Reglan

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TARDIVE DYSKINESIA LINKED TO REGLAN USE

ReglanLong term or high dosage use of Reglan (also known as metoclopramide), has been linked to a movement disorder called tardive dyskinesia, which can continue to affect Reglan users even after the drug is discontinued.

In February of 2009, the U.S. Food & Drug Administration (FDA) ordered the maker of Reglan to add a boxed warning about this risk to its label. In lawsuits filed against Wyeth, the manufacturer of Reglan, allegations have been made that Wyeth knew of a widespread tendency among physicians to mis-prescribe Reglan for long periods of time even though the medication is only approved for 12 months of use. REGLAN IS ONLY APPROVED FOR SHORT TERM USE OF PERIODS BETWEEN 4-12 WEEKS.

Click here to read the FDA Warning.

ReglanREGLAN is supposed to be prescribed as a short-term treatment for heartburn caused by gastroesophageal reflux in people who have used other medications without relief of symptoms. REGLAN is also used to treat slow gastric emptying in people with diabetes (also called diabetic gastroparesis), which can cause nausea, vomiting, heartburn, loss of appetite, and a feeling of fullness after meals.

In one study, the FDA found that about 20 percent of patients who used REGLAN, used it for longer than three months, longer than the 12 week period alloted for use of the product. The FDA also claims there were reports of TARDIVE DYSKINESIA in patients who used REGLAN (metoclopramide), and that the majority of those who reported these problems had taken the drug for more than three months.

WHAT IS TARDIVE DYSKINESIA?

Tardive Dyskinesia is horribly disabling condition that is characterized by repetitive, involuntary movements much like Parkinson's, but often times much more pronounced than Parkinsons. Even after the patient stops taking the medication, the side effects not only continue, but in many cases the symptoms actually worsened after the patient discontinued the use of REGLAN. To make matters worse, there is no treatment an no cure for TARDIVE DYSKINESIA.

  1. Were you or a loved one prescribed Reglan® or Metoclopramide?
  2. Have you or loved one been diagnosed with Tardive Dyskinesia?
  3. How long did you or your loved one take Reglan® or Metoclopramide?
  4. Did you or loved one experience any of the following symptoms?
    1. Involuntary/ repetitive movements of the extremities
    2. Facial tics
    3. Lip smacking, pursing and puckering
    4. Face Grimacing
    5. Tongue protrusion
    6. Rapid eye movements or blinking
    7. Impaired movement of the fingers.
    8. Restless Leg Syndrome (RLS)

FREE CASE REVIEW

FDA Warning for Reglan

Congress Is Considering the Medical Device Safety Act | Dallas, Texas Personal Injury Attorney Blog

By Team Member | March 23, 2009

May 12, 2009 Congress is considering a bill known as the Medical Device Safety Act to give victims back their rights to sue the manufacturers of defective medical devices. In 2008, the United States Supreme Court decided the case of Riegel v. Medtronic, which took away the rights of all consumers who were injured by…

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