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13 Nov 2009, 5:00 am by Michael O'Connor & Associates, LLC
Food and Drug Administration announced that labels for Byetta, an injectable, blood-sugar-lowering drug used to treat type 2 diabetes, would be updated to warn those taking the drug of an increased risk for kidney problems, including kidney failure. [read post]
17 Oct 2011, 6:17 pm
Two webinars scheduled early next month will help members of the Grocery Manufacters Association adjust to "the rapidly changing landscape of food safety law" and a proposed rule affecting nutrition facts labels that is expected soon from the Food and Drug Administration (FDA).Starting at 1p.m. [read post]
2 Mar 2011, 2:04 am by Bob Kraft
Medscape reported, “The US Food and Drug Administration (FDA) has issued a Class I recall for certain lots of implantable infusion pumps manufactured by Medtronic, which are used in patients undergoing therapy that requires the constant delivery of drugs or fluids. [read post]
2 Feb 2011, 4:04 am
According to the Food and Drug Administration (FDA) after conducting an inspection at Dairy Farmers of America in Minnesota, FDA investigators documented serious violations of the Current Good Manufacturing Practice regulations for foods, Title 21, Code of Federal Regulations (21 CFR), Part 110 Current Good Manufacturing Practice in Manufacturing, Packing, or Holding Human Food (CGMP) regulations. [read post]
30 Sep 2010, 12:08 pm
  According to the AP, the Senate will consider a food safety bill (S. 510) after the November elections that would give the Food and Drug Administration more power to prevent foodborne illness. [read post]
8 Aug 2024, 5:55 am by News Desk
According to the details posted online by the Food and Drugs Administration (FDA), the recall was initiated on July 22, 2024 and is ongoing. [read post]
10 Jan 2011, 12:20 pm by Steve Hall
Food and Drug Administration, which certifies domestic supplies of sodium thiopental for medical use, says it approves the importing of drugs for lethal injections without examining their contents.Because its mission is "protecting the public health," the agency said Thursday, it "chooses to continue to defer to law enforcement on all matters involving lethal injection. [read post]
24 Oct 2018, 9:03 pm by Joe Whitworth
The study, supported by the United States Food and Drug Administration, found some costs could be avoided through practical and often low-cost behavior and infrastructure changes at points along food value chains. [read post]
20 Jun 2013, 2:28 pm by Mark Zamora
But it also contains sibutramine, a prescription diet drug that was so dangerous it’s been pulled off the U.S. market, the Food and Drug Administration says.The FDA issued warnings about a batch of similar slimming products – all claiming to be natural, and all containing not only sibutramine, but phenolphthalein, a laxative that’s also been pulled out of pills because it might cause… [read post]
2 Oct 2017, 10:35 am by Anthony Marangon
The Food and Drug Administration knows the names and locations of supermarkets and other retailers which sold Maradol papayas that are contaminated with Salmonella and that are the subject of a nationwide recall. [read post]
7 Sep 2010, 8:05 am
"  Recently, the criminal division of the Food and Drug Administration (FDA) and the Justice Department joined the investigation of the Iowa egg operations. [read post]
8 Jan 2016, 4:10 pm by Sabrina I. Pacifici
Specifically, drugs compounded for animals can serve as treatment options when no suitable drug approved by the Food and Drug Administration (FDA) is available. [read post]
11 Aug 2022, 7:35 pm by Josh Fensterbush
Food and Drug Administration (“FDA”) the Company is expanding its July 28, 2022, voluntary recall of nutritional and beverage products to include additional brands and code dates. [read post]
21 Mar 2022, 9:49 pm by Bill Marler
Food and Drug Administration released findings from a sampling assignment that collected and tested processed avocado and guacamole from November 2017 to September 2019. [read post]
21 May 2019, 12:40 pm by Tom Lamb
Following Health Canada’s request, [Hoffmann-La Roche Limited] performed a cumulative, comprehensive assessment of serious hepatic injury including hepatic failure reported with ACTEMRA across all available clinical and post-marketing data sources, including data from the Food and Drug Administration Adverse Event Reporting System (FAERS) and Eudravigilance (EV) databases and from the literature. [read post]
26 Jun 2007, 3:48 am
"India and China, countries where the Food and Drug Administration rarely conducts quality-control inspections, have become major suppliers of low-cost drugs and drug ingredients to American consumers. [read post]
11 Nov 2008, 5:37 pm
Food and Drug Administration informed health care professionals that the agency was investigating a report of a possible association between the use of Vytorin and an increased risk of a variety of cancers. [read post]
29 Apr 2010, 7:14 am by Oklahoma City Attorney
  Initially, the drug was subject to warnings of these Avandia side effects after GlaxoSmithKline, the manufacturer of Avandia received prompting from the United States Food and Drug Administration (FDA). [read post]
5 Aug 2009, 1:19 pm
According to the Food and Drug Administration (FDA), the agency will require drug manufacturers who produce so-called TNF blocking medicines to revise their labeling to reflect the increased cancer risk. [read post]