A case in point: it turns out that only about half of the new prescription medications pushed onto the market over the last decade had the proper data together for the U.S. Food and Drug Administration - yet the FDA approved them anyhow.
The researchers found that only about half of 197 eligible approved NMEs between 2000 and 2010 had comparative efficacy data available at the time they were approved to be marketed.
Meanwhile, another recent study throws needed light on the limited data behind the safety and effectiveness of some Big Pharma drugs.
Health Glance
A desperate father whose son was suffering from a life-threatening brain tumour has revealed he gave him cannabis oil to ease his pain. And he has now apparently made a full recovery.
Three months after the federal government urged most Americans to sharply cut their salt intake, a new study questions whether the recommendation will benefit those without high blood pressure.
The American Academy of Pediatrics (AAP) recently issued a policy paper condemning the current Toxic Substances Control Act (TSC Act) for failing to properly regulate the tens of thousands of toxic chemicals used in various consumer products, many of which are especially dangerous to pregnant women and young children. Though correct in its identification of chemical use as a toxic threat to society's most vulnerable individuals, the AAP hypocritically continues to support the intramuscular poisoning of children through vaccinations, which are loaded with toxic chemicals that are directly injected into children's bodies.
Patients have lost access to hundreds of herbal medicines today, after European regulations came into force.
For seven years, the Food and Drug Administration has been trying to answer this question: What does it mean to be “gluten-free”? That is roughly the time it took to build a tunnel beneath the English Channel to connect Britain and France.





























