Answer:
Reglan induced tardive dysknesia is a neurological disorder caused by metoclopramide-containing drugs, i.e. Reglan.
The U.S. Food & Drug Administration (FDA) recently required the manufacturers of Reglan to add a "black box warning" to the drugs safety information warning of an increased risk of tardive dyskinesia. To read the FDA warning, please visit: http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm149533.htm.
In addition, if you or somebody you know has taken Reglan and been diagnosed with tardive dyskinesia, you should contact a lawyer asap. You may be entitled to compensation by filing a Reglan induced tardive dysknesia lawsuit.
Please visit http://www.injuryhelpnetwork.com/reglan or http://www.schmidtandclark.com/reglan to learn more about your potential for monetary recovery.