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harhalast Tuesday at 12:51 AM2 repliesview on HN

This could at least be done after release, but I don’t think any incentives are there, while collecting the data is incredibly difficult


Replies

blackbear_last Tuesday at 9:12 AM

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...

arcticbulllast Tuesday at 1:57 PM

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