Speaking of people who had no business in healthcare, it did seem like a lot of the early bad reactions from the injections were nurses not injecting the stuff properly, or in the wrong place. Not that you want that poison in you at all...
From top down it was handled so poorly you'd almost think it was by design that an entire system that can handle it just decided not to for some reason.
One of the things FDA reviews (or is supposed to review) prior to clearing or approving drugs or medical devices is the risk resulting from misuse. Something which is easy to misuse or where there would be severe consequences resulting from misuse is supposed to be mitigated prior to clearance/approval.
FDA also requires (or is supposed to require) that manufacturers keep track of this post-market, so if the probability of misuse or severity of harm resulting from misuse is higher than expected, that can also trigger corrective actions (recalls and withdrawals of approval in the most severe cases).
Though of course, as we've seen, the normal rules completely went out the window for this thing. Which considering all the stupid shit I had to implement in (far less dangerous) medical devices to prevent (far less harmful) misuse kinda pisses me off.
Speaking of people who had no business in healthcare, it did seem like a lot of the early bad reactions from the injections were nurses not injecting the stuff properly, or in the wrong place. Not that you want that poison in you at all...
From top down it was handled so poorly you'd almost think it was by design that an entire system that can handle it just decided not to for some reason.
One of the things FDA reviews (or is supposed to review) prior to clearing or approving drugs or medical devices is the risk resulting from misuse. Something which is easy to misuse or where there would be severe consequences resulting from misuse is supposed to be mitigated prior to clearance/approval.
FDA also requires (or is supposed to require) that manufacturers keep track of this post-market, so if the probability of misuse or severity of harm resulting from misuse is higher than expected, that can also trigger corrective actions (recalls and withdrawals of approval in the most severe cases).
Though of course, as we've seen, the normal rules completely went out the window for this thing. Which considering all the stupid shit I had to implement in (far less dangerous) medical devices to prevent (far less harmful) misuse kinda pisses me off.