Tag Archives: Thalidomide

Tromethamine Side Effects

Pfizer adds Tromethamine to the child vaccines, which is a blood acid reducer used for heart complications.

Could this be to control the heart inflammation they’re 6 times more likely to experience than their risk of Covid hospitalization?

https://www.dailyveracity.com/2021/09/09/new-studs-shows-vaccines-are-more-dangerous-to-children-than-covid/

 

https://www.drugs.com/sfx/tromethamine-side-effects.html

How do you typically react when you realize that you’ve been conned in a major way – with major long-term consequences to your life-by people you trusted?

I am asking because hundreds of millions around the world will soon find out.

Copyright Disclaimer Under Section 107 of the Copyright Act 1976, allowance is made for “fair use” for purposes such as criticism, comment, news reporting, teaching, scholarship, and research. Fair use is a use permitted by copyright statute that might otherwise be infringing. Non-profit, educational or personal use tips the balance in favor of fair use.

COVID-19 vaccines now have the highest death rate of any vaccines in history

“With over 13,000 reports to the CDC about death from the COVID-19 vaccines, COVID-19 vaccines now have the highest death rate of any vaccines in history. Indeed, the average total vaccine deaths reported each year to the CDC, before COVID-19, was a grand total of a little more than 100 a year. In other words, the COVID-19 vaccines have approximately 100 times more reports of death per year than the average reports for all other vaccines combined. In the past, individual vaccines have been taken off the market for as little as 12 to 50 reported deaths. COVID-19 vaccine deaths are catastrophic and, worst yet, reported deaths reflect only a small fraction of actual vaccine deaths in the community.

During the interview with Dr. McCullough, I occasionally fill in with information about how and why the global predators are stopping Western nations from using early treatments while pushing failed and extremely lethal vaccines.

There are few if any other interviews or sources where you can get such full and up-to-date vaccine coverage as in this presentation and discussion. ”
– Dr Peter Breggin
Watch Dr. McCullough and Dr. Breggin here.

Peter A. McCullough MD, MPH is the best source of vaccine information in the world. And this interview with me covers the most important issues: Vaccines do not protect against COVID and especially against Delta and other variants. Many hospitals have very sick COVID patients who have been fully vaccinated beforehand. Children need to get natural immunity. I believe there is good scientific justification for suggesting healthy children should have COVID parties to provide themselves the best chance of lifetime immunity to all the COVID-19 variants. Doctors and even entire nations like India that use proper early treatment such as advised by Dr. McCullough and Dr. Vladimir “Zev” Zelenko have very little problem with the Delta variant, which is now the main one in the U.S.

You can’t rush SCIENCE! #Thalidomide

Copyright Disclaimer Under Section 107 of the Copyright Act 1976, allowance is made for “fair use” for purposes such as criticism, comment, news reporting, teaching, scholarship, and research. Fair use is a use permitted by copyright statute that might otherwise be infringing. Non-profit, educational or personal use tips the balance in favor of fair use.

They will blame it on “long covid”

I think there is a possibility this drug is in the vaccines, or, they’re administering it to “covid” patients in the hospital’s.

Once the reactions and birth defects become too obvious, they will blame it on “long covid”.

Just look at the list of illnesses on the Covid19 Scenarios page. It is everything people are experiencing from the jab. But the claim will be that covid caused it.

Vaccines by definition has to PREVENT TRANSMISSION. From the mouth of the CDC director.. THEY DON”T…

Copyright Disclaimer Under Section 107 of the Copyright Act 1976, allowance is made for “fair use” for purposes such as criticism, comment, news reporting, teaching, scholarship, and research. Fair use is a use permitted by copyright statute that might otherwise be infringing. Non-profit, educational or personal use tips the balance in favor of fair use.

Trust Science By Taking Thalidomide

Source: MONERO 101

Copyright Disclaimer Under Section 107 of the Copyright Act 1976, allowance is made for “fair use” for purposes such as criticism, comment, news reporting, teaching, scholarship, and research. Fair use is a use permitted by copyright statute that might otherwise be infringing. Non-profit, educational or personal use tips the balance in favor of fair use.

Is this the worst disaster in Clinical Research (Drug)?

In the 1950s, thalidomide cut a wide swath of destruction across the world, leaving behind thousands of deformed infants, but that was only the beginning of the story.

Thalidomide – known as Contergan in Germany – is still being used as a drug. This, even after the medication caused thousands of birth defects six decades ago.

Source:

The Shadow of the Thalidomide Tragedy – NY Times

Thalidomide survivors seek justice in ‘world’s worst pharmaceutical disaster’ | Australian Story

Thalidomide: still with us half a century later | DW Documentary

Fair Use Notice: Images/logos/graphics on this page contains some copyrighted material whose use has not been authorized by the copyright owners. We believe that this not-for-profit, educational, and/or criticism or commentary use on the Web constitutes a fair use of the copyrighted material (as provided for in section 107 of the US Copyright Law).

