Summary
The FDA has proposed removing oral phenylephrine, a common ingredient in over-the-counter cold medicines like NyQuil and Sudafed, due to evidence that it is ineffective as a nasal decongestant.
The proposal follows a unanimous vote by FDA advisers last year, and recent studies showing less than 1% of the drug is absorbed into the bloodstream when taken orally.
The public comment period ends on May 7, after which the FDA may finalize the ban.
I remember like a year or two ago when they officially announced these products are LESS effective than a placebo. How the hell is it taking so long to get them off the shelves?
I assume they submitted the results and stated they need to be removed, then reviewed the supreme courts measure that stated they only have power to make measures if Congress grants them privilege to do so (precidence, set in Julyish of 2022 with the EPA) making the specialized divisions of government created by Congress illegitimate unless Congress votes on the measure afterwards, making them just superficial recommendations for Congress to wait and see what their lobbyists think is okay.
Aka will drug companies pay enough to keep us lying to the public, vs maybe we will go by the recorded data.
Exon mobile recorded their data of environmental impacts in what year? And we had battery powered vehicles traveling up to 100 miles before that time. Instead of doing what was best for the future of the people, we chose what was best for profits. Reference article for fun; https://www.corporateknights.com/transportation/half-a-century-ago-one-u-s-senator-fought-to-ban-gas-powered-cars-almost-won
Point being. what power did they have to remove them from the shelves. I assume they are launching these last ditch efforts before Biden leaves, and praying to get some support before they get chiseled away at.
Imagine where we would be if GM/Ford and such started forcing the R&D in 1975 instead of 2005, 2015 or whatever we call it now