by Brian Shilhavy
Editor, Health Impact News
Tens of thousands of mothers are suing the makers of Tylenol for using the popular over-the-counter pain reliever during pregnancy, which resulted in them giving birth to babies diagnosed with autism.
Tens of thousands of mothers are suing the makers of Tylenol in a class-action lawsuit that claims its use during pregnancy led babies to be born with autism.
A study from the NIH found that pregnancy exposure to acetaminophen, the main ingredient in Tylenol, may increase a child’s risk for autism and ADHD.
Karleen DeGroodt is among the mothers in the lawsuit and discussed her use of Tylenol during pregnancy and her son’s autism during an appearance on NewsNation’s “Prime.” (Full article.)
Last October, a federal judicial panel consolidated dozens of these lawsuits alleging that acetaminophen, the active ingredient in Tylenol and generic versions of the drug, can cause autism spectrum disorder and attention deficit hyperactivity disorder.
TorHoerman Law is one of the law firms representing these mothers, and they have produced the following video explaining the lawsuit.
The main defendant in the lawsuit is Kenvue, which is the former Johnson & Johnson’s consumer health unit that is now a “spin-off” of J&J. (Source)
Co-defendants in the lawsuit are CVS Health, Rite Aid Corp, Safeway Inc, Target Corp and Walgreens Boots Alliance, which are being charged with failing to warn consumers about the risks of Tylenol.
Kenvue has suffered some setbacks in recent weeks in trying to get some of the lawsuits dismissed, with one of the reasons given to dismiss the lawsuits being that the FDA had approved the product and its labels.
Kenvue Inc cannot immediately appeal a federal judge’s order allowing lawsuits claiming that its popular over-the-counter painkiller Tylenol can cause autism in children of mothers who take it during pregnancy, the judge has ruled.
U.S. District Judge Denise Cote in Manhattan on Thursday ruled that Kenvue, formerly Johnson & Johnson’s consumer health unit, had not shown any basis for allowing the unusual step of an appeal to the 2nd U.S. Circuit Court of Appeals before final judgment in the case.
In April, Cote denied Kenvue’s motion to dismiss one of the lawsuits on the grounds that the U.S. Food and Drug Administration’s approval of Tylenol’s label preempted any state law claims. Had she ruled in the company’s favor, it would have ended the entire litigation. (Source.)
The amount of studies published in the medical journals linking Tylenol taken during pregnancy to babies born with autism is overwhelming.
Here are just a couple of the more recent studies published this year (2023).
Acetaminophen causes neurodevelopmental injury in susceptible babies and children: no valid rationale for controversy
Clinical and Experimental Pediatrics – June 14, 2023
Abstract
Despite worldwide acceptance of acetaminophen as a necessary medicine in the field of pediatrics, evidence that early life exposure to acetaminophen causes neurodevelopmental injury in susceptible babies and children has mounted for more than a decade.
Evidence is diverse, including extensive work with laboratory animals, otherwise unexplained associations, factors associated with the metabolism of acetaminophen, and some limited studies in humans. Although evidence has reached an overwhelming level and has been reviewed in detail recently, some controversy remains. In this narrative review, some of those controversies are evaluated.
Evidence from the prepartum and the postpartum period is considered, avoiding controversies raised by considering only the limited evidence pointing exclusively toward risks during the prepartum period. Among other issues, the associations through time between acetaminophen use and the prevalence of neurodevelopmental disorders are considered.
A systematic review reveals that the use of acetaminophen in the pediatric population was never tracked carefully, but historical events that affected use of the drug were documented and are sufficient to establish apparent correlations with changes in the prevalence of neurodevelopmental disorders.
In addition, problems with exclusive reliance on results from meta-analyses of large datasets and from studies involving small time frames of drug exposure are reviewed. Further, evidence demonstrating why some children are susceptible to acetaminophen-induced neurodevelopmental injury is examined.
It is concluded that, at least among the factors considered, there is no valid rationale for controversy regarding the conclusion that early life exposure to acetaminophen causes neurodevelopmental injury in susceptible babies and small children. (Source.)
The use of acetaminophen in pregnancy: a double whammy
Annals of Medicine and Surgery – March 14, 2023
Abstract
Acetaminophen is the most widely over the counter used analgesic in the world, and the World Health Organization advises using it as first-line treatment for pain issues (WHO).
However, various side effects have been documented with its use such as nausea, vomiting, constipation at low doses whereas in large doses, it might even result in hepatoxicity.
Recent literature suggests that the use of acetaminophen in pregnancy even in optimal doses could result infant being born with ADHD and autism, so in this short communication we talk about the prevalence of neurodevelopment disorders in infants as a result of its use, as well as shed light to the measures that should be adopted to minimize the adverse effects. (Source.)
We have been publishing articles exposing the dangers of Tylenol for over a decade now. A search on Health Impact News for this killer drug, which is available as an over-the-counter (OTC) drug that even minors can purchase in their local pharmacy or retail store will result in over 80 articles.
Pregnant women are the not the only ones who should immediately STOP using this killer drug. NOBODY should be using it.
Tylenol is a classic example of how corporate profits from the pharmaceutical drug companies are far more important than patient safety, as millions of lives are sacrificed to keep these drugs on the market.
It is also just another example of how the FDA works to protect pharmaceutical companies, and NOT consumers.