How the Pharmaceutical Industry became into existence?

The Birth of the Pharmaceutical Industry can be traced back to 1850 – 1875 where the first “authentic” drug was developed by extracting agents from plants.

In those years, there were also developed the microbial theory of disease, medicines and homoeopathy patent and there heavy use of powerful purgatives and cathartics medicines.

By 1875, the Drug Development becomes a science and the first synthetic drug was introduced. By 1900, vaccines and antitoxins form the basis of the new pharmaceutical industry.

From 1900 to 1925, began what is now known as the pharmaceutical century. The U.S. Pure Food and Drugs Act was passed (known today as the FDA) and the development of hormonal and chemotherapy was introduced.

After 1925, it began what is known today as the Antibiotic and Regulatory Era. Vitamins, antimalarials, anticarcinogenic compounds and anti-infectives discoveries were made. The FDA gains independence as a regulatory agency and is given compliance responsibility.

From 1950 thru 1975, a new generation of the drug became apparent. Vaccines for polio became mandatory, oral contraceptives appears on the market and cardiovascular therapies.

Also, an amendment to the Federal Food Drug and Cosmetic Act of 1938 Act was signed by President Kennedy to ensure that consumers will not be the victims of unsafe and ineffective medications. Additional information about this Act can be read here: Kefauver-Harris Amendments

The Globalization of the Pharmaceuticals industry started from 1975 thru 2000. New drugs therapies, new antiviral drugs, and the development of new drugs by biotechnology companies were in global high demand.

By 2000, over 2.8 million people participated in over 50,000 clinical trials and more research and development funding was increased.

R&D Expenditures by Body System

R&D Expenditures

Cost (Billions) Body System
7.0 Central Nervous System
6.0 Cancer, endocrine and metabolic
4.5 Cardiovascular
3.5 Infectious Disease
2.5 Biological and vaccines
5.3 Other

Current Trends in the Industry since the late 2000s

Biotechnology Medicines
Drug Intervention Targets
Vaccines

 

Role of Generic Drugs
Generic drugs account for over 47% of prescription drugs in the market in which 43 major prescription drugs come off patent by 2005.

What does this mean for pharmaceutical drugs?
Between 40% – 60% of sales are lost to the generic brand within the two years of coming off patent.

Factors that will impact the R&D future:

  • There has been over 40 mergers and acquisitions since 1985
    • Sanofi and Synthelabo
    • Zeneca and Astra
    • Monsanto and Pharmacia
    • Roche and Genentech
  • Employment grew at a 3% rate per year

Total Drug Development Time (Years)

Summary:
On average, it takes at least ten years for a new medicine to complete the journey from initial discovery to the marketplace, with clinical trials alone taking six to seven years on average. The average cost to research and develop each successful drug is estimated to be $2.6 billion.

Pharmaceutical Regulation

In 1902, about 10 children die after receiving a vaccine shot. The BIOLOGICS CONTROL ACT was passed to ensure purity and safety of serums, vaccines and similar products used to prevent or treat diseases in humans.

In 1906, “The Great American Fraud” reveals patent medicines laced with addictive drugs, toxic additive and alcohol.

In 1912, Public outcry over the sales of “snake venom” and other wonder cures.  The SHERLEY AMEND was passed to prohibit labelling medicines with false therapeutic claims intended to defraud the purchaser.

In 1927, the government forms a separate law enforcement agency called the Food, Drug and Insecticide Agency.

In 1937, about 107 people, including many children die after drinking a syrup called Elixir of Sulfanilamide. Due to safety concerns, The Federal, Food, Drug and Cosmetic Act (1938) was passed as the first attempt to regulate cosmetics and medical devices.

In 1962, the sleeping pill “Thalidomide“, developed what is known today as Grunenthal Pharmaceutical in Germany, resulted in thousands of birth defects in Western Europe. The KEFAUVER-HARRIS Drug Amend was passed to ensure drug efficacy and greater drug safety.

In 1983, the ORPHAN DRUG Act was passed enabling the FDA to promote research and marketing of drugs needed for treatment of rare diseases. This year there as an outbreak of HIV / AIDS cases.

In 1988, The FOOD and DRUG ADMINISTRATION ACT were established as the FDA under the Department of Health and Human Services.

In 1992, the pharmaceutical industry complained that life-saving drugs were being reviewed too slowly by the FDA. The PRESCRIPTION DRUG USER FEE ACT (PDUFA) is made into law.

Source:

Image: Courtesy of Google image

FDA website

Private information for college researched in the 2000s.