WEB Notes: “JAMA” is an “international peer-reviewed general medical journal”. They are admitting the FDA is approving of drugs that are dangerous to the public. Raise your hand if you are surprised. Yet, “experts” will tell you, hey it is “FDA complaint” so that means it is okay. Go ahead take a jab or two of the latest vaccine, the “experts” say it is safe. Yet, we see here even when they claim it is “safe” 30% is not and causes issues. In my opinion when it comes to vaccines you are better off to eat healthy. That means real food and drinks. Not fast food trash, not constant soda intake. Get some exercise and your body will be able to fend off most illness. Relying on a shot is not the answer though that is what the “experts” tell you. Actually, at some places of employment they will make you sign a paper stating as much and if you decline, well you either lose your job or wear a mask during “flu season”. Let freedom ring, let freedom ring.
Findings
Among 222 novel therapeutics approved by the FDA from 2001 through 2010, 71 (32.0%) were affected by a postmarket safety event. Postmarket safety events were more frequent among biologics, therapeutics indicated for the treatment of psychiatric disease, those receiving accelerated approval, and those with near–regulatory deadline approval.
Meaning
Postmarket safety events are common after FDA approval, highlighting the importance of continuous monitoring of the safety of novel therapeutics throughout their life cycle.
Source: JAMA Admits 30% of FDA Approved Drugs Cause “Postmarket Safety Events”