MedWatch

/Tag: MedWatch

How to Post an Adverse Event with the FDA

Pacemaker, Courtesy WikiCommons, Steven Fruitsmaak MND, August 30, 2015 ~When you have a new car that develops a “safety” issue i.e. braking, steering, airbags, wiring, engine cooling, unintended acceleration etc, the auto dealer reports the problems to the manufacturer, who by law, must report the issue to the [...]

By |2015-08-30T00:00:00+00:00August 30th, 2015|FDA News|23 Comments

FDA Asks Consumers to Report Product Failures

June 10, 2013 ~ New and Improved? The U.S. Food and Drug Administration (FDA) is celebrating 20 years of the MedWatch program by providing consumers with a new form that should encourage consumers and medical professionals to report adverse events, complications and bad outcomes with drugs and medical devices, cosmetics, [...]

By |2013-06-10T16:07:02+00:00June 10th, 2013|FDA News|4 Comments