The stunning secret behind the thousands of Xarelto lawsuits

by Jon Rappoport

May 8, 2017

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Welcome to the circus, boys and girls. Parades, animals, acrobats, clowns, all colluding to approve lethal drugs for public use! Watch people take the drugs and fall down, watch them carted off in colorful cars to hospitals, where the doctors will have no idea what’s causing the life-threatening injuries! It’s wild, it’s crazy, and it’s brought to you by drug companies and their enablers at the FDA! It’s all covered by insurance. We’ve got cotton candy, popcorn, ice cream for the kiddies, and everybody can get in under the big tent! It’s the biggest game and the biggest hustle in town!

Recently, I wrote about the 18,000 lawsuits against Xarelto. Here is a quick recap:

The first court test of Bayer/J&J’s billion-dollar bonanza, blood-thinner, Xarelto, is coming up in New Orleans next week. The outcome will influence how the 18,000 lawsuits behind it will be handled.

The plaintiff in the first suit is Joseph Boudreaux. “While Xarelto was supposed to help cut his stroke risk, Boudreaux says it instead caused internal bleeding that required a week-long hospital stay in the intensive-care unit, several blood transfusions and multiple heart procedures. ‘I don’t want anybody else to suffer like I have from that drug,’ the part-time security guard says,” reports the Chicago Tribune.

Lawyers for Bayer and J&J will argue, in the main, that Xarelto was approved by the FDA as safe and effective.

This is the normal front-line strategy. “Well, the government says our drug is safe and effective, so what else do you want from us? We’ve done our duty. We’re off the hook.”

All right, that’s my recap.

BUT suppose the drugmaker and the government (FDA) both cheated and lied and committed multiple crimes, during the clinical trials of the drug leading up to its approval for public use?

It turns out someone has been investigating those clinical trials of Xarelto, and he has uncovered stunning secrets. His name is Charles Seife. He is a professor of journalism at New York University.

Lawyers for the plaintiffs in the 18,000 lawsuits against Xaraelto, take notice. This is information you want to have at your fingertips. Seife can provide many details—here I’m just presenting his overview.

Buckle up.

Professor Seife writes, at Slate, about the four human clinical trials of Xarelto. These were called the RECORD trials; RECORD 1, 2, 3, and 4:

“The problems were so bad and so widespread that, contrary to its usual practice, the FDA declared the entire RECORD study to be ‘unreliable.’ Yet if you look in the medical journals, the results from RECORD 4 sit quietly in The Lancet without any hint in the literature about falsification, misconduct, or chaos behind the scenes. This means that physicians around the world are basing life-and-death medical decisions on a study that the FDA knows is simply not credible.”

Seife is pointing out that the FDA never alerted The Lancet that the published report on the Xarelto clinical trials was false through and through.

Seife continues: “RECORD 2, for example, was nearly as awful as RECORD 4: Four out of 10 sites that the FDA inspected showed evidence of misconduct, or other issues grave enough to render the site’s data worthless—including clear evidence of data falsification at one site. In aggregate, these problems raise serious doubts about the quality of all four key rivaroxaban (Xareltio) studies—and, by extension, doubts about how seriously we should take the claim that rivaroxaban is safe and effective. The FDA is keeping mum, even as wrongful-death lawsuits begin to multiply.”

“The sworn purpose of the FDA is to protect the public health, to assure us that all the drugs on the market are proven safe and effective by reputable scientific trials. Yet, over and over again, the agency has proven itself willing to keep scientists, doctors, and the public in the dark about incidents when those scientific trials turn out to be less than reputable. It does so not only by passive silence, but by active deception.”

Basically, Seife is stating that the FDA found horrendous distortions in the clinical trials of Xarelto—and yet the agency approved the drug, as safe and effective, for public use.

—And then people taking the drug began to experience dire “adverse effects,” like uncontrolled bleeding.

And now we have 18,000 lawsuits against Xarelto’s parents, Bayer and J&J.

What about lawsuits against the FDA? That’s a tougher hill to climb for lawyers. Because the FDA is “the government.”

I’ve written many articles about the criminal agency called the FDA (article archive here). For stark revealing light, consider an interview relentless medical reporter, Martha Rosenberg, conducted with an FDA employee, whose job was reviewing new drugs and offering an assessment of their safety and efficacy, prior to agency approval or rejection.

