Pfizer applied for Emergency Use Authorization for their Covid-19 vaccine immediately upon completing the trials successfully. Great Britain’s health organization met immediately and approved it for use. People in Great Britain started receiving the vaccine. Even Bahrain embraced it.
Not here, though. Despite the fact the President had authorized millions of doses to be manufactured in advance, and ready the second the drug was approved–and tasked a General to handle logistics and distribution–the United States did not launch quickly.
Why? The FDA. Despite the urgency of getting the vaccine out–with the whole world waiting for it, and the threat of more Americans becoming infected and possibly dying, the FDA set their hearing almost three weeks after the application was made.
Geez, I hope this didn’t interrupt your golf game, FDA!! They were in no rush. They set a December hearing, held it, and then waited another two days to approve it.
And that is how you know you have been conned.
Is the virus real? Yes. Is it deadly? For some, yes. For those who are very sick, are the therapeutics essential? You bet. For those who are afraid of getting it, whose lives have turned into a virtual house arrest, should the vaccine arrive “yesterday,” as the saying goes? Yes.
If our officials were truly concerned about all the “news” about rising infections and the spread of new cases–and the ensuing percentage of deaths that could occur each day the virus is spreading–why would they not hold their hearing immediately, even in the middle of the night if necessary? After all, by their logic, each day that goes by, more people are getting this virus. And if more people are getting it, more people will die, right? So, why would you wait even one day to authorize the release of a preventative vaccine? Why would you risk even one more American life?
After all, we have been told and told and told and told that we have to stay locked down until a vaccine arrives. We have been told we are killers to even want to try to work, or save our businesses, or even take a walk–that we must shrink and restrain ourselves from all normal activities until the vaccine arrives.
So, why the three week delay in even reviewing the request? Is it that they don’t care that more Americans in that three weeks would be exposed to and contract the disease, possibly die from it? Are those unsuspecting Americans unimportant? How many did contract it from Nov. 20-Dec.11?
Apparently this virus is not really that great a concern to them. It’s the lack of sense of urgency at the FDA that tells you, you have been conned! It is a real threat, but not one that should have stopped you cold for 10 months. The President and his team moved heaven and earth to get a vaccine created, only to have a mysterious hold interposed. Friends, if they had started the review on Nov. 20 when the request first came in–after all it wasn’t like the whole world hasn’t been waiting for this, and they knew it was coming–and if the review took 20 days, we might accept it as “procedural” and “cautionary.” But to not even start the review until Dec. 9 is a glaring oddity.
Either this virus is not as threatening as you have been led to believe, or our FDA is incompetent and tone deaf. If this is a reflection of their “professionalism,” I certainly don’t want any form of government control of my health care.
Someone took this virus and used it for other purposes, for other agendas. And the sooner, my friends, you realize that, the better. As the saying goes–Fool me once, shame on you. Fool me twice, shame on me.
It is interesting how the actual people responsible manage to hide behind the acronyms (ie FDA, CDC etc. Perhaps their names should be made known and some finger pointing done.