FDA is infamous for 'approving' deadly drugs: Pfizer's Covid19 vaccine is one of them.

FDA approved does not mean safe.

The FDA in recent years has been approving some deadly medicines that kill people, only to later 'recall' them from the market. By the time the pharmaceutical company (makers of the deadly drug) make huge profits and FDA people get their cut through legalized quid pro quo. Making money out of people's health is nothing new for those sitting in high positions of the 'health industry'. Infact it has reached a sadistic proportions where these people enjoy it. Because now the Big Pharma is involved in eugenics and depopulation agenda. 

Still in Clinical Trails but 'Approved'.

Forget about the 'rare' drugs or drugs used in rare diseases, a common, over the counter heart burn medicine such as Ranitidine (Rantac/Zantac) was pulled off the market by the FDA because it had a carcinogenic substance called NDMA in it. It has been known to cause heart attacks, liver failure, triggering porphyria attacks and pneumonia. Imagine this drug was as commonly used as water literally. I question the conscience of the doctors who have given tens and thousands of doses of Zantac to their patients: How can you blindly believe the FDA? I remember it well when I was in medical school we were told (by seniors not by professors) not to give ranitidine for kids. But in few years I noticed Ranitidine syrups were being widely prescribed for children.

Below are 35 drugs that have been recalled from the U.S. market since the 1970s, some that had been in use since the 1930s:

1. Accutane (Isotretinoin)

2. Baycol (Cerivastatin)

3. Bextra (Valdecoxib)

4. Cylert (Pemoline)

5. Darvon & Darvocet (Propoxyphene)

6. DBI (Phenformin)

7. DES (Diethylstibestrol)

8. Duract (Bromfenac)

9. Ergamisol (Levamisole)

10. Hismanal (Astemizole)

11. Lotronex (Alosetron)

12. Meridia (Sibutramine)

13. Merital & Alival (Nomifensine)

14. Micturin (Terodiline)

15. Mylotarg (Gemtuzumab Ozogamicin)

16. Omniflox (Temafloxacin)

17. Palladone (Hydromorphone hydrochloride, extended-release)

18. Permax (Pergolide)

19. Pondimin (Fenfluramine)

20. Posicor (Mibefradil)

21. Propulsid (Cisapride)

22. PTZ & Metrazol (Pentylenetetrazol)

23. Quaalude [Marketed as: Optimal, Sopor, Parest, Somnafac, and Bi-Phetamine T] (Methaqualone)

24. Raplon (Rapacuronium)

25. Raptiva (Efalizumab)

26. Raxar (Grepafloxacin)

27. Redux (Dexfenfluramine)

28. Rezulin (Troglitazone)

29. Selacryn (Tienilic acid)

30. Seldane (Terfenadine)

31. Trasylol (Aprotinin)

32. Vioxx (Rofecoxib)

33. Xigris (Drotrecogin alfa (activated)

34. Zelmid (Zimelidine)

35. Zelnorm (Tegaserod maleate)

Source.

Think this is bad? This is just a VERY small sample.

"Ongoing recalls have gained a noteworthy amount of attention and increased concerns among healthcare providers and the patients they treat. The KHN report states that from January 2013 to October 2018, almost 8,000 medications were recalled by pharmaceutical companies across the United States and abroad."

Source.

8,000 RECALLS IN LESS THAN 6 YEARS!

"About a third of the drugs the FDA approved between 2001 and 2010 were involved in some kind of safety event after reaching the market, according to a study published Tuesday in the Journal of the American Medical Association."

Source.

"On average, about 4,500 drugs and devices are pulled from U.S. shelves each year. The recalled products have U.S. Food and Drug Administration (FDA) approval and in many cases, are widely ingested, injected, or implanted before being recalled. Although the FDA may identify concerns regarding the safety of a drug, it is the responsibility of the manufacturer to initiate and execute a recall. On the other hand, the FDA can mandate the recall of a device."

Source.

"Unsafe drugs were prescribed more than one hundred million times in the United States before being recalled."

Source.

For complete list of deadly drugs that were approved then recalled by the corrupt FDA: link 1, link 2. Imagine how many innocent people lost their lives and how many more fell sick from these medicines.

Perhaps it might be the first time that the FDA has approved a drug or biological agent which is still undergoing clinical trails. The Pfizer covid19 vaccine trails-sponsored by Pfizer and information given by Pfizer- is slated to complete by July 30, 2023. Click here for the official document.

Corporate media and corporate science have same owners: Blackrock and Vanguard. 

Even the BMJ's (British Medical Journal) Peter Doshi has raised questions upon the FDA's Pfizer vaccine approval. Click here. Moreover the 'evidence' game is quite old now. Big pharma and its arms- the CDC and the FDA (and media) know very well how to fabricate and manipulate the 'evidence' or 'data' to suit their agendas. Whenever the big pharma gets caught, they pay few billions as 'law suit settlements' which they consider as part of their investment. And business goes on as usual.

'Revolving Door':

The quid pro quo between the FDA and Big Pharma is mind boggling. The FDA directors/ commissioners and Big Pharma Chiefs interchange their posts quite often. For example FDA commissioner had resigned and joined Pfizer's board of directors in 2019. 

A 2016 study published in BMJ shows that the Journal's haematology-oncology reviewers who left the agency joined the pharmaceutical companies. Whats worse is Science magazine's investigation which discivered that 11 of the 16 medical examiners joined the pharmaceutical companies whose drugs they were recently assigned to regulate. Also consider the case of Dr. Thomas Laughren, FDA's Psychiatric wing director, left the FDA in 2012 and started a consultancy that helps the pharma companies navigate through the FDA's approval process. Click here for more 'revolving door' scandal.

A Word About FDA Chief:

Dr. Woodcock is responsible for the opiod crisis.

Meet Dr. Janet Woodcock the head of the FDA. She's the one who presided over one of the worst regulatory agency failures in U.S. history. She had a big part in America's opioid crisis including approving Opana without adequate evidence of safety or long-term efficacy, approving Zohydro despite a vote of 11-2 against approval by a scientific advisory committee, and approving promotion of OxyContin for children as young as 11 years old.

And now she approved the Pfizer V regardless that the placebo control group was given the vaccine months ago, the safety trials skipped important steps and there is no long term safety data.

More on this: Link 1, Link 2, Link 3.

Dr. Robert Malone.

Dr. Malone explains the trickery around the FDA "approval". Apparently the drug that was "approved" is not actually on the market, nor has manufacturing or labeling begun. The Pfizer product being distributed is still under Emergency Use Authorization. This matches what I saw in the documents.

Conclusion: Whether or not FDA's approval is genuine is irrelevant. Nooone has the right to force a drug or vaccine into a person's body without his consent or with force/coercion- even if its so called 'FDA approved.' Its against right to bodily integrity, right to medical freedom and against human rights. Vaccines, drugs and diet should always be a choice, not mandatory.

Also read: Why the FDA can not be trusted.