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5 May 2009, 6:00 am
As many of you may or may not be aware, on May 1, 2009 the Food and Drug Administration advised people to immediately stop using the dietary supplement Hydroxycut which is linked to serious liver injuries and death. [read post]
9 May 2011, 2:59 am
Food and Drug Administration Friday cleared the first test for Staphylococcus aureus (S. aureus) infections that can quickly discern whether the bacteria are methicillin resistant (MRSA) or methicillin susceptible (MSSA).In a news release, FDA said the KeyPath Test, manufactured by MicroPhage Inc. of Longmont, CO, takes only about five hours to identify whether bacteria in a positive blood culture sample are MRSA or MSSA, and does not require any additional… [read post]
25 Nov 2016, 10:00 pm
People who have allergies or sensitivities to peanuts run the risk of serious or life threatening allergic reaction if they consume these products, according to a recall notice posted on the Food and Drug Administration’s website. [read post]
8 Apr 2024, 6:55 am
According to the details posted online by the Food and Drugs Administration (FDA), the recall was initiated on Nov. 28, 2023, and is ongoing. [read post]
14 Mar 2009, 10:45 am
Margaret Hamburg as Commissioner of the Food and Drug Administration, and Dr. [read post]
12 Mar 2013, 7:51 am
In recent weeks, the Food and Drug Administration (FDA) has issued a number of new draft and final guidance documents on a range of issues, including financial disclosure by clinical investigators, medical device recalls, prescription drug labeling, and medical devices for pediatric uses. [read post]
30 Nov 2022, 4:01 am
On November 19, 2010, the Food and Drug Administration issued a drug recall, pulling propoxyphene off the shelves. [read post]
30 Nov 2022, 4:01 am
On November 19, 2010, the Food and Drug Administration issued a drug recall, pulling propoxyphene off the shelves. [read post]
30 Nov 2022, 4:01 am
On November 19, 2010, the Food and Drug Administration issued a drug recall, pulling propoxyphene off the shelves. [read post]
18 Oct 2012, 4:45 pm
If the products do perform as advertised, then they are considered to be drugs under the Federal Food, Drug, and Cosmetic Act. [read post]
27 Mar 2010, 2:59 am
"The sale of animals for animal-derived human food products that contain illegal levels of animal drugs poses a significant public health risk," said Dr. [read post]
29 Jul 2015, 10:02 pm
Food and Drug Administration. [read post]
22 Jun 2017, 9:59 am
The Government’s Efforts to Curb Pharmacy Errors According to an article in a recent industry publication, the Food and Drug Administration’s Division of Medication Error Prevention and Analysis (DMEPA) has recently ramped up its efforts to review drug labels prior to FDA approval in hopes of decreasing the total number of errors due to look-alike and sound-alike drugs. [read post]
30 Jan 2023, 9:14 pm
Another concern with the cancellation of the health emergencies could be the possible cancellation of the emergency declaration that has supported Food and Drug Administration’s Emergency Use Authorizations for COVID-19 testing and vaccines. [read post]
21 Sep 2016, 6:23 am
The Food and Drug Administration (FDA) recently decided to require so-called “black box warnings” on nearly 400 products, warning of the risks of combining certain opioid medications and central nervous system depressants called benzodiazepines. [read post]
24 Mar 2016, 9:25 am
“Consumers may notice that, in some cases, the pouches are bloated and product inside may have an off taste or odor,” according to the recall notice on the Food and Drug Administration’s website. [read post]
22 Aug 2017, 9:29 pm
Neither the Food and Drug Administration nor the Centers for Disease Control have disclosed potential root cause in the latest outbreak, however the factors that lead to contamination of produce are well known. [read post]
23 Feb 2007, 3:36 pm
Individuals who ordered Ambien, Xanax, Lexapro, and Ativan over the internet received a product that contained haloperidol, a powerful anti-psychotic drug. [read post]
25 Jun 2009, 8:24 am
Food and Drug Administration (FDA) advised consumers to stop use of three over-the-counter Zicam Cold Remedy products: nasal gel, nasal swabs and the discontinued “kids size” swabs. [read post]
25 Jul 2019, 9:26 am
Food and Drug Administration (“FDA”) issued joint warning letters to four companies that market flavored e-liquid (vaping) products. [read post]
