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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 Read more

By | 2015-08-30T00:00:00+00:00 August 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, Read more

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