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On April 29, 2016, the US Food and Drug Administration (“FDA”) issued the final guidance on menu labeling titled “A Labeling Guide for Restaurants and Retail Establishments Selling Away-From-Home Foods – Part II. [read post]
24 Sep 2009, 8:51 am by Jeff Lowe
Supreme Court ruling, the Food and Drug Administration has required a black box warning for the label of its generic version, promethazine. [read post]
14 Jul 2009, 6:50 pm
Food and Drug Administration has required the strongest warning label a drug can have for two painkillers, the Washington Post reported July 8. [read post]
17 Jan 2015, 10:01 pm by Dan Flynn
Food and Drug Administration (FDA) to prevent foodborne illnesses, not just react to it. [read post]
7 Oct 2022, 9:05 pm by Joe Whitworth
Food and Drug Administration, said the agency was talking about data and information every day. [read post]
12 Jul 2020, 9:01 pm by News Desk
As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its jurisdiction. [read post]
20 Jun 2010, 1:02 pm by Will Nefzger
Food and Drug Administration (FDA) announced that the Kroger Co. is recalling certain containers of Kroger Deluxe Chocalte Paradise Ice Cream because of an unlisted ingredient, tree nuts, that is potentially deadly to those allergic to them. [read post]
7 Jul 2009, 6:48 am
Melinda Beck writes in the Wall Street Journal Health Journal column, "Whether or not the Food and Drug Administration decides to limit sales of acetaminophen, consumers should know this: It's easy to take more than the recommended daily dose without realizing it. [read post]
29 Feb 2012, 7:34 am by info@thomasjhenrylaw.com
The Food and Drug Administration is warning consumers about 39 million Spinbrush electric toothbrushes that could cause severe face and mouth injuries. [read post]
19 Aug 2013, 3:14 am by Robert Kraft
The Wall Street Journal reports that the US Food and Drug Administration issued a safety alert, to warn healthcare providers and consumers that acetaminophen-based pain relievers and fever reducers, such as Tylenol (acetaminophen) have been linked to several rare but potentially fatal skin reactions, such as Stevens-Johnson syndrome. [read post]
28 Sep 2007, 6:27 pm
Report assails FDA oversight of clinical trials Federal investigator says little done to ensure patient safety WASHINGTON - The Food and Drug Administration does very little to ensure the safety of the millions of people who participate in clinical trials, a federal investigator has found. [read post]
18 Feb 2009, 8:29 am
Yesterday, the Wisconsin Supreme Court ruled that injured Wisconsin residents cannot sue the makers of defective medical devices that are previously approved by the Food and Drug Administration. [read post]
22 Aug 2012, 11:16 am
Two Congress members have urged the United States Food and Drug Administration (FDA) to revamp databases providing public information concerning the safety of medical devices that rarely are the subject of clinical trials. [read post]
22 Aug 2012, 11:16 am
Two Congress members have urged the United States Food and Drug Administration (FDA) to revamp databases providing public information concerning the safety of medical devices that rarely are the subject of clinical trials. [read post]
15 Aug 2013, 2:38 am by Robert Kraft
The Wall Street Journal reports that the US Food and Drug Administration released a statement Tuesday, detailing actions it is taking to temper the marketing of products, labeled illegally as either dietary supplements or treatments for diabetes and symptoms associated with the chronic disease. [read post]
24 Aug 2015, 7:53 am by Robert Kraft
A Federal court held that the Food and Drug Administration cannot prevent Amarin Pharma Inc. from marketing its fish-oil product for an off-label use, so long as its claims are truthful, according to a Wall Street Journal report. [read post]
18 Jun 2008, 6:05 pm
On Monday, the Food and Drug Administration posted the revised death toll on its web site. [read post]
4 Oct 2016, 10:11 am by Patrick A. Malone
A pair of academic researchers has tossed a conflict-of-interest grenade in the laps of the leaders of the federal Food and Drug Administration. [read post]
27 Oct 2010, 9:30 am by Lucas A. Ferrara, Esq.
Food and Drug Administration has approved Pradaxa capsules (dabigatran etexilate) for the prevention of stroke and blood clots in patients with abnormal heart rhythm (atrial fibrillation). [read post]