Reglan was approved by the US Food and Drug Administration (FDA) in 1979 for short-term treatment of gastrointestinal issues. The recommended length of treatment is no longer than three months. Due to the ongoing nature of gastrointestinal disorder for numerous people, Reglan use has extended beyond the three month safety window for many—and today Reglan is considered the leading cause of tardive dyskinesia among patients with the disorder in the US.
Last year the FDA issued a black box warning for Reglan—30 years after it was approved—noting the link to tardive dyskinesia.
Women and the elderly are considered at highest risk for tardive dyskinesia. However, anyone at any age can experience the involuntary movements associated with the disorder—and for young people or those in their middle years, such a condition can affect their lifestyle, career and livelihood.
YouTube features dozens of heartbreaking videos of tardive dyskinesia patients, mostly of the elderly. However, among the videos of old men and women gumming and twitching uncontrollably are representations of young women and men at the peak of their careers exhibiting similar movements. One can imagine that an employee whose physical deportment degrades to include lip chewing or movement, tongue thrusting, excessive blinking and repetitive chewing may be in danger of losing their job. Participation in social activities is often severely curtailed as a result.
READ MORE REGLAN LEGAL NEWS
It was recently revealed that a motility agent widely used in neonatal units for premature infants was pulled from the market for safety reasons about a decade ago. The 5/3/10 issue of PR Newswire did not identify the motility agent or the reason for the safety concerns.