Here is what I wrote in one piece:

In a stunning interview with Truthout’s Martha Rosenberg, former FDA drug reviewer, Ronald Kavanagh, exposes the FDA as a relentless criminal mafia protecting its client, Big Pharma, with a host of mob strategies.

Kavanagh: “…widespread [FDA] racketeering, including witness tampering and witness retaliation.”

“I was threatened with prison.”

“One [FDA] manager threatened my children…I was afraid that I could be killed for talking to Congress and criminal investigators.”

Kavanagh reviewed new drug applications made to the FDA by pharmaceutical companies. He was one of the holdouts at the Agency who insisted that the drugs had to be safe and effective before being released to the public.

But honest appraisal wasn’t part of the FDA culture, and Kavanagh swam against the tide, until he realized his life and the life of his children was on the line.

That’s what I wrote, and considering what has happened in the case of Xarelto, Kavanagh’s statements take on very specific meaning:

The FDA colludes with a drug manufacturer to hide the dangers of a new drug that should never have been approved.

The drug is approved.

The drug assaults people and causes grievous harm.

Based on this article, and many others I’ve written exposing the FDA, I would say the agency is in charge of internal and domestic chemical warfare against the American people.

There. Is that clear enough?

Update—the first lawsuit against Xarelto, in New Orleans, has just been decided by a jury. They have ruled in favor of the drug companies, Bayer and J&J, and against the plaintiff, Joseph Boudreaux.

The major (narrow) issue in the case seems to have come down to this: did the drug companies failed to warn physicians about bleeding risks associated with Xarento?

The jury said Bayer and J&J DIDN’T FAIL TO WARN.

End of story.

The madness continues.

This is what happens when plaintiffs’ lawyers are too dim to see the big picture I presented in this article—or when a presiding judge keeps denying the right to introduce relevant evidence against a drug.

What about the 18,000 Xarelto lawsuits against Bayer and J&J that are waiting in the wings? Right now, the plaintiffs’ lawyers are scrambling to re-think their strategies.

It’s possible that, eventually, all 18,000 cases will be settled, not tried in court. If that happens, the people who have been damaged by Xarelto could each receive a minimal payout for their suffering.

NOTE TO PLAINTIFFS’ LAWYERS: Reveal, in court, the criminal collusion between the FDA and Bayer and J&J. Expose the crimes they committed in order to get the highly dangerous Xarelto approved for public use in the first place—when it should have been rejected and all the stocks destroyed.

Put THAT in front of a jury.


Exit From the Matrix

(To read about Jon’s mega-collection, Exit From The Matrix, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

Blood-thinning drug Xarelto faces 18,000 lawsuits

by Jon Rappoport

April 26, 2017

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The first court test of Bayer/J&J’s billion-dollar bonanza, blood-thinner, Xarelto, is coming up in New Orleans next week. The outcome will influence how the 18,000 lawsuits behind it will be handled.

The plaintiff in the first suit is Joseph Boudreaux. “While Xarelto was supposed to help cut his stroke risk, Boudreaux says it instead caused internal bleeding that required a week-long hospital stay in the intensive-care unit, several blood transfusions and multiple heart procedures. ‘I don’t want anybody else to suffer like I have from that drug,’ the part-time security guard says,” reports the Chicago Tribune.

Lawyers for Bayer and J&J will argue, in the main, that Xarelto was approved by the FDA as safe and effective.

This is the normal front-line strategy in cases where the drugmaker believes it can’t be accused of purposely concealing a medicine’s dangers from the FDA.

“Well, the government says the drug is safe and effective, so what else do you want from us? We’ve done our duty. We’re off the hook.”

It’s called shift the responsibility.

The last time I looked, the FDA doesn’t develop, manufacture, and sell drugs. Pharmaceutical companies do. If their drugs kill people and maim them, why shouldn’t they shoulder the blame, regardless of what a government agency says?

A simple change in law would remedy this situation: irrespective of what the FDA claims or doesn’t claim, ultimate accountability for a drug’s effects lies with the company that created it.

If you own a business that makes a product, and 18,000 people are lined up to sue you because they claim the product seriously harmed them, you’re the one who’s going to have to go to court and try to defend your actions.

You’re not going to be able to claim it was your second cousin’s fault or the man in the moon’s responsibility.

