Monday, 7 December 2015

Drug Regulator tells us what drug 'side effects', and 'adverse reactions' really are

When speaking of drug side effects, ever adverse drug reactions, the terms seem quite benign - especially when mentioned by conventional doctors. So just how benign are the side effects and adverse reactions of pharmaceutical drugs?

Let's allow the conventional medical establishment have the last say in this. In particular, let's look to the world's leading drug regulator, the American Food and Drug Administration (FDA) tell us. They have a webpage entitled "Why learn about adverse drug reactions (ADR)? tucked away in the nether reaches of their website. Have a look at it, although I will copy the entire page here now.

  • Over 2 MILLION serious ADRs yearly
  • 100,000 DEATHS yearly
  • ADRs 4th leading cause of death ahead of pulmonary disease, diabetes, AIDS, pneumonia, accidents and automobile deaths
  • Ambulatory patients ADR rate—unknown
  • Nursing home patients ADR rate— 350,000 yearly

Remember, these are just figures for the USA!

Remember, these are just the numbers that the FDA are prepared to admit!

Remember that many studies have demonstrated that only about 10% of side effects and adverse reactions are ever submitted to drug regulatory agencies. So the above figures can be multiplied 10 times!

This is why I use the term "Disease Inducing Effects" or DIE's, which obviously can also mean "Death Inducing Effects" too. I have written more extensively about the harm pharmaceutical drugs elsewhere (see 'The Creation of Illness" in my ebook, 'The Failure of Conventional Medicine').

So it is satisfying that the dangerousness of pharmaceutical drugs and vaccines is recognised by the conventional medical establishment.

The problem remains that conventional doctors don't tell us about them when they prescribe drugs to us, and that the mainstream media are not prepared to investigate pharmaceutical drug dangers, and to inform us accordingly.