Corruption at the FDA is to blame for the dramatic increase in drugs adverse events, deaths

Wednesday, January 18, 2017
By Paul Martin

by: JD Heyes
NaturalNews.com
Wednesday, January 18, 2017

A Trump presidency may very well usher in the kind of health choice and health freedom tens of millions of Americans have been waiting for, given statements he made during his first press conference recently about seriously reforming Big Pharma.

Any reforms that Trump will enact seriously could not come soon enough. And with it, here’s hoping that those reforms also extend to the federal agency that ostensibly oversees Big Pharma: The Food and Drug Administration.

As reported by the trademarked Pharma Marketing Blog, some 128,000 hospitalized patients die every year from ADRs—Adverse Drug Reactions—and Adverse Events. That matches stroke as the fourth leading cause of hospital deaths, as noted here. Death from health supplements, which the FDA refuses to back despite scores of clinical studies demonstrating their benefits, don’t kill anyone.

Deaths and serious reactions outside of hospitals due to Big Pharma ADRs dramatically increases the overall death rates. And that also doesn’t include deaths and hospitalizations from overdosing patients, medication errors, and recreational drug use [RELATED: Check out the latest figures at PharmaDeathClock.com].

All of this is made clear via the hundreds of thousands of drug “Adverse Event Reports” (AERs) that the FDA receives each and every year coming directly from healthcare providers including physicians, pharmacists, nurse practitioners, physician assistants, nursing staff and others. Also, consumers and drug companies also send AERs to the FDA, the latter being a required reporter of adverse effects.

The Rest…HERE

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