Tag: Food and Drug Administration
FDA & CDC find raw pet food unpalatable
The FDA recently announced it would send field staff out to collect samples of commercially-manufactured raw dog and cat food. The samples will be analyzed for Salmonella, Listeria monocytogenes and E. coli, all of which have been found in raw pet food, in the animals who eat it, in their feces, on their bodies after eating it, in the areas they inhabit,...
Supplements are the Wild West of health. One Attorney General is out to change that.
Bold moves from the New York State attorney general’s (AG) office are shaking up the supplement industry. In February, the AG accused four retailers (GNC, Target, Walmart, and Walgreens) of selling supplements that failed to contain their labelled ingredients. Using a testing method called “DNA barcoding“, the AG’s office concluded that few of the products it tested actually contained the labelled ingredient,...
FDA and Homeopathy: Part Two.
Friends, FDA, countrymen, lend me your ears; I come to bury Homeopathy, not to praise it. The evil that homeopaths do lives after them; The good is oft interred with their bones; So let it be with Homeopathy. The noble Ullman Hath told you homeopathy was effective: If it were so, it was a grievous fault, And grievously hath Homeopathy answer’d it....
Should the FDA crack down on homeopathic “remedies”?
In the category of potentially dangerous complementary or alternative medicine, I can think of few products worse than ones claimed to relieve asthma, yet don’t actually contain any medicine. Yet these products exist and are widely sold. Just over a year ago I described what might be the most irresponsible homeopathic treatment ever: A homeopathic asthma spray. If there was ever a...
Stem cell clinics and unapproved, for-profit human experimentation
Editor’s note: I met Dr. Paul Knoepfler online in the wake of my two posts on Gordie Howe and his stem cell treatment for stroke. I was impressed by his posts on the topic and what I saw at his own blog. Given that he’s a stem cell researcher, I wanted him to write a post on stem cell clinics like the...
New FDA regulatory role threatens bogus diagnostic tests
The FDA regulates in vitro diagnostic devices (IVDs) as medical devices. IVDs analyze human samples, such as blood, saliva, tissue and urine. However, in the past, the agency did not use its authority to regulate what are known as “laboratory-developed tests” (LDTs), tests developed and performed at a single laboratory, with all samples sent to that particular lab for testing. Instead, it...
Using the fear of Ebola to promote the placebo legislation that is “right to try”
Libertarians and free market fundamentalists generally detest the FDA and want to dramatically decrease its power in the belief that the free market can guarantee the safety of drugs better than a government agency that requires strong scientific evidence of efficacy and safety before approval. Not surprisingly, they're at it again, this time in the service of promoting "right-to-try" laws and using...
The Texas Medical Board vs. Stanislaw Burzynski, 2014 edition
Here we go again. I'll give the Texas Medical Board credit for one thing. It's persistent. It's going after Stanislaw Burzynski's medical license again. Will this finally be the time the TMB puts a stop to Burzynski's abuse of the clinical trial process and patients? Or will this be a replay of the 1990s, with Burzynski slithering away yet again?
The Center for Inquiry weighs in on the FDA’s mishandling of Stanislaw Burzynski’s clinical trials
The Center for Inquiry points out how what Stanislaw Burzynski is doing corrupts the clinical trial process and harms patients.
Stanislaw Burzynski’s propaganda victory on antineoplastons: The FDA really caves
Once more, the FDA fails to shut down Stanislaw Burzynski's clinic and antineoplaston manufacturing operation. Cancer patients will suffer as a result of the FDA's failure.