Tylenol has been on the market for 75 years bringing in annual revenues that exceed $300 million.
And the adverse effects from Tylenol have been widely published for over a decade now.
In 2013 ProPublica published one of the most comprehensive reviews of Tylenol’s toxic side effects:
About 150 Americans a year die by accidentally taking too much acetaminophen, the active ingredient in Tylenol. The toll does not have to be so high.
During the last decade, more than 1,500 Americans died after accidentally taking too much of a drug renowned for its safety: acetaminophen, one of the nation’s most popular pain relievers.
Acetaminophen – the active ingredient in Tylenol – is considered safe when taken at recommended doses. Tens of millions of people use it weekly with no ill effect. But in larger amounts, especially in combination with alcohol, the drug can damage or even destroy the liver.
Davy Baumle, a slender 12-year-old who loved to ride his dirt bike through the woods of southern Illinois, died from acetaminophen poisoning. So did tiny five-month-old Brianna Hutto. So did Marcus Trunk, a strapping 23-year-old construction worker from Philadelphia.
The toll does not have to be so high.
The U.S. Food and Drug Administration has long been aware of studies showing the risks of acetaminophen – in particular, that the margin between the amount that helps and the amount that can cause serious harm is smaller than for other pain relievers. So, too, has McNeil Consumer Healthcare, the unit of Johnson & Johnson that has built Tylenol into a billion-dollar brand and the leader in acetaminophen sales.
Yet federal regulators have delayed or failed to adopt measures designed to reduce deaths and injuries from acetaminophen overdose, which the agency calls a “persistent, important public health problem.”
The FDA has repeatedly deferred decisions on consumer protections even when they were endorsed by the agency’s own advisory committees, records show. (Full article.)
Health Impact News has published stats on Tylenol deaths in the past, and other reports actually put the death toll much higher than the stats ProPublica used from the CDC in 2013.
A 2004 published study took statistics from poison control centers around the U.S. and found “458 deaths due to acute liver failure each year.”
In 2013 we published an article about a study by Dr. William Shaw which was published in the Journal of Restorative Medicine that linked Tylenol use in children, and especially in conjunction with childhood vaccines, led to an increase in autism. See:
Study: Evidence that Acetaminophen, Especially in Conjunction with Vaccines, is a Major Cause of Autism and Asthma
In 2016, Jennifer Margulis reported on many more studies that showed how dangerous Tylenol was to treat fever and pain in small children.
Acetaminophen (Tylenol) Harmful for Babies
Some of the other published studies documenting how deadly Tylenol is:
- Acetaminophen kills almost 500 people a year due to acute liver failure. (Source.)
- Acetaminophen overdose is the leading cause for calls to Poison Control Centers – more than 100,000/year. (Source.)
- Acetaminophen accounts for more than 56,000 emergency room visits, 2,600 hospitalizations. (Source.)
- Acetaminophen poisoning causes nearly 50% of all acute liver failure in the United States. (Source.)
- Acetaminophen is linked to fatal skin reactions. (Source.)
- Acetaminophen causes a two-fold increased risk of blood cancer. (Source.)
- Acetaminophen can cause an increase in autism, attention deficit with hyperactivity, and asthma when used with vaccines. (Source.)
And yet, any child can walk into a drug store or grocery store and buy it like candy.
Those manufacturing and selling this dangerous OTC drug have escaped prosecution for many years now, and Big Pharma’s pockets are very deep, deep enough to buy any judge they want.
So I do not expect much to happen with this current class action lawsuit by mothers who have suffered in seeing their babies born with neurological diseases due to using Tylenol.
It is up to YOU to stay informed. Only you can protect your family and loved ones from the criminal drug cartels and their control of the U.S. Government, especially the FDA and CDC.
Those criminal activities that include mass murder did NOT begin with COVID. There are still a few of us around who have been exposing these criminals for decades now.
Many of the new “leaders” of the health freedom movement that have become popular since COVID are still drug and vaccine pushers, and many of them now are fighting “turf wars” with each other so they can sell you their own drugs and vaccines that they will claim are “safer”.
There are no such things as “safe” vaccines. And to promise to manufacture “safe vaccines” in the future means they believe in sacrificing children to the vaccine gods in vaccine trials.
JUST SAY NO TO PHARMACEUTICAL DRUGS!
See Also:
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Jesus Would be Labeled as “Antisemitic” Today Because He Attacked the Jews and Warned His Followers About Their Evil Ways
Insider Exposes Freemasonry as the World’s Oldest Secret Religion and the Luciferian Plans for The New World Order
Identifying the Luciferian Globalists Implementing the New World Order – Who are the “Jews”?
The Brain Myth: Your Intellect and Thoughts Originate in Your Heart, Not Your Brain
Fact Check: “Christianity” and the Christian Religion is NOT Found in the Bible – The Person Jesus Christ Is
Was the U.S. Constitution Written to Protect “We the People” or “We the Globalists”? Were the Founding Fathers Godly Men or Servants of Satan?
The Seal and Mark of God is Far More Important than the “Mark of the Beast” – Are You Prepared for What’s Coming?
The Satanic Roots to Modern Medicine – The Mark of the Beast?
Medicine: Idolatry in the Twenty First Century – 8-Year-Old Article More Relevant Today than the Day it was Written
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