These vaccines have been applied hundreds of million times in the past year, true. Therefore, we have a very good understanding of their adverse effects in the first 6-12 months. What we cannot know, however, are possible adverse effects that are longer term. Susceptibility to other diseases maybe due to a weakened immune system. Possibly a higher prevalence of autoimmune diseases.
If these vaccines were regular, inactivated virus vaccines, we could extrapolate long term effects from other similar vaccines. But this is brand new technology which affects our immune system, which is far from completely understood.
I had originally hoped that Europe’s use of AZ might have avoided the concern over new methodology. But ultimately the various problems during production, testing, and rollout, “seem” worse than the newness of mRNA (in my circles).
There are also inactivated viral vector vaccines for COVID. I got J&J because it was what was available to me. I would have gotten an mRNA vaccine if I could. I agree that the mRNA vaccines should be studied for long term effects, but with what we know about them so far, my prediction is that we will find them to be much safer in the long term than viral vector vaccines. Only time will tell.
I challenge you to try again without assumptions! Unless you are saying, for those who are unsure of long term health risks, to just follow your expectations?
Please take a pause before replying to understand why people are hesitant to blindly follow the blind
As I understand it, a reasonable comparison is between two mRNA vaccines and two flu vaccines from different years. So if you trust the 10 years of studies that don't show any long term negative effects, and you trust that the particular protein won't have long term ill effects (and, well, if it does, you'd also get them from the virus and probably worse), then the set of assumptions you need to make are relatively small, and essentially the same as the ones you'd make in getting any given flu vaccine.
So please also take the time to educate yourself before calling others "blind"!
[0]: https://www.clinicaltrialsarena.com/comment/evolution-mrna-v...
Yes! And do not forget, the limited data includes the botched 1970s flu vaccine as well. Don't forget the infamous Tuskgee experiment. These are all valid data points that people can use to say "well i'm not going to be a guinea pig until the long term data comes out". There is also data that most people don't find out they are allergic until the first shot. That's anxiety inducing!
When you start becoming empathetic to the other side, you realize that there are gaps where simply hand waving doesn't make the problem go away. And this is a problem everyone with an opinion, on this topic, seems to forget
For tuberculosis there is no approved vector based vaccine [2]. Neither for influenza [3].
[1] https://en.wikipedia.org/wiki/Viral_vector_vaccine
[2] https://en.wikipedia.org/wiki/Tuberculosis_vaccines
[3] https://en.wikipedia.org/wiki/Influenza_vaccine#Manufacturin...
My question is whether or not it is a rational position that the risk of the vaccine is higher than the risk of getting covid? Is this a conclusion that someone could reasonably come to - that they would rather have covid than be vaccinated?
If the answer to the question is no, I believe mandates from private companies are something that needs to happen as the government will not be able to act.
that is my basis. it's Smart.
What I don’t follow is that, AFAICT, full authorization is likely ~6 months from the date of filing (so November to January depending on manufacturer). So we won’t have long-term data.
Is full FDA approval meaningful to you? If so, how?
Unless you get infected, in which case you made a pretty big mistake.
So then your basically saying you don't want to get vaccinated or get covid. I'm guessing you probably also want to stop social distancing. in which case you would eventually certainly get covid if it weren't for the existence of the vaccines.
So the choices are: - Don't get vaccinated and everyone continues social distancing for several years, or until you get Covid. - Don't get vaccinated and stop social distancing once everyone else gets the vaccine - Get vaccinated
Only the third option is remotely defensible. The second option is borderline sociopathic and there are enough people taking it that it is far more dangerous than option 3.
https://www.wsj.com/articles/fda-ivermectin-covid-19-coronav...
Dr. John Cambell's video on it is worth a watch: https://youtu.be/R0-90kvoQac?t=610.
As is the ongoing meta-analysis: https://ivmmeta.com
The terrible side effects you speak of effect an absolutely miniscule number of people relative to the hundreds of millions who have had the vaccine with no such effects.
Previous to this summer I wasn't so certain that the vaccine should be effectively mandated but after seeing the effect that vaccine hesitancy has on people I know longer think there is any reason businesses shouldn't mandate their employees and customers be vaccinated.
- The pharmaceutical industry is notorious for manipulation of trial data to make their treatments looks as beneficial as possible, as they are incentivized to do so. In the current case Pfizer and others have still not made the trial data public, and probably never will [0][1]
- The main study on the Pfizer vaccine contained safety data for an average of about two months - on this basis the vaccine was declared to be extremely safe. Obviously longer term effects cannot be captured in this timeframe [2]
- Due to the requirements to generate a clear public health message, almost anything that may suggest a risk with vaccines is downplayed. See for example how VAERS data is routinely dismissed (with some reason)[3], whereas data on COVID hospitalization and death rates is largely unquestioned, despite containing some room for interpretation [4].
Again, the the totality of evidence suggests that the vaccine are safe and effective. But it is not crazy or evil, as some would suggest here, to question some of what we are being told and how the data is being presented to us.
[0] https://www.nature.com/articles/d41586-020-01911-7
[1] https://www.theguardian.com/business/2015/aug/31/pfizer-resi...
[2] https://www.nejm.org/doi/full/10.1056/nejmoa2034577
[3]https://www.reuters.com/article/factcheck-vaers-faers-idUSL2...
[4] https://www.aamc.org/news-insights/how-are-covid-19-deaths-c...
If anything, it seems like if someone doesn’t want to rely on the current EUA (because of limited data, incentives, etc.) then they shouldn’t suddenly be okay with the FDA’s full authorization.
Over the past couple years we’ve witnessed and discussed at length the level of regulatory capture that has affected the FAA (via Boeing).
That makes me wonder if the FDA has also succumbed to the same issues (via Pfizer).
The agencies have a similar role and similar potentiality for capture. Revolving doors, lots of $ at stake, huge multinational corporations.
I’ve brought this up before and was downvoted to hell. But I’m just putting it out there without bias. It’s based on a logical thought process. I don’t understand why we can’t even discuss if there are issues with the FDA’s process being corrupted by corporations with billions of dollars.
I have plenty of my own speculation, assumptions, and anecdotes, but my hope is that someone pops up with an interesting nugget of “actually, EUA < something I haven’t considered >”.
Fwiw, multiple companies mentioned they would also move to require vaccination once it’s no longer EUA. I should have included that in my original framing.
To me, that sounds more like “once the government gives us more cover, we’ll do it”. But that doesn’t tell me “who would be convinced after this milestone, but not with the current data? What changes?”.
I'm not an expert in the vaccine. So, I won't debate the details.
It is very jarring that FDA/CDC claims the vaccine is safe, but they refuse to approve the vaccine.
Unlike usual vaccine trials, these vaccines have been deployed worldwide with hundreds of millions of people across many different conditions. Europe stopped using some due to an extremely rare blood clotting episode that was tens of people out millions. That suggests that rare, acute side effects have been (mostly?) discovered.
AFAICT, the FDA rules for full licenses seem to require a six month trial, as well as more information on process / manufacturing / quality control.
That just doesn’t seem that important compared to the massive, real-world “trial” data. What am I missing?