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5 Jul 2011, 3:38 pm
The Rules According to the Food and Drug Administration (FDA), once drugs get their initial green-light, they can legally be prescribed for the uses indicated on the label, as well as other uses (these are known as off-label uses.) [read post]
7 Feb 2023, 10:00 pm
The US Food and Drug Administration (FDA) recently issued a notice clarifying the agency’s approach to determining the scope of orphan drug exclusivity. [read post]
7 Feb 2023, 10:00 pm
The US Food and Drug Administration (FDA) recently issued a notice clarifying the agency’s approach to determining the scope of orphan drug exclusivity. [read post]
7 Feb 2023, 10:00 pm
The US Food and Drug Administration (FDA) recently issued a notice clarifying the agency’s approach to determining the scope of orphan drug exclusivity. [read post]
7 Feb 2023, 10:00 pm
The US Food and Drug Administration (FDA) recently issued a notice clarifying the agency’s approach to determining the scope of orphan drug exclusivity. [read post]
7 Feb 2023, 10:00 pm
The US Food and Drug Administration (FDA) recently issued a notice clarifying the agency’s approach to determining the scope of orphan drug exclusivity. [read post]
7 Feb 2023, 10:00 pm
The US Food and Drug Administration (FDA) recently issued a notice clarifying the agency’s approach to determining the scope of orphan drug exclusivity. [read post]
23 Aug 2021, 5:26 am
In spite of its efforts to stop the distribution of dangerous weight loss and sexual enhancement products, the Food and Drug Administration (FDA) continues to discover weight loss and sexual enhancement products that violate the federal Food, Drug, and Cosmetic Act at various online stores. [read post]
10 Feb 2009, 10:16 pm
The FDA has authority to require a REMS under the Food and Drug Administration Amendments Act of 2007 (FDAAA) when necessary to ensure that the benefits of a drug outweigh the risks.Opioid drugs have benefit when used properly and are a necessary component of pain management for certain patients. [read post]
2 Dec 2012, 5:08 pm
The Food and Drug Administration (FDA) has hired outside advisers to investigate the drinks to determine whether or not these beverages, if consumed in excess, may cause harm or even death, especially in the young or in those consumers with pre-existing cardiac conditions. [read post]
3 Feb 2014, 8:16 am
Food and Drug Administration offers its stamp of approval on a wide range of medications and treatments each year, that green light is no guarantee that a drug won't be harmful. [read post]
10 Mar 2009, 8:46 am
Food and Drug Administration's (FDA) Center for Food Safety and Applied Nutrition (CFSAN) today issued guidance to the food industry advising manufacturers that peanuts and peanut-derived products used as food ingredients... [read post]
5 Nov 2010, 4:21 pm
Now, the US Department of Agriculture and the Food and Drug Administration are focusing on some of the best practices for growing and packing fruits and vegetables to prevent these illnesses. [read post]
26 Oct 2010, 11:27 am
The announcement comes less than a month after the Food and Drug Administration issued severe restrictions on the use of Avandia because it increased the risk of heart attacks. [read post]
12 Jul 2021, 8:26 am
The Food and Drug Administration has back-tracked on a major part of its accelerated approval of Aduhelm, a prescription medication targeted at Alzheimer’s patients. [read post]
11 Jan 2013, 3:16 am
So this news from the Food and Drug Administration may be important to the elderly: The FDA has announced that it was requiring manufacturers of popular sleeping pills like Ambien and Zolpimist to cut their recommended dosage in half for women, after laboratory studies showed that they can leave people still sleepy in the morning and at risk for accidents. [read post]
16 May 2011, 5:42 pm
According to the Food and Drug Administration (FDA), a medical food product must be formulated and processed for use in treatment of an injury (and/or other medical conditions) and be used as a treatment modality. [read post]
5 Dec 2022, 9:02 pm
The Food and Drug Administration is continuing its use of import alerts to enforce U.S. food safety regulations for food from foreign countries. [read post]
2 Mar 2012, 1:37 pm
The Food and Drug Administration (FDA) is warning consumers and healthcare providers that the use of acid reflux drugs known as proton pump inhibitors (PPI) may increase a patient’s risk of developing Clostridium difficile-associated diarrhea (CDAD). [read post]
1 May 2009, 11:54 am
"The Food and Drug Administration issued a warning today to consumers to stop using Hydroxycut because it has been linked to serious liver injuries. [read post]
