Reglan Side Effects Lawsuit Funding
Reglan Side Effects Lawsuit Advances
Reglan (generically known as Metoclopramide), a gastroprokinetic agent and antiemetic drug, is commonly used in the treatment of nausea and vomiting.
Reglan is also used to treat nausea and vomiting in association with radiation sickness, infection, malignancy, labor, headaches and migraine, uremia and emetogenic drugs. The drug increases peristalsis of the duodenum and jejunum, increases amplitude and tone of gastric contractions, then relaxes the duodenal bulb and pyloric sphincter. These gastroprokinetic effects make Metoclopramide useful in the treatment of gastric stasis and other gastric disorders.
Reglan Side Effects
Since 2007, a lot of Reglan side effects have been discovered; these include anxiety and agitation, delirium, convulsions, increased heartbeat, fever, jitters, restlessness, loss of consciousness, with the most serious being tremors and movements that are uncontrollable in the tongue, eyes, neck or jaw. These shocking side effects caused the FDA to order the manufacturer to include a black box warning about Metoclopramide side effects.
It turns out that the longer the drug is used, the greater the likelihood will be that patients may possibly suffer adverse side effects like agranulocytosis, osteoporosis, decreased white blood cells, aldosteronism or the production of excessive hormones that may cause heart attack, heart failure, kidney failure and stroke, suicidal thoughts, depression, hallucinations, NMS or neuroleptic malignant syndrome, jaundice, neurological condition that results in death, seizures, muscle rigidity and fever, severe allergic reaction, tachycardia, tardive dyskinesia, arrhythmia with increased heart rate and involuntary movements affecting the face, limbs and body.
Tardive Dyskinesia is the most severe of the Reglan side effects. A recent study however, found another shocking discovery; a link between birth defects and Reglan use. A study about the safety of Metoclopramide during pregnancy published in mid-2009 in the New England Journal of Medicine showed that of 81,703 babies surveyed, 4,016 (4.9%) were born from the mothers who used Reglan.
In February 2009, the FDA ordered manufacturers to include a black box warning on the packaging. This warns patients that use of the drug is associated with various side effects, especially the risk of the involuntary movement disorder Tardive Dyskinesia. A black box warning is a very serious type of FDA warning, second only to an FDA product recall. Black box is the last step the FDA takes before issuing a full-fledge drug recall.
Many patients were prescribed Reglan for long-term use without knowing its full side effects, even though FDA had only approved the short-term use of Reglan. Due to the risk of adverse side effects for people who take the drug in high dosages or for prolonged periods, irreversible damage is being increasingly documented.
Reglan Lawsuit Funding
Are you currently involved in a Reglan lawsuit? If so, are you in a financial bind and need cash tomorrow? TriMark Legal Funding LLC, The Settlement Funding Company is a leading provider of pre settlement lawsuit funding and non recourse lawsuit loans throughout the United States. Call us toll-free at 1-877-932-2628 with questions or to see if you qualify.
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