This could at least be done after release, but I don’t think any incentives are ... | Hacker News

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		harha 2 days ago \| parent \| context \| favorite \| on: Trials avoid high risk patients and underestimate ... This could at least be done after release, but I don’t think any incentives are there, while collecting the data is incredibly difficult

blackbear_ 2 days ago | [–]

It is done, in many countries there are legal requirements to report adverse events whenever they are observed upon use

https://en.wikipedia.org/wiki/Pharmacovigilance#Adverse_even...

arcticbull 2 days ago | [–]

That data goes into VAERS and FAERS. You can query it in MedWatch.

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