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by jeremyarussell
5149 days ago
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I don't see how the example you list is relevant to my argument that with proper disclosure and warning of risks people won't be able to decide if the risks out-way the gains. Example I listed: That with full disclosure I can make an educated choice as to what goes into my body. Example you listed: That over 50% of people that get prescribed something decide to take that something the wrong way as opposed to as directed. They don't seem to be the same. (for one, using a drug in a matter different then what you've been told to is just gross negligence.) |
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My argument is this: If you can't count on people to take a drug that will drastically reduce their likelihood of dying, how can you trust them to accurately determine the trade-off between efficacy and safety?
Most patients don't display the ability to figure out risks and trade-offs now (and relatively simple trade-offs at that). Do you think they'll be able to figure out what "45% increase in the risk of heart-attacks (41.2 - 48.8%, 95% confidence interval) in populations who have had a transient ischemic attack in the last 180 days, excluding those who have diagnosed atherosclerosis" means to them?