Practice Fusion Provides Rapid EMR Response to FDA Recall of Darvocet
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Practice Fusion Provides Rapid EMR Response to FDA Recall of Darvocet
The FDA recommended removing propoxyphene (Darvon, Darvocet) on November 19, 2010 after new clinical research indicated that the painkiller can cause heart-related side effects. An estimated 10 million patients in the US are currently prescribed the common pain medication. Practice
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Tags: Pain Medication, Pain, Drug, Electronic Medical Records, FDA
Most Recently Shared on November 23, 2010 at 4:06 pm By:
Stephen Campbell - emrdailynews
Practice Fusion Provides Rapid EMR Response to FDA Recall of Darvocet http://su.pr/1F5cFG
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