Nightmare stuff

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If there was a move to limit the drugs' availability, there would be enormous pushback from the public and the medical community.

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And there's a process for this. After a drug is marketed, the manufacturer still has to submit periodic safety reports to the FDA. This includes data from any ongoing trials and spontaneous reports received from patients and doctors.

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The FDA also monitors its own database, called FAERS, for any potential signals. Handling this sort of thing is part of my current job.

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It's time like this that I turn to my favorite author: Franz Kafka. I've found him to be quite grounding for about a decade now.

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