Moderna completes submission for full FDA approval of vax. Pfizer seeks approval for booster dose

Moderna completes submission for full FDA approval of vax dispute the posslbie reports out of japan suspending .63 million Moderna doses over contamination.

After reports that there it had “received reports from several vaccination centres that foreign substances have been found inside unopened vials”

Which makes you ask more questions then answers.
How many of these foreign substances have already being injected in other countries and is being ignored?

Pfizer has come out into seeking approval for thier booster shot.

Moderna completes submission for full FDA approval of COVID-19 vaccine; Pfizer seeks approval for booster dose

Moderna said it has requested priority review from the FDA. The company began submitting data for its Biologics License Application, or BLA, to the FDA in June.

More Booster shots are coming for those already vaxed and no longer for the ill.
Booster shots for everyone else.


I wonder how many polticans would line up to pull more Photo ops again?

US health official recently announced the government planned to make booster doses available to fully vaccinated individuals eight months after receiving their second dose of an mRNA COVID-19 vaccine. They said booster doses would start the week of September 20, pending sign-off from the FDA and US Centers for Disease Control and Prevention.

a reply to: HawkEyi

In order to get FDA approval, they have to provide samples of the "vax" for analysis, list ALL the ingredients and demonstrate safety in the form of a lack of adverse effects including death. This should go over real well lol.

ETA: I forgot to add, they only have 14 days by law to comply.

Cheers - Dave

a reply to: bobs_uruncle

I am impressed how Pfizer managed to get go at it without providing full samples, the pushbacks in the coming months should be interesting.

originally posted by: HawkEyi
a reply to: bobs_uruncle

I am impressed how Pfizer managed to get go at it without providing full samples, the pushbacks in the coming months should be interesting.

They have 14 days to comply with the law. If they do not comply and the FDA simply rubber stamps this crap, there will be hell to pay. Pfizer wants a fall guy, the FDA and the FDA knows it. The bribes will be huge and traceable.

Cheers - Dave

They didn’t get approval

They just extended the emergency powers

Remember there is no vaccine without emergency powers

With The emergency powers gone

The vaccine wouldn’t get approved

It’s the national security state doing the vaccine pushing

So one has to ask themselves, what’s really in the vaccines

And what’s it really protecting us from?

Are they expecting a biological attack from somebody

Perhaps like China & Russia

originally posted by: bobs_uruncle
a reply to: HawkEyi

In order to get FDA approval, they have to provide samples of the "vax" for analysis, list ALL the ingredients and demonstrate safety in the form of a lack of adverse effects including death. This should go over real well lol.

ETA: I forgot to add, they only have 14 days by law to comply.

Cheers - Dave

I would have thought that Pfizer have already provided billions of samples, and that any health or certification authority are at liberty to take an actual sample that is in use and to analyze it 'six ways to Sunday'.

Also, they publish the content of the Pfizer vaccine online. This is from New Zealands' Medsafe Medicines and Medical Devices Safety Authority:

COMIRNATY™ COVID-19 VACCINE Consumer Medicine Information (CMI) summary

Moderna Inc will soon start testing its COVID-19 vaccine on pregnant women.

The Cambridge, Massachusetts-based company announced the trial on Monday, and it expected to begin on July 22.

Well, that was fast.

FDA approved which later had to be removed after all the deaths, addictions, and other side effects. Quaalude, Cylert due to liver failure, Darvon or Darvocet, Des for pregnant women which three generations later is still screwing up their health, Posicor, and Vioxx.. Look them up and even after proof see how long it took most of them to be removed from markets. But hey they were FDA approved..!

FDA approval as with most things governmental is as much about Pharma money an politics, and just maybe not so critical of an eye upon your health if big bucks are to be made by a government donor or possible future employer.. IMO

originally posted by: chr0naut

originally posted by: bobs_uruncle
a reply to: HawkEyi

In order to get FDA approval, they have to provide samples of the "vax" for analysis, list ALL the ingredients and demonstrate safety in the form of a lack of adverse effects including death. This should go over real well lol.

ETA: I forgot to add, they only have 14 days by law to comply.

Cheers - Dave

I would have thought that Pfizer have already provided billions of samples, and that any health or certification authority are at liberty to take an actual sample that is in use and to analyze it 'six ways to Sunday'.

Also, they publish the content of the Pfizer vaccine online. This is from New Zealands' Medsafe Medicines and Medical Devices Safety Authority:

COMIRNATY™ COVID-19 VACCINE Consumer Medicine Information (CMI) summary

The listings for Comirnaty are incomplete and this is a propaganda piece, it does not list all the ingredients nor does it list all the side effects, even from Pfizer's own documentation and slide presentations. This Comirnaty list is not something that would be submitted to the FDA, not the correct format or procedure.

Cheers - Dave