Re: General Discussions
Reply #1677 –
Some of you might come across some posts discussing changes to US FDA approvals on some commonly used cold and flu medicine, it seems a side-effect of many companies doing large scale trials of the efficacy of compounds in treating COVID or it's symptoms has exposed that they have components that are useless for the purpose advertised. I won't list them here, but pretty much all the big name brands have products that are affected.
To me this is a good thing, but ...............
It has exposed just another example of how weird life in the USA has become. In most cases it's a single component of those medicines that turns out to not do what it is claimed, but the medicines still have a range of efficacy delivered from the other components in the compound.
The US FDA still allows homeopathic, naturopath or pseudoscience compounds to remain sitting on the shelf, and for the packaging of those products to make outlandish claims. Like diluted 500x for maximum efficacy!
So commercial pharmaceuticals that actually do something are to be withdrawn, while the snake oil remains.
Snake Oil 1
Reality 0
This of course affects us all, because most countries globally just fall into line with basic FDA guidelines. So you might find your favourite cold and flu medicine being pulled form the shelves, but you'll still be able to purchase a jar of "500x Diluted Megatrength Devil's Ar5e Miracle Cure" so it is all good! 