Even if we assume the FDA is honest and thorough and honorable (laughable, I know), they’re simply offering their assessment. It doesn’t matter that they’re the only body that can certify a drug for public use. That’s not a reason to exonerate a drug company.

Drug companies try to make hay from the fact that the FDA is certifying their medicines. “Don’t blame us. The FDA liked our drug. Blame them. And good luck with that.”

This would be like a mother saying, “Yes, I was in the park with my child, and yes, I wandered away to talk to an ice cream vendor, and I came back a half hour later to find her with a broken leg, but you see, it was my husband’s fault. He decided I would be competent to take care of our children…”

Forget all about the clinical trials of new drugs, and the published studies, and the back-and-forth between the pharmaceutical company and the FDA, and the FDA certifications.

It’s far simpler. It’s the sign in the store that says, “You break it, you pay for it.”

You break people, you pay.

The only ones who don’t understand that are criminals.


Exit From the Matrix

(To read about Jon’s mega-collection, Exit From The Matrix, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

NoMoreFakeNews Exclusive: lawyers’ emails revealed in the Monsanto vs. Maui lawsuit

Monsanto/Dow still refuse to open up secret court documents

by Jon Rappoport

April 23, 2015

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Think about it. You’re locked in a high-stakes lawsuit against major corporations, and you can’t see document-material the corporations have filed in order to make their argument with the Judge.

The Judge has seen the redacted blacked-out material, and she will, in part, base her ruling in the case on it. There is no jury.

But you can’t see the blacked-out material, you can’t argue your position with full knowledge.

Welcome to a rigged process.

As my readers know, I exposed the fact that, in the Monsanto/Dow vs. Maui lawsuit, the corporations filed documents with the court that contained large amounts of blacked-out redacted material.

The lawyers representing the people, whose vote to block Monsanto/Dow experiments in Maui was suspended by this lawsuit, have not yet seen those redacted lines and paragraphs.

Therefore, they can’t argue their case from full knowledge.

In the last few days, one of the lawyers, Sharon Kim, who represents the Shaka Movement against Monsanto/Dow, made a request to Nick Kacprowski, a lead attorney for Monsanto/Dow, to see the redacted material (Case 1:14-cv-00511-SOM-BMK Document 5-3 Filed 11/13/14: Declaration of Sam Eathington [Vice President of Global Plant Breeding, Monsanto]).

Their exchange of emails concludes with Kacprowski writing:

“We should note that nothing in this message should be construed as conceding that Shaka has any right to access the sealed information. For example, Plaintiffs [Monsanto, Dow, and others] are concerned by the hostility that Shaka has shown toward the [GMO] seed companies in the past and thus by the risk that it will use this confidential and sensitive information publicly for improper purposes.”

Absurd. How Shaka “would use this material” is a speculative hypothetical. The material’s relevance to the lawsuit can only be assessed by allowing Shaka’s lawyers to read it.

The Judge in the federal case, Susan Oki Mollway, should long ago have ordered that the redactions be removed.


Here is the email exchange. The first email is from attorney Sharon Kim, representing the Shaka Movement. The reply is from Nick Kacprowski, representing Monsanto/Dow. His reply is dense with legalese, but you’ll get the point of it.

Nick,

This email is serves as a request for unredacted copies of the documents that were filed under seal in Civ No. 14-00511. As you are aware, our Opening Brief for the Ninth Circuit Appeal is due on April 30, 2015, and we need the unredacted documents to aid in the preparation of our Opening Brief. Thus, we are requesting copies of the unredacted documents by Wednesday, April 22nd. Please let me know if you have any questions.

Thanks,
Sharon

Sharon A. Lim
Bays Lung Rose & Holma

From: Nick Kacprowski […]
Sent: Tuesday, April 21, 2015 5:02 PM
To: Sharon A. Lim […]
Subject: Re: Ito v. County of Maui

Dear Sharon:

This will respond to your request that Plaintiffs provide Shaka with unredacted versions of the sealed documents in this case by April 22. As you know, Plaintiffs have filed a Motion to Vacate the Expedited Briefing Schedule on your appeal, Case No. 15-15641. As our motion notes, your appeal of the preliminary injunction order will be mooted when the Court rules on the merits of the pending summary judgment motion, which it has indicated it will do by the end of June. If the Ninth Circuit grants the Motion to Vacate, Shaka will have no need for the unredacted documents in the near future, and possibly never, in order to pursue an appeal in this case.

