Tag: big pharma

FDA Orders Pfizer to Add PARALYSIS WARNING to RSV Vaccine Labels

Last Wednesday, the FDA ordered Pfizer and GSK to add Guillain-Barre Syndrome (GBS) as a serious adverse event risk warning to both Pfizer’s Abrysvo and GSK’s Arexy Respiratory Syncytial Virus (RSV) vaccine labels.

RSV is the leading cause of respiratory infection in adults over the age of 60. Prior to 2023, the CDC has not published data on the incidence of RSV death in babies and children. In 2023, the CDC estimates that approximately 100 children under the age of 5 died from RSV. Despite these low numbers, the CDC recommends that pregnant women receive an RSV vaccine to ‘protect’ their baby from RSV.

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Moderna’s only real “FDA approved” product, an RSV mRNA injection is a failure

It goes without saying that RSV is a made up “virus” and there is no need to inject anyone with any alleged vaccines for it. This will only cause damage – scroll down to the part of this article where I discuss the FDA approved labeling for these shots. Sadly some people are still in a coma missing the lessons of the past 4 years of “safe and effective” so I hope that this information will help you with your efforts to wake those people up.

Despite being fully approved by the FDA in 2024, NOT as an EUA countermeasure (as best I can determine), the total revenue for this miracle of science is $10M so far. It’s refreshing to see that most people did not fall for the bullshit of RSV. I am willing to bet that even the $10M came from obligatory purchases by HHS to “stockpile” and assassinate an occasional Native American grandma, some prisoners, or other unfortunate subjects of the government healthcare services. In other words, no real uptake is happening.

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With more Americans able to access legalized marijuana, fewer are picking up prescriptions for anti-anxiety medications – new research

In states where both medical and recreational marijuana are legal, fewer patients are filling prescriptions for medications used to treat anxiety. That is the key finding of my recent study, published in the journal JAMA Network Open.

I am an applied policy researcher who studies the economics of risky behaviors and substance use within the United States. My collaborators and I wanted to understand how medical and recreational marijuana laws and marijuana dispensary openings have affected the rate at which patients fill prescriptions for anti-anxiety medications among people who have private medical insurance.

These include:

  • Benzodiazepines, which work by increasing the level of gamma-aminobutyric acid, or GABA, a neurotransmitter that elicits a calming effect by reducing activity in the nervous system. This category includes the depressants Valium, Xanax and Ativan, among others.
  • Antipsychotics, a class of drug that addresses psychosis symptoms in a variety of ways.
  • Antidepressants, which relieve symptoms of depression by affecting neurotransmitters such as serotonin, norepinephrine and dopamine. The most well-known example of these is selective serotonin re-uptake inhibitors, or SSRIs.

We also included barbiturates, which are sedatives, and sleep medications – sometimes called “Z-drugs” – both of which are used to treat insomnia. In contrast to the other three categories, we did not estimate any policy impacts for either of these types of drugs.

We find consistent evidence that increased marijuana access is associated with reductions in benzodiazepine prescription fills. “Fills” refer to the number of prescriptions being picked up by patients, rather than the number of prescriptions doctors write. This is based on calculating the rate of individual patients who filled a prescription in a state, the average days of supply per prescription fill, and average prescription fills per patient.

Notably, we found that not all state policies led to similar changes in prescription fill patterns.

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8 Bombshell Findings In Florida’s Grand Jury Report On Big Pharma’s Covid Shots

On Tuesday, a Florida grand jury released its final report on potential “criminal or wrongful activity” regarding the creation and promotion of the Covid jabs.

Requested by Gov. Ron DeSantis, R-Fla., and authorized by the Florida Supreme Court in December 2022, the grand jury was tasked with looking into whether individuals and entities, “including, but not limited to, pharmaceutical manufacturers (and their executive officers) and other medical associations or organizations” possibly violated state law related to the development, clinical testing, and marketing of the mRNA shots. The jury previously released interim reports in February and May 2024, respectively, which undercut much of the pseudo-science pushed by government “experts” on subjects such as masking, lockdowns, and natural immunity.

Following its investigation, the grand jury ultimately declined to charge any individual or entity in the case after the jurors “did not find any statute that [they] believed would be an appropriate vehicle for a criminal indictment based on the facts” in its final report. The grand jury did, however, note that such a conclusion does not absolve entities of engaging in unethical behavior.

“We want to be abundantly clear that this does not mean we believe the actions of these sponsors were always appropriate, or that the statements they made turned out to be factually correct,” the report reads. “It just means that those actions and statements are not sufficient bases to support criminal prosecutions.”

Despite the lack of criminal charges, the jury did unearth numerous major findings in its report that shine a light on deceptive behavior and actions surrounding the development and promotion of the Covid shots. Here are some of the biggest takeaways from the analysis.

