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25 Mar 2012, 3:07 pm
The federal government’s Food and Drug Administration (FDA) recently announced that the public should be aware of the risks associated with extended use of Actos (pioglitazone). [read post]
19 Mar 2021, 9:10 am
Find Out if You Can Bring a Zantac Lawsuit or Join a Ranitidine Class Action Lawsuit In April 2020, the Food and Drug Administration (FDA) warned that the popular heartburn medication, Zantac (ranitidine), should not be taken because of high levels of NDMA (N Nitrosodimethylamine NDMA) in Zantac medication. [read post]
25 Sep 2008, 6:07 pm
A host of Levaquin side effects is one of the reasons why the US Food and Drug Administration (FDA) has the wheels in motion for a black box warning for Levaquin. [read post]
10 May 2016, 7:31 am
Reuters reported that the Food and Drug Administration announced a Class I recall for St. [read post]
26 Feb 2020, 6:15 am
Kaiser Health News reports that a Kaiser Health News investigation that revealed the existence of a then-hidden Food and Drug Administration database filled with reports of faulty medical devices and the subsequent release of those reports have driven a raft of lawsuits and research efforts. [read post]
4 Apr 2023, 5:40 pm
NPR: The Food and Drug Administration has decided to allow some people to get a second booster with one of the COVID-19 vaccines that have been updated to target the omicron variant, NPR has learned. [read post]
31 Mar 2011, 11:45 pm
Food and Drug Administration (FDA) revealed that one sample tested positive for the bacteria. [read post]
8 Oct 2015, 7:07 am
The Los Angeles Times reports that the Food and Drug Administration said that “it was investigating reports that bronchoscopes are causing infections in patients even after the reusable devices were cleaned – the same problem seen during recent superbug outbreaks involving a gastrointestinal scope. [read post]
11 Feb 2016, 7:34 am
STAT reports that the Food and Drug Administration “said that it plans to take a far more aggressive stance in reporting on possible medical device hazards, in some cases issuing early warnings about safety risks even before those concerns have been validated. [read post]
13 Dec 2017, 6:24 am
The Washington Post reports that the Food and Drug Administration has concluded “that for carefully selected patients with profound depression, the benefits of electroconvulsive therapy…outweigh the risks of possible memory loss caused by its use. [read post]
21 Feb 2020, 6:22 am
KSNV-TV Las Vegas, reports on its website that “a recent ban by the Food and Drug Administration and the more than 2,500 reported vaping-related illnesses seem to have not deterred most young Americans in their vaping habits. [read post]
4 Aug 2021, 11:20 am
The federal Food and Drug Administration may be putting patients’ safety at serious risk by allowing medical device makers to self-police their products, notably in making crucial determinations in reporting to the agency the severity of harms the devices inflict. [read post]
1 May 2009, 11:02 am
Food and Drug Administration today issued a warning for consumers to stop using Hydroxycut products because they have been associated with liver damage, seizures, cardiovascular events, and other health problems. [read post]
1 Sep 2017, 6:54 am
CNET News reports in continuing coverage that the Food and Drug Administration “sent notice Tuesday that nearly half a million pacemakers from the health company Abbott (formerly St. [read post]
10 Sep 2024, 2:38 pm
Products that are used in the medical field on patients in the American population are monitored by the United States Food and Drug Administration or FDA. [read post]
21 Oct 2007, 5:00 am
The US Food and Drug Administration has approved the vaccination of children for bacterial meningitis. [read post]
12 Mar 2009, 3:44 am
As we discussed here, the United States Supreme Court last week ruled that state law claims for failure to include an adequate warning on a pharmaceutical label are not preempted by the federal Food and Drug Administration’s (“FDA”) prior approval of the product’s label. [read post]
19 Jan 2009, 8:57 am
The Food and Drug Administration said that salmonella was found in a package of peanut butter sandwich crackers made by Kellogg. [read post]
6 Jul 2011, 9:11 pm
Adler) Just before the holiday weekend, the Food & Drug Administration issued a new draft guidance on when dietary supplement makers must file “New Dietary Ingredient” notifications and what such notifications must require. [read post]
27 Jun 2008, 3:05 am
From the Feminist Daily News: The Food and Drug Administration denied Merck and Co Inc’s application to expand Gardasil use to women over the age of 26 on Wednesday. [read post]
