By Christina England – 30 Q&As – Book Review & Summary
Lies are Unbekoming | September 4, 2026
… Gardasil received FDA fast-track approval in 2006, Cervarix followed in 2009, and Gardasil 9 was approved in December 2014 with more than double the aluminium adjuvant content of the original. The commercial context is specific. Merck was about to lose patent protection on Zocor and faced $18 billion in Vioxx injury claims from a cardiovascular drug the company had marketed while suppressing its own data showing a five-times increase in heart attacks. Analysts projected the global HPV vaccine market at $4 billion by 2011, contingent on government-funded national programs for teenage girls. The 1986 National Childhood Vaccine Injury Act had already granted manufacturers complete liability immunity. By 2013, Japan had withdrawn its HPV vaccine recommendation after cataloguing severe adverse reactions in hundreds of girls. No Western government followed. The establishment position across the UK, US, Australia, and most of Europe held, and still holds, that the vaccines are safe and effective, that reported injuries are coincidental, and that cervical cancer prevention justifies the program. The book was published into this position, not against a vacuum.
Shattered Dreams sits alongside Mary Holland’s The HPV Vaccine On Trial and Viera Scheibner’s foundational vaccination work as part of the documented record on what has been done to a generation of teenage girls under the banner of cancer prevention. The full summary unpacks three specific findings: that Merck used the aluminium adjuvant itself as the “placebo” control in 92.5% of trial subjects, making it structurally impossible to detect excess reactions from the adjuvant; that Dr. Sin Hang Lee found HPV DNA fragments bound to aluminium in every one of sixteen Gardasil samples tested, and in the blood and spleen of a New Zealand girl six months after her third dose; and that in every country with high vaccination coverage, including Australia, the UK, Norway, and Sweden, cervical cancer rates have stopped declining and started rising specifically in the vaccinated cohort. Martínez-Lavín’s 2017 calculation puts the number needed to seriously harm with Gardasil 9 at 140, and the number needed to vaccinate to prevent one case at 1,757. Thirteen young women are seriously harmed for every one who benefits. The vaccine was approved on the basis of trials that could not detect what the trials were supposed to detect, and it is still being given to twelve-year-olds today. … Read full review
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