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More Big Pharma/Big Government Attacks Coming – Arepanrix: Package Insert & Approval Letter

By now, readers know this writer is a staunch advocate for proper informed consent following the informed consent process. Previously, the injectable vaccine AUDENZ for H5N1 manufactured by Seqirus was reviewed to inform the public about the product. While it was a long read, the package insert for AUDENZ proved there were not enough participants to represent the population, placebo-controlled trials were only conducted in one study, and the one-year follow-up was not long enough to uncover potential serious adverse events relating to development of autoimmune diseases. Understandably, reading package inserts is not particularly “attention-grabbing” and can be quite boring and tedious. However, it is the only way you will receive all the information you need to give proper informed consent, which includes denying taking a product. Because of the volume of data to be covered in the AREPANRIS package insert, it will be covered in two parts.

In this article, the approval letter and package insert for AREPANRIX will be reviewed. The only approval letter for AREPANRIX on the Food and Drug Administration (FDA) website is dated October 18, 2024. This letter references another letter dated April 19, 2024, which requested a supplement to their license regarding packaging to include the proprietary name of AREPANRIX. There should be another letter indicating the initial FDA approval for this vaccine. Without the initial approval letter, there is no additional information to be gleaned besides the package insert.

AREPANRIX, manufactured by GlaxoSmithKline (GSK), is approved for active immunization for the prevention of disease caused by the Influenza A virus H5N1 subtype contained the vaccine for individuals 6 months and older. AREPANRIX comes in two vials that must be mixed before administration: one contains the H5N1 antigen and the other contains the AS03 adjuvant. The AS03 adjuvant will be explained in Part II. For individuals ages 6 months through 17 years, two doses of 0.25 ml are injected intramuscularly 21 days apart. For individuals ages 18 years and older, two doses of 0.5 ml are injected intramuscularly 21 days apart. (Sections 1 through 2.2)

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2012 Whistleblower of the Year Exposed Psycho Pharma Corruption: Continues to Call for Unyielding Accountability

With the recent nomination of Robert F. Kennedy, Jr., to lead the Department of Health and Human Services, (HHS) the nation’s premier federal health agency, it’s important to remember Kennedy’s rising star began decades ago by exposing fraudulent medical/corporate research and food safety issues. In a sense, Kennedy is a kind of whistleblower on a national level.

But he’s not the only one and, with Kennedy’s rise to power, AbleChild is reminded of another whistleblower, Allen Jones, whose exposure of dirty dealing between the pharmaceutical industry and state mental health agencies needs to be remembered and recognized.

Afterall, it takes courage to stand up to corruption and Jones, not one to shy away from controversy or be strong-armed into walking away, stood up to the behemoth pharmaceutical industry and ultimately protected children in ways they will never fully understand.

In a nutshell, Jones, as an investigator with the Pennsylvania Office of the Inspector General, was tasked with investigating the State’s chief pharmacist, Steve Fiorello, who was reported to have been receiving payments from drug companies. A clear violation of Pennsylvania law. But Jones uncovered a much deeper financial scheme where the money flowing into Fiorello’s unregistered account was also flowing out of it and into an account belonging to the Director of the Texas Department of Mental Health and Mental Retardation. Jones had no idea that he was about to run head-first into the then controversial Texas Medication Algorithm Project (TMAP).

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Two undisclosed deaths in Pfizer Covid vaccine trials

Pfizer-BioNTech did not disclose the deaths of two participants in its COVID-19 vaccine clinical trials before the FDA granted emergency use authorization (EUA) in December 2020. Documents released nearly three years later revealed the deaths of a 63-year-old Kansas woman and a 58-year-old Georgia woman, both classified as “sudden cardiac death.” Researchers have criticized Pfizer for failing to report these incidents within the required 24-hour timeframe, with one case taking 37 days to be filed.

Dr. Jeyanthi Kunadhasan, an Australian anesthesiologist and researcher with the watchdog group Daily Clout, called for an investigation by Kansas Attorney General Kris Kobach. She raised concerns that withholding this information may have impacted the perception of the vaccine’s safety profile.

“If the additional two deaths had been disclosed at the time of the EUA, it would have shown that the BNT162b2 mRNA COVID vaccine intervention provided no reduction in deaths.”
— Dr. Jeyanthi Kunadhasan, Anesthesiologist, Daily Clout

These revelations are part of a broader controversy surrounding transparency. In 2022, a federal court ordered the FDA to release 1.2 million pages of clinical trial documents after rejecting a 75-year delay request. This included the trial data that Pfizer had an opportunity to disclose to the FDA’s Vaccines and Related Biological Products Advisory Committee but did not.

