Ketamine has long been abused as a “street drug,” with side effects like convulsions, irregular heartbeat, hives, shortness of breath and blurry vision. So, why would the FDA approve a drug from this dangerous source for people who are already emotionally at risk, and put off a “natural drug” that’s safer?

Medical devices are everywhere, from tongue depressors to knee replacements to pacemakers. We’re talking about any non-drug product used in medical treatment. While it’s mandatory that companies report deaths associated with their devices, reporting any other negative outcomes is strictly voluntary.

The supplement industry is growing bigger and healthier, and Big Pharma can’t get its hands on the profits. So, along with the FDA, they are doing the next best thing for them: Holding supplements to ridiculous regulations the likes of which their deadly meds and schemes received a “pass” on…

There was a time when taking medication was pretty straightforward. Your doctor wrote a prescription, you filled it and began taking your meds. It would never have crossed your mind that there was poison in your pills. Sadly, those days are gone. Here’s more to know about the recalls…

Can you trust the ingredient panel on food packaging? I’m a doctor and I don’t. Deceptive labeling is one of the major factors behind the epidemic of chronic disease in the U.S. If you’re trying to make the right choices, here’s how to decipher their clever marketing tricks…

You wouldn’t eat food with cancer-causing chemicals in it, would you? Lucky for us, we have a government agency to warn us about such dangers. That is, when this government watchdog isn’t siding with the chemical producers, rather than with us, the consumer.