Thursday, December 08, 2016

Using Adverse Event Reports to Monitor Cosmetic Safety

Center for Food Safety and Applied Nutrition

Using Adverse Event Reports to Monitor Cosmetic Safety

December 8, 2016

It’s not an exaggeration to say that everyone uses cosmetics, be it shampoo, mouthwash, a moisturizer or deodorant. The FDA monitors cosmetics on the market to ensure that they are safe for consumers.

One way in which FDA finds out about a safety issue is when an adverse event report (AER) is filed by a consumer, manufacturer, or health care professional. An adverse event could be any problem experienced when using a cosmetic product. On Tuesday, Dec. 6, 2016, FDA announced that it is making public certain data that the agency’s Center for Food Safety and Applied Nutrition (CFSAN) receives about adverse events associated with the use of its regulated products, which include cosmetics.

Why FDA Is Making Data Extracted from Reports of Adverse Events for Foods and Cosmetics Available to the Public

A Brighter Outlook Could Translate To A Longer Life

http://www.npr.org/sections/health-shots/2016/12/07/504709736/a-brighter-outlook-could-translate-to-a-longer-life

Thursday, November 10, 2016

Vitamin D Eases Depression, Fatigue in Spinal Cord Patients

For patients with spinal cord injury who have insufficient levels of vitamin D, supplements can improve symptoms of depression and fatigue, according to a report presented to the American Academy of Physical Medicine and Rehabilitation 2016 Annual Assembly.

And in these patients, pain severity scores were significantly better with high-dose supplements than with low-dose supplements.

"We need to screen everyone with spinal cord injury for vitamin D," said the lead author.

In the study, all patients had levels of 25-hydroxyvitamin D were below 30, even those that hailed from "sunny California".

Patients randomly allocated to the low-dose group received 800 IU of vitamin D daily for 6 months. Those randomly assigned to the high-dose group received 2000 IU daily for 6 months if their baseline blood levels were 20 to 30. They received 4000 IU daily for 1 month and 2000 IU daily for 5 months if their baseline blood levels were lower than 20.

During the study period, all patients experienced a significant increase in average 25-hydroxyvitamin D levels. High-dose supplementation was associated with a significant decrease in depression and fatigue.

Study Calls Into Question Sunscreen in Melanoma Prevention

http://www.medscape.com/viewarticle/871438