Kansas Attorney General Kobach has also filed a lawsuit against Pfizer, accusing the company of misleading the public about the vaccine’s safety and effectiveness. The suit alleges the company failed to disclose risks like myocarditis, pericarditis, failed pregnancies, and deaths while promoting the vaccine as “safe and effective.”

Pfizer classified the deaths as unrelated to the vaccine and omitted them from a December 2020 New England Journal of Medicine paper that lauded the vaccine’s safety and efficacy. Critics say this omission reflects a troubling pattern of selective reporting.

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Moderna Creates new mRNA Vaccine

If the aftermath of the first widespread mRNA vaccine was not enough to deter the public, the government and the Centers for Disease Control and Prevention (CDC) partnered with Moderna to create a new DNA-altering vaccination for the bird flu.

And here we go again – Moderna said that their most recent vaccine is specifically for this variant (2.3.4.4b) of the flu, which has not spread from person-to-person contact. The Science Translational Medicine published Moderna’s study of the vaccine in which they exposed ferrets to the virus. Moderna won a $176 million federal funding package back in JULY to develop this vaccination.

There are only 60 known cases of this virus among humans, and nearly everyone who contracted it was exposed to infected cattle. California has already declared a state of emergency, and every politician and pharmaceutical company that enjoyed the power grab of the first pandemic is eager for the next. I cannot fathom why anyone would take this vaccine when the last mRNA vaccination FAILED. It failed to prevent the spread or transmission of the virus and injured far more people than it helped. This is why the current investigations into COVID must remain ongoing — we cannot afford a repeat of 2020.

We seriously need MAJOR political reform. Anyone who supports the absolute immunity for the Pharmaceutical Industry should be removed from office – NOW! If one in every 10,000 General Motors cars blew up when you just turned the key but has absolute immunity from lawsuits, why fix the problem? These people know that even with normal vaccines, there is also a portion of people who will die. That is just a matter of fact. That is why they bribed our politicians for absolute immunity. Why ask for that unless you were getting sued?

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FDA Updates Recall On Blood Pressure Medication Due To Possible Carcinogen

A third blood pressure medication was recalled across the United States in the past several weeks, according to a notice updated on the U.S. Food and Drug Administration’s (FDA) website on Dec. 16.

The notice said that New Jersey-based Aurobindo Pharma USA Inc. is recalling Nebivolol tablets in 2.5 milligram doses in 30-count bottles, which are only available by prescription. Nebivolol, a type of beta blocker, is used to treat high blood pressure.

The reason for the recall is because of the “presence of nitrosamine drug substance related impurity,” adding that discovered N-nitroso nebivolol levels are above the “acceptable intake limit,” it said. N-nitroso nebivolol is a nitrosamine and is considered mutagenic.

It was first initiated by Aurobindo earlier this month. The FDA classified the recall as Class II on Dec. 16, which occurs when there is a low chance of injury or death, and a possibility of “adverse events” that may have irreversible effects. They are issued if the product can cause medically reversible or temporary health problems—or if there is a small chance of serious health consequences.

The lot numbers being recalled are: NB0224001A and NB0224001B. It has an expiration date of April 2027 and a National Drug Code, or NDC, of 59651-137-30, according to the FDA.

Nitrosamines are compounds that can increase the risk of cancer in individuals if exposed to them above levels established by the FDA, or for long periods of time, the agency says on its website.

“A person taking a drug that contains nitrosamines at-or-below the acceptable daily intake limits every day for 70 years is not expected to have an increased risk of cancer,” the FDA adds.

People who are taking medications with possible “nitrosamine impurities should not stop taking their medications” and should instead speak with a health care professional.

Nitrosamines can be found in small levels in the environment and foods, including “meat, vegetables, and dairy products,” the FDA says.

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C19 HAS TAUGHT US DOCTORS DON’T UNDERSTAND HOW MEDICINES ARE MADE

If doctors did know how medicines are made, the SARS-CoV-2 injections would never have found their way into people’s arms.

Doctors would have shouted “Nine-months to develop and make an injection? Pull the other one, matey!”

In the world of medicines, the doctor is equivalent to the pilot of an aircraft, where passenger lives are in their hands. So it is with treating disease—patient lives are in doctors’ hands.

Could you imagine a pilot allowing his aircraft to take off, knowing it had been developed and made at least ten-times faster that ever before?

The manufacturer would need to explain in great detail what it had done differently to achieve such a miraculous outcome. Questions would be:

  • How were all the component parts designed and sourced so quicky?
  • How were manufacturing and supply contracts negotiated and signed-off so quickly?
  • How much testing were the wings, engines and other safety-critical components subjected to?
  • There are lots more, feel free to insert your own questions here…

The other thing, of course, is that the physical condition of the aircraft would undoubtedly give the game away. A wonky wing maybe, the odd bump in the fuselage, wires poking out from the cockpit?

A deathtrap for all to see…

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