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Problem is the numbers are just from VAERS data (they are not connected to the vaccines as a cause).I get it ... the numbers/percentages.
... but I also understand that any drug with an absolute number of these adverse effects would have been pulled LONG LONG ago.
I couldn't tell from the article, but are all these adverse effects still being realized from only 5% of the lot numbers?
I don't buy the 5% lot number issue. Part of this (most of it) is there are other factors that have not been explored (demographics, regional issues, common health care systems, etc.).except for the 5% lot number thing, @JonC
hundreds of millions of jabs given ... but of 5% there is a MASSIVE massive problem.
Today you're taking a flight out of Atlanta where there are about 1000 daily departures. 50 of 'em each day will crash/burn. you gonna fly outta Atlanta?
I don't buy the 5% lot number issue. Part of this (most of it) is there are other factors that have not been explored (demographics, regional issues, common health care systems, etc.).
You suggest more time is needed to evaluate vacvines. I suggest more time is needed to evaluate potential side-effects. There just is not enough information (perhaps on both sides) to form a conclusion.
The "why not" part is the article misuses data (with VAERS).Why not?
We already know there are saline bottles in the distribution. Evidently there are varying concentrations in the distribution, too ... which would lend credence to the 5% ... which is actually pretty good. That means 95% of the vials will bring less than 5% of the adverse effects.
But I appreciate your finally accepting we didn't do NEARLY enough testing before release.
The fact there isn't a tracker listing (as less than 10% of the adverse effects get reported) for a new drug which skipped 9.25 years on the timeline ... that should be concerning, if not troublesome.
the data point about 5% lot numbers isn't in the article, it's in an analysis of the VAERS data which evidently includes the lot numbers of the cv vax vial.The "why not" part is the article misuses data (with VAERS).
This is because it is a misapplication of VAERS data.the data point about 5% lot numbers isn't in the article, it's in an analysis of the VAERS data which evidently includes the lot numbers of the cv vax vial.
You seem to disregard the compilation of the data which the government agency is reporting. How do you determine which government source to accept and which to reject?
Given this particular source says it doesn't have the full picture of adverse effects, just using the ones it DOES have is bad enough. I mean, I suppose the democrats could be dithering the VAERS data as they did the 2020 POTUS election count, but wouldn't that be just crazy conspiracy theory?
Gonna present the analogy again using the government's own statements about its data: 1000 flights each day out of Atlanta. 50 of 'em are going to crash & burn (just Atlanta, not NY, not DFW, not MIA) ... you gonna fly out of ATL? I doubt it.
I'll allow your argument about needing more data on the adverse effects aspect. If the human trials had taken the historical period of time to deploy a new TYPE of vaccine, we'd know all this; or at least we'd have a whole lot better idea than we did in Dec '20 We'd also know the necessity of boosters; the frequency and total number of 'em. But we were shocked and awed by Operation Warp Speed. We were clamoring for a "shot of hope" so we threw caution to the wind and spent hours sitting our vehicles in football stadium/NASCAR parking lots awaiting "processing."
Hmmm. Now we’re getting somewhere. One suggests more time is needed to evaluate potential side-effects. The other suggests more time is needed to evaluate potential side-effects.I don't buy the 5% lot number issue. Part of this (most of it) is there are other factors that have not been explored (demographics, regional issues, common health care systems, etc.).
You suggest more time is needed to evaluate vacvines. I suggest more time is needed to evaluate potential side-effects. There just is not enough information (perhaps on both sides) to form a conclusion.
I'm saying a connection has to be made between side-effects and the vaccine. VAERS does not do this.Hmmm. Now we’re getting somewhere. One suggests more time is needed to evaluate potential side-effects. The other suggests more time is needed to evaluate potential side-effects.
Hmmm. Now we’re getting somewhere. One suggests more time is needed to evaluate potential side-effects. The other suggests more time is needed to evaluate potential side-effects.
Yep, and also a "disconnection," if there is none. It matters both ways, and matters a lot.I'm saying a connection has to be made between side-effects and the vaccine. VAERS does not do this.
The issue is people are using VARES in a way it has never before been used and was never intended to be used.Yep, and also a "disconnection," if there is none. It matters both ways, and matters a lot.
The real question in all of this is, who cares? Or rather, who doesn't? Those who have the power, the money, and the means to investigate all of this, not to mention the responsibility, don't seem particularly interested in the truth. Not a good sign.
Good one-sided post.The issue is people are using VARES in a way it has never before been used and was never intended to be used.
Arguments using VAERS data to prove vaccine side-effects are DOA.
My point is if a trend is observed in the VAEES data this indicates studies may be necessary (depending on the possible side-effect).
I don't know if this is happening because it is so hard to get past anti-vax misinformation.
Misinformation is misinformation, regardless of the camp it comes from.Good one-sided post.
It is equally difficult to get past the the pro-mandate disinformation. Big Tech and Big Pharma are very powerful.
That's more like it. Determining where the lines are being crossed from credible to not is not a simple matter. And some very powerful people are not helping the matter, but may well be helping themselves.Misinformation is misinformation, regardless of the camp it comes from.