The FDA sent U.S. Marshals to seize “various animal food products” stored at a PETCO distribution center in Joliet, Illinois yesterday, because the storage conditions had been deemed unsanitary twice in a row:
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FDA: If You Use The Foot Ulcer Cream Regranex, You May Die From Cancer
By 6.7.08
Bad news from the FDA: people who treat their foot and leg ulcers with the cream Regranex are five-times more likely to die from cancer.
Drug Maker Develops "Abuse-Resistant" Oxycontin
By 5.2.08
In response to the epidemic of opiate addiction, Purdue Phrama LP the maker of Oxycontin, has developed a new version of the powerful painkiller that’s “harder to abuse.” According to an AP article, the government will soon be examining this new incarnation of the drug and evaluating the manufacturer’s lofty claims. How could this drug be made “abuse-resistant?” Details, inside…
By 4.29.08
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Food and Water Watch is suing the FDA for failure to comply with a Freedom of Information Act request to disclose the plans for how it goes about inspecting various food products. [Food and Water Watch]
FDA Report Cites 49 Safety Issues At Merck Vaccine Plant
By 4.28.08
Between November of last year and this past January, the FDA “cited 49 areas of concern, including a failure to follow good manufacturing practices” at Merck & Co. Inc’s vaccine plant in Pennsylvania. A Merck spokesman says that most of the incidents were found and reported by Merck’s own employees, and that they occurred in the manufacturing process, not the vaccines themselves: “He stressed that no contamination was found in finished vaccines and that Merck was addressing all the problems.”
Food Companies Threaten Higher Prices If FDA Increases Safety Oversight
By 4.28.08
Last week, the Grocery Manufacturers Association told lawmakers that if the FDA doubled its safety oversight budget by increasing fees from food companies, they’d have to raise prices to make up the cost. That’s right: affordable food or safe food. Choose one!
Patients Of Botched LASIK Surgery Urge FDA To Step In
By 4.25.08
Our beloved fatherteacher Ben Popken seems just fine with his newly lasered eyes, but not everyone sees such great results, says Reuters: “Blurred vision, dry eyes, glare and double-vision have led to depression and in some cases suicide, several patients told a U.S. Food and Drug Administration advisory panel.” These patients want the FDA to take a more active role in regulating the LASIK industry (currently the FDA regulates the equipment but not the people who use it).
Recalled Heparin Contaminant Confirmed, And Congress Grills FDA On Inspections
By 4.24.08
Researchers have identified the chemical in the contaminated blood thinner Heparin that killed 81 people in the U.S. and made patients here and in Europe sick:The researchers freeze-dried the heparin and used a combination of nuclear magnetic resonance imaging and liquid chromatography-mass…
Pre-Emption Doctrine Would Make FDA Responsible For All Drug Problems, Shield Big Pharma From Lawsuits
By 4.8.08
Johnson & Johnson is waiting to hear whether or not a judge in Ohio will allow any lawsuits over its Ortho birth control patch to move forward, and the New York Times says lawyers on both sides think there’s a good chance he may find in the company’s favor based on the doctrine of pre-emption. The argument goes that it’s the FDA’s responsibility to monitor the safety and labeling of drugs that go to market, and therefore if something goes wrong, it’s the agency’s fault and not the pharmaceutical company’s.
FDA Investigating Possible Increased Risk Of Suicide From Popular Asthma Drug Singulair
By 3.27.08
Concerns over “behavioral issues” with Singulair developed over the past year. Merck periodically updated the drug’s labels to include warnings for tremors, depression and anxiety. FDA spokesperson Susan Cruzan said reports of suicides by “three or four” people who were taking Singulair prompted Merck to clarify suicide warnings on labels and patient information sheets in October 2007.
Spinach Facilities Are Unsafe, Disgusting And The FDA Doesn't Care
By 3.27.08
If you like spinach you might not want to read a new report from the House Committee on Oversight and Government Reform called “FDA and Fresh Spinach Safety.”
Charges Filed Against Importers Of Toxic Toothpaste
By 3.7.08
On Tuesday, the city of Los Angeles and the FDA charged the heads of two U.S. importing companies with 14 counts each of “receiving, selling and delivering an adulterated drug,” for their roles in importing and distributing over 70,000 tubes of toothpaste containing diethylene glycol (DEG) instead of glycerin. “Each count carries a maximum penalty of one year in jail and a $1,000 fine.”
Tainted Heparin May Have Been The Work Of Counterfeiters
By 3.5.08
The U.S. Food and Drug Administration said today drug counterfeiters may have added a foreign ingredient into Chinese shipments of Baxter’s blood-thinner heparin which has been linked to 19 deaths and 800 illnesses.
Aunt Jemima Pancake Mix Recalled Mysteriously
By 3.4.08
Here’s something sort of weird. The St. Louis Post-Dispatch is saying that two products, “Aunt Jemima Complete Pancake Mix” and “Aunt Jemima Buttermilk Complete Pancake Mix” have been “recalled and are under investigation for a possible health risk, according to a press release given out by Dierbergs grocery stores.”
Claim Benefits In Airborne Class Action Lawsuit
By 3.3.08
The Airborne dietary supplement, which claims to help ward off the cold and flu, has reached a tentative settlement in a class action lawsuit that the company misrepresented its product. You can file online or by mail here. Boxes of Airborne used to cite a study by “GNG Pharmaceutical Services Inc” that said it tested 120 people and 47% showed little or no cold flu symptoms, versus 23% of a placebo. However, an ABC news investigation revealed that GNG was a two-man operation started up just to make the Airborne study, and had no clinic, scientists or doctors. Following the negative publicity, Knight-McDowell Labs removed references to the GNG study from its packages. Maybe people just weren’t reading the box carefully and failed to apply directly to the forehead.
The FDA Wants More Money
By 2.27.08
Unlike Nancy Nord (she’s the CPSC boss that tried to hint to Congress that her agency needed more funding through sly winks and interpretive dance numbers), the FDA chief is ignoring Bush’s “do not ask for more money” rule and demanding more funds.
By 2.26.08
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A new meta-analysis showed that popular anemia drugs Aranesp and Procrit increase the risk of death in cancer patients by 10 percent, a statistically significant number. [NYT]
By 2.18.08
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Time has an interesting article about the unmarked cloned beef that will be washing up at your grocery store sometime soon. Are you grossed out? Not? [Time]
