Reglan FDA Warning Prompt Lawsuits
Gastrointestinal products like Reglan have become big revenue generators for many different companies, as people all over the world not only suffer from these painful problems, but for many different types of gastrointestinal disorders, there is really no known cure. In recent years, several companies have produced brand-name products that were intended to be used to help manage gastrointestinal conditions.
Unfortunately, the FDA recently named the following products as potentially problematic due to their link to the development of a serious set of side effects that may prompt lawsuit action:
- Reglan Tablets
- Reglan Oral Disintegrating Tablets
- Reglan Injection
- Metoclopramide Oral Solution
Below is a brief overview of the Reglan side effects linked to these products and the steps the FDA has taken to help curtail any unnecessary developments in the future.
Reglan Side Effects Injury Tardive Dyskinesia
The side effects cannot be explained properly without first detailing the active ingredient that’s present in all of these products. That ingredient is metoclopramide, and its main function is to ramp up the speed of movement of a person’s stomach muscles, which in turn shortens the time needed to empty stomach contents into the intestines.
Unfortunately, troubling reports have recently surfaced that show that these products in question have also led to a high number of instances of a relatively rare condition known as tardive dyskinesia. This condition features symptoms that can completely debilitate a person’s ability to live a normal life, and many of them are irreversible in nature. They include, but are not necessarily limited to:
- Involuntary/ repetitive movements of the extremities
- Impaired movement of the fingers
- Tongue protrusion
- Lip smacking, pursing and puckering
- Rapid eye movements or blinking
- Grimacing
The reports used to provide the link between these products and these side effects also show that those who have used metoclopramide-containing products at a high volume for a long period of time tend to be more susceptible to the development of tardive dyskinesia.
The FDA’s StepsIn response to this issue, the FDA has taken the following steps:
- Required the manufacturers of these products to place a ‘black box warning’ on all products containing metoclopramide.
- Required the manufacturers of these products to perform a ‘REMS’ analysis, which means that they must show a clear analysis of a risk vs. reward scenario in regards to the continued use of these products.
These are two of the most severe remedies available to the FDA, and the only one more harsh in nature would be a total recall of these products. If Reglan faces massive lawsuits, this would also have an effect.
Contact a Reglan Lawyer - Class Action lawsuit
If you or someone you love has been harmed as a result of treating gastrointestinal problems with a product containing metoclopramide like Reglan, you need to act now. Contact a Reglan lawyer as soon as possible to schedule a free initial consultation and to obtain the knowledge you need regarding your legal rights and options on this Reglan lawsuit.
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- Reglan and Tardive Dyskinesia
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