I didn't say there are no risks but those risks must necessarily be very low, as otherwise with a sample size of billions of doses issued even effects in the 1 in a million would be readily identifiable.
Indeed there is no point in communicating further, you made up your mind years ago and you will probably never progress beyond repeating the old talking points. Luckily most of the rest of the world has started to see reality is a bit more nuanced than ‘COVID is doom, vaccine is good’.
it's by no means easy to identify trends that are worth pursuing for a medical investigation in a varied cohort of a billion people, and poll size is only a single attribute -- this is made even harder during a vacination campaign that is trying to effectively drive the un-vaccinated rates to as close to 0% as possible, making comparative studies even more difficult to establish.
Time/race/status/age/health all matter. You can't just take a look at what conditions that the billions of vaccinated share, that's ineffective for any kind of impact study.
It's my opinion that any 'precise' data is going to come about in years and years once we can establish a generational gap between this event and others so that we can effectively create a cross-generational comparative study.
[1]: https://jamanetwork.com/journals/jama/fullarticle/2788346
However, at the same time we have people in sibling comments claiming to know multiple people with conditions ranging from changes to their menstrual cycle to death. This can't possibly be related to the vaccine at anything like the rate people are for some reason inclined to believe.
Personally I found the effects from the 3rd booster almost as bad as COVID itself so I'm unlikely to get another unless there is a compelling reason.
What you posted was condescending and demonstrative of a large blindspot as to the degree of adverse event surveillance actually being carried out.
Hope that helps you achieve the tone of discussion you're aiming for, in the future.