5 ms·
Except I get to make the risk assessment for myself not someone I've never met.
by agensaequivocum 5y ago
Except I get to make the risk assessment for myself not someone I've never met.
- 28304283409234 5y agoSpoken like a true individual. Vaccines optimally work if we don't, and instead think as a community.
- s1artibartfast 5y agoSurely you must agree that there is some point where individual trumps community benefits? The hard part is deciding when. It is extremely easy to postulate hypotheticals if utilitarianism has no limitations.
- jasonhansel 5y agoLegally speaking, that isn't true (at least not in the US). Vaccine mandates (in general, regardless of today's SCOTUS decision) remain constitutional: https://en.wikipedia.org/wiki/Jacobson_v._Massachusetts https://en.wikipedia.org/wiki/Jacobson_v._Massachusetts In fact, you are perfectly within your rights to elect a state government that requires vaccination for all citizens.
- agensaequivocum 5y agoThat case is only in reference to state government not federal. No where in the constitution does the federal government receive any kind of power remotely close to that. If my state enacted a mandate, I would move immediately. While I may agree that in some cases that the state has the right to do force one, it would only be in an extremely rare, last resort, literally everyone will die case. The government should always err on the side of liberty.
- Niksko 5y agoI won't presume your qualifications, but I'll just state my opinion: the people who are qualified to perform benefit risk assessments are the people writing papers saying that the benefit risk assessment is favourable. You might be qualified to make that assessment. But you'd be in disagreement with most of your peers.
- s1artibartfast 5y agoThis statement should give you pause when the FDA has rejected the risk benefit assessments of the qualified advisory committees. https://www.nbcnews.com/news/amp/rcna2074 https://www.nbcnews.com/news/amp/rcna2074 https://www.rollcall.com/2021/11/17/fda-to-sidestep-advisers-on-boosters-for-all-approval/ https://www.rollcall.com/2021/11/17/fda-to-sidestep-advisers...
- acdha 5y agoThat was a narrow rejection based on incomplete evidence, as explained in the article. They were relying only on old U.S. data and still believed that the original 2 shots were adequate protection. This was in question at the time and subsequently there’s been a clear consensus that a booster is necessary at least until the original short timing is fixed, and, of course, that was before Omicron greatly increased the risk of exposure.
- nradov 5y agoThe original 2 shots still provide good protection. Whether that's "adequate" or not is entirely subjective and arbitrary.
- s1artibartfast 5y agoI don't think that a post-hoc justification is sufficient here. Policy makers didn't have advance knowledge that the scientific experts didn't. It may have worked out in this case, but what about the next? In particular, I am concerned about the risk assessments for the <5 population. Or perhaps the next drug\therapy. Looking abroad, you will also find cases where expert panels found questionable risk/benefit for some groups and were overruled.
- acdha 5y agoMost of what I said was available at the time (not Omicron, of course). The US agencies chose not to take non-US data seriously, similarly to when the CDC acted like Delta would magically stop at the border after it was causing huge problems in the UK & India.
- laxmin 5y agoYes sure, but you need to factor in the fact that you might be wrong and that the risk of being wrong can be disastrous for you and your family.