Considering not everyone who gets infected gets symptoms, would it be illogical to not take the vaccine, just in case you get infected and get symptoms, but to take the drug once you do get infected and get symptoms?
To determine if this is a rational strategy or not, we'd have to get real numbers (is it really likely that 1 in 100k people die from taking the vaccine?), and compare that against the reduction in probability of dying from COVID by even combining both treatments.
And please, I just made up these numbers to answer the posed question:
> how can "I'll take experimental treatment B instead of experimental treatment A" be an argument
The numbers could lean either way and would be very sensitive to variations in the probabilities involved - I'm sure it would be very hard to reach any form of consensus on "probability of dying from taking the vaccine". It's also worth addressing wasn't even making the point of which (so-called) experimental treatment has a better likely outcome but rather addressing criticism at (so-called) experimental treatments in general.
From an "unknown risk" perspective, you'd also have to consider that COVID itself could have yet-unknown long-term risks.
That would not factor into a correct analysis: the unknown risks of covid are the same whether or not you get vaccinated (or any other treatment) because by definition the vaccine has not been shown to mitigate the unknown risks.
Same can be said for any patented-molecule treatment. But that's just a new type of molecule, not a whole other type of treatment. Hence I'd say that molecule-drugs are less experimental than mRNA-vaccine jabs.
I'd argue that mRNA vaccine development represents the most rigorous that the field of vaccinology has ever been, but those (Adenovirus) vaccines use a well tested, not-previously-experimental delivery technology. Do you have an objection to them?
Also, mRNA is not the only type of vaccine for COVID.
Finally, two more questions: would you clarify which definition of "experimental" you subscribe to? And do you have a source for "testing standards were reduced"?
https://languagelog.ldc.upenn.edu/nll/?p=50886
> Also, mRNA is not the only type of vaccine for COVID.
I know.
> Which definition of "vaccine" do you subscribe to that these "treatments" don't fit into?
It's all marketing at this point. mRNA-treatment does not sell. Vaccine elicits people's trust, and obedience.
> would you clarify which definition of "experimental" you subscribe to?
Not FDA approved in the US. "approval pending"
> And do you have a source for "testing standards were reduced"?
These kind of drugs take years to develop. This stuff was done in a few months. They skipped some steps in the process. Understandable, but still...
Here's a link to the Wikipedia entry from 2017, same text: https://en.wikipedia.org/w/index.php?title=Vaccine&oldid=798...
Here's a link to the CDC definition from 2017: https://web.archive.org/web/20171203162427/https://www.cdc.g... ("Vaccine: A product that stimulates a person’s immune system to produce immunity to a specific disease, protecting the person from that disease.")
> It's all marketing at this point.
Definitions made prior to the pandemic would already fit the mRNA vaccines, therefore the claim that the definition was stretched for marketing/persuasion reasons don't really hold water.
> Not FDA approved in the US. "approval pending"
This FDA link claims Cominarty was approved in August 23 2021. The word "pending" is not found in this page.
https://www.fda.gov/news-events/press-announcements/fda-appr...
> These kind of drugs take years to develop. This stuff was done in a few months.
"The first human clinical trials using an mRNA vaccine against an infectious agent (rabies) began in 2013." (from https://en.wikipedia.org/wiki/MRNA_vaccine)
Of course the actual individual version for COVID-19 is newer, but then again, so is any flu vaccine that is updated basically yearly. What matters is the age of the "vaccine platform".
> They skipped some steps in the process.
Citation needed?
> Definitions made prior to the pandemic would already fit the mRNA vaccines, therefore the claim that the definition was stretched for marketing/persuasion reasons don't really hold water.
You you say mRNA treatment is not new? I think this is the first rollout of such medicine on humans.
> "Approval pending" / "Citation needed? "
Ok, I misquoted this. Here what I did mean:
https://en.wikipedia.org/wiki/History_of_COVID-19_vaccine_de...
See the PhaseIII trails were allowed to be skipped with the EUA.
The process by which the treatment is now pushed to kids is even more botched.
I believe we are exposing the younger (say <60) to risks bigger than the c19 poses itself. Yes we're dealing with an overly stressed healthcare system, but that's a different matter. The jab should be worth it for the person him/her self, and that should be made clear to that person, if they dont believe it they will not take it and that's their choice.
Im okay with tax being used to give people that want the free jabs. Im not okay with persuding people to to take it with anythign other than data.