So why are drugs approved in the first place?

During development, prescription drugs are designed to target a single measurable marker, such as cholesterol levels or bone density. There are thousands of such markers to target in the world of modern medicine, and if a specific drug can alter any measurable marker in a positive direction -- without killing too many people during the clinical trials -- the FDA eventually declares it to be "safe and effective" and the drug is unleashed for public consumption.

Indeed, the drug may effectively impact that one marker. But here's where the problem starts: every drug has a systemic effect, and these systemic effects are not accurately measured (or admitted) in clinical trials. For example, statin drugs do, in fact, lower bad cholesterol levels. But they do this by compromising the ability of the liver to create all types of cholesterol, including the "good" cholesterol and important hormones that the body manufactures from cholesterol. Statins may have one measurable, positive effect according to the medical charts, but they simultaneously throw off the body's healthy physiology in a hundred other ways such as blocking your sex drive.

Clinical trials don't pay much attention to these other effects; they're just looking to prove one particular thing and get FDA approval to market the drug as a miracle cholesterol fighter. What other effects the drug has on the human body are largely ignored. And when clinical trial participants start showing these severe effects, they are typically "dismissed" from the trial in order to ensure that trial results look positive. In this way, extremely toxic drugs are actually approved by the FDA as "safe."

 

 

 

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