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10 Feb 2007, 9:01 pm
Food and Drug Administration (FDA) has proposed stronger warning labels on over-the-counter "painkiller" medications because of the risk of liver and stomach damage. [read post]
3 Jun 2012, 8:50 pm
Food and Drug Administration ("FDA") is warning consumers that Reumofan Plus, marketed as a natural dietary supplement for pain relief and other serious conditions, contains several active pharmaceutical ingredients not listed on the label that could be harmful. [read post]
2 Dec 2011, 9:04 am by Kay Van Wey
The popular birth control pills Yaz and Yasmin are currently being reviewed by the Food and Drug Administration (FDA) for their propensity to increase a woman's risk of having a heart attack or stroke. [read post]
21 Sep 2016, 7:41 am by Robert Kraft
The Wall Street Journal reports that Juno Therapeutics Inc. announced that the Food and Drug Administration placed a clinical hold on the Phase II clinical trial of JCAR015, an experimental leukemia treatment, because two patients died last week. [read post]
30 Jun 2012, 4:19 pm by Bryan Fears
For pregnant women and their in utero children, the risks associated with Paxil (paroxetine) are sufficiently concerning that the Food and Drug Administration (FDA) has warned patients and health care professionals that this widely prescribed antidepressant may increase the risk of birth defects in general and, in particular, heart defects. [read post]
16 Oct 2022, 5:55 am by Ilana Korchia
Food and Drug Administration (FDA) are collecting different types of data to investigate a multistate outbreak of Listeria monocytogenes infections linked to ice cream. [read post]
12 Oct 2023, 2:09 pm by Bill Marler
Food and Drug Administration (FDA), Centers for Disease Control and Prevention (CDC), and state partners conducted an outbreak investigation into a multistate outbreak of Salmonella Typhimurium linked to cantaloupe. [read post]
3 Nov 2022, 2:40 pm by Bruce Clark
According to the Food and Drug Administration, the recall was initiated on Oct. 20, and is ongoing. [read post]
18 Jul 2012, 2:59 am
Food and Drug Administration announced Tuesday that the controversial chemical bisphenol A, or BPA, can no longer be used to make baby bottles or sippy cups. [read post]
19 Oct 2011, 10:58 am by Peter N. Freiberg
Just recently, on October 18, 2011, the Food and Drug Administration issued alerts to consumers advising them not to use or purchase several products that were found to contain sibutramine. [read post]
23 Nov 2015, 12:13 pm by John S. Moffa
During the early 1990s, the company received approval for the drug from the United States Food and Drug Administration (“FDA”) for the limited purposes of treating vomiting and nausea in patients undergoing surgery and chemotherapy. [read post]
1 Dec 2013, 10:05 pm by Lydia Zuraw
Food and Drug Administration adopted a requirement that trans fats be listed on the nutrition facts panel of food packaging. [read post]
28 Feb 2012, 1:59 am
A coalition of 14 public health organizations is calling on the Food and Drug Administration to require that food labels provide full information on added sugars. [read post]
12 Feb 2015, 3:12 pm by News Desk
The company, which makes soy drinks, tofu and related products, had been cited by Food and Drug Administration officials for food safety violations several times in the past four years at its manufacturing facility in the Bayview area of San Francisco. [read post]
10 Aug 2009, 10:43 am
CDC Published this Morning: CDC is collaborating with public health officials in many states, the United States Food and Drug Administration (FDA), and the United States Department of Agriculture Food Safety and Inspection Service (FSIS) to investigate an outbreak of E. coli O157:H7 infections. [read post]
27 Apr 2012, 9:19 am by Steve Hall
There is no domestic maker of the product, and the California Department of Corrections and Rehabilitation has been ordered to turn over its foreign-bought drug to the Food and Drug Administration. [read post]
9 Aug 2018, 6:34 am by Amy Yin, Rong Mao and Liu Yang
Following the issuance of the “Opinions on Deepening the Reform of Examination and Approval System and Encouraging Innovation in the Industries of Pharmaceuticals and Medical Devices” by the Central Office of the Communist Party of China and the Office of the State Council on October 1, 2017, the former China Food and Drug Administration2* formulated and published the Amendment to the “Regulations on the Supervision and Administration of Medical… [read post]
30 Oct 2009, 2:30 pm
Food and Drug Administration today sent a warning letter to Procter & Gamble notifying the company that its Vicks DayQuil Plus Vitamin C and Vicks Nyquil Plus Vitamin C are illegally marketed combinations of drug ingredients and a dietary ingredient. [read post]