Reglan Safety Label Updates

The prescription drug Reglan is prescribed for a variety of problems that occur within the stomach or intestines. Unfortunately, it has also been linked with a host of problems. The risks of Reglan are very serious. This has led to an update of the Reglan safety label.

Black Box Warning for Reglan Use

The risks associated with Reglan use are very serious, and in some cases can be permanent and life threatening. This has led the Food and Drug Administration to order the manufacturer of the prescription drug Reglan to add a black box warning to the products safety label. The black box warning is the strongest label possible for a prescription drug. The label update warns patients and caregivers about the possible increased risk of developing life-threatening and often incurable muscle disorders after taking Reglan.

Health Risks and Reglan Use

The FDA estimates that nearly 2 million Americans take Reglan or its generic counterpart. The agency has investigated numerous reports involving patients who developed serious neurological disorders after taking the prescription drug Reglan. In the majority of cases, the adverse health effects associated with Reglan use include tardive dyskinesia, neuroleptic malignant syndrome, dystonia, and other muscle disorders.

Studies have indicated that those who take the drug for extended periods of time are most at risk of developing complications. However, they have not ruled out the possibility that short-term users may also be affected in some cases. The FDA has also found evidence that children and the elderly seem to be most at risk for complications.

Consult a Lawyer

Patients who have been affected by a neurological disorder as a result of taking the prescription drug Reglan have gone on to file lawsuits against the drug manufacturer. If you or a loved one has been harmed by the use of Reglan, you should contact a Reglan attorney to find out whether you are eligible for compensation for your injuries or hardship.