6 ms·
This could at least be done after release, but I don’t think any incentives are there, while collecting the data is incredibly difficult
by harha 9mo ago
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_ 9mo agoIt 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_event_reporting https://en.wikipedia.org/wiki/Pharmacovigilance#Adverse_even...
- arcticbull 9mo agoThat data goes into VAERS and FAERS. You can query it in MedWatch.