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> How many injections do you personally need to feel comfortable? Seven million people is way more than any clinical trial for any drug you've ever taken, and I guarantee you any of them is more likely to kill you. Again, the point is, when we observe adverse effect in the out-of-trial phase, it has hard to pin-point cause and effect. It is not a guarantee that the 7 million necessarily represent a random sample so proceeding with caution is warranted. We know, for example, vaccines have been distributed by age, and chances are, the 7 million is bias towards the older demographic. > Every single year 150 people die from taking Tylenol in the US in the normal course of treatment -- and 500 die of acute liver failure due to acetaminophen overdose. 25,000 hospital admissions. 50,000 ER visits. If we pretend that 350,000,000 people take Tylenol each year, that makes Tylenol 50% more likely to kill you than this vaccine. Again, the point isn't that {insert_your_favourite_drug} is 10x more likely to kill you - the point is, when we do not understand why something is happening, it is better to pause and detect whether there is a more fundamental issue. For example, suppose that every single injection that caused an adverse reaction was produced at the same facility and as part of the same batch - we would definitely be better off in investigating the root cause than to leave it be. Until we fully understand what mechanism is causing this adverse effect and how to best counteract it, in my opinion, a pause is warranted. |
My point is that yes, an investigation should be carried out, but stopping the trial obviously - trivially - does more harm than good due to the extenuating circumstances of the global pandemic.