Our proposal is that the parties stipulate to a protective order that provides that the sealed documents will remain sealed, without access for Shaka, unless the Ninth Circuit denies Plaintiffs’ motion that the briefing schedule should be vacated in Case No. 15-15641. It makes sense to defer Shaka’s request to access the sealed documents given that: 1) the sealed documents contain highly sensitive and proprietary information; 2) there is no protective order in place and there will be tricky issues to work out regarding what, if any, information in the documents Shaka should be allowed to access and what the restrictions governing the use of the documents will be; and 3) the Ninth Circuit’s ruling on the Motion to Vacate may soon moot the issue of needing those documents for the appellate record.

We realize that Shaka’s appellate brief is due on April 30, 2015, and that the Ninth Circuit may not rule on the Motion to Vacate before then. Therefore we are amenable to stipulating to extend the time to file Shaka’s appellate brief until 30 days after the Ninth Circuit rules on the Motion to Vacate. If the Ninth Circuit denies the Motion to Vacate, we can then meet and confer further about your request.

We should note that nothing in this message should be construed as conceding that Shaka has any right to access the sealed information. For example, Plaintiffs are concerned by the hostility that Shaka has shown toward the seed companies in the past and thus by the risk that it will use this confidential and sensitive information publicly for improper purposes.

Please let me know if you agree with this proposal, and we can prepare the draft protective order. If not, please let me know if there is a time tomorrow when we can meet and confer in person or by telephone about this issue.

Best Regards,
Nick


Justice? Transparency? Never heard of it.


power outside the matrix


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free emails at NoMoreFakeNews.com or OutsideTheRealityMachine.

Exposed: the Judge in the Monsanto-Maui lawsuit is tainted

by Jon Rappoport

November 26, 2014

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In a previous article, I ran down Judge Barry Kurren’s wife’s connections to big biotech in Hawaii.

Now I have more. Much more.

Judge Kurren is overseeing the Monsanto/Dow lawsuit against Maui, where the people recently voted to halt Monsanto/Dow GMO research.

Does the Judge have a conflict of interest?

Is the Pope Catholic?

Until at least the fall of 2011, Judge Kurren’s wife, Faye, was a trustee of The Nature Conservancy (TNC) (twitter), a 6-billion-dollar environmental group.

TNC specializes in working with mega-corporations, who donate major money, in return for receiving TNC’s “good housekeeping seal of approval” as friends of the environment.

It’s all very cozy.

In 2011, TNC leveraged a blockbuster deal. Dow pledged a $10 million donation. In exchange, Dow could forthwith use the TNC logo on its site and all its products.

That’s like painting a cobra’s hood with Mr. Rogers’ face.

This would be the same Dow whose GMO/pesticide experiments on Maui the voters decided to stop.

The voter stoppage provoked the lawsuit from Dow and Monsanto.

Faye’s husband Barry is the Judge in the case.

Faye was a trustee at TNC, who took $10 million from Dow.

So…what are the chances Faye’s husband will step on Dow’s face in the lawsuit?

Getting the picture?

There’s more.


power outside the matrix


TNC’s business council includes luminaries like Monsanto, Coca Cola, and of course, Dow.

Among TNC’s corporate funders: again, Dow; Coke, DuPont, Pepsi.

Could the ban-GMO movement ask for more vicious enemies?

Search the extensive TNC website and try to find one negative mention of GMOs or toxic pesticides in their “championing of the environment.”

And what about the boss at TNC?

The CEO is Mark Tercek, former managing partner at what Matt Taibbi calls the “great vampire squid wrapped around the face of humanity, relentlessly jamming its blood funnel into anything that smells like money”:

Goldman Sachs.

Tercek is also a member of the Council on Foreign Relations, the vampire squid’s brother.

Tercek writes: “We would also be smart to put more focus on making GMO technology available to lower-income farmers, given the potential benefits that climate-resilient GMO crops could bring to the developing world.”

“Climate-resilient.” Sure. What’s wrong with those damn crops that keep demanding decent weather? Fix them with new genes from Dow. Can’t wait for food that doesn’t need water or topsoil.

To repeat: Faye Kurren, Judge Kurren’s wife, was a TNC trustee.

Case closed.

Find a new Judge.

This one’s tainted.

Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free emails at NoMoreFakeNews.com.