by Catherine J. Frompovich A most important FDA file somehow was emailed to me and, as a consumer health researcher, retired healthcare professional, consumer health author/journalist/blogger, and certified paralegal, after reading it, I feel it is my moral duty to share it with all citizens…
By Heather Callaghan Raw milk has been featured in two different recent comedy shows… The characters on popular comedy show, Portlandia, recently experienced pure ecstasy while imbibing unpasteurized milk. They could just swear they were smarter, more fit and more fluid after milking cows and…
Natural Blaze Elderly people twice as likely as middle-aged to be given these drugs despite greater risk of side effects Less than half of UK prescriptions for antipsychotic drugs are being issued to treat the serious mental illnesses for which they are mainly licensed, reveals…
by Norma Erickson Malfeasance is when a public official violates the public trust by performing an act that is wrongful, legally unjustified, or contrary to law. Nonfeasance is the failure to act where there is a duty to act. Misfeasance is conduct that is lawful…
By Daisy Luther, The Organic Prepper Well, our good friends at the FDA are looking out for us again. Thank goodness we have them to fine us, charges us fees, regulate perfectly natural things, and keep us safe. Heck, who knew that women couldn’t even…
Carey Wedler, TheAntiMedia November 25 2014 – Last Thursday, the Food and Drug Administration approved a new painkiller that claims to combat the nation’s widespread, lethal addiction to painkillers. In 2010, anywhere from half to three-quarters of drug overdoses in America were from painkillers. 12 million people abused…
By Lisa Bloomquist, Collective-Evolution “A few popular antibiotics affect DNA, similar to some chemotherapy agents. If you’re sensitive to them, you could pay a neurological price that causes sudden and serious neuropathy and degrees of brain damage. The Food and Drug Administration is concerned about…
Information is lacking on most implanted medical devices cleared by the U.S. Food and Drug Administration despite a legal requirement that companies submit scientific evidence about the devices’ substantial equivalence to other devices already on the market. Under what is known as the 510(k) review,…
New study compared warning and withdrawal rates for drugs released before and after the drug industry increased funding to the FDA to expedite drug approvals What’s safer: a newly approved drug or one that has been on the market much longer? Newer drugs have a…
University physician calls on FDA to address hidden risk The agency charged to protect patients from dangerous drug side effects needs to be far more vigilant when it comes to medications that affect blood pressure. Robert P. Blankfield, MD, MS, a clinical professor of family…
By Heather Callaghan Just like its five previously approved counterparts, advantame is said by the FDA to be low-calorie and doesn’t generally raise blood sugar. The FDA gave the green light to the new artificial sweetener on Monday. It is a white crystalline that dissolves…
