Use of the gastrointestinal drug
Reglan, and other generic drugs containing Metoclopramide, can cause a
disabling neurological syndrome known as Reglan tardive dyskinesia, which involves involuntary and repetitive movements that can be
permanent. These Reglan neurological problems are devastating and socially disabling,
causing severe physical, mental, social and emotional suffering. In February 2009, the
U.S. Food & Drug Administration (FDA) mandated that the makers of Reglan
add a black box warning to its label regarding the risk of tardive dyskinesia
associated with chronic, long-term use. The FDA’s mandate followed the
publication of analyses that suggested that Reglan is the most common cause of
drug-induced movement disorders.
To prevent tardive dyskinesia and other Reglan side effects, the drug should not be taken for
more than 12 months, and it has not been approved for longer user. However, it
has become