Monthly Archives: May 2012
Defective medical devices and pharmaceuticals are everywhere it seems.
These defective devices include any apparatus, machine or implant that’s utilized to enhance your overall well being. They are the ones that fail to work correctly which then results in patient injury and worse, death.
Most of defective medical devices are normally products like pacemakers and defibrillators. These devices fail because of inappropriate design or harm a patient because the maker’s negligence. Nevertheless, devices like x-ray machines, including diagnostic equipment can also be defective and can cause injuries among patients.
What Makes Defective Devices to be Defective?
Most of the injuries caused with defective medical devices are because of the negligence of the manufacturer. Every so often, manufacturers are so eager to get approval from the FDA to gain profits right away without even understanding how their devices might do if they don’t have necessary research or suitable pre-clinical tests withy those devices.
A medical devices recall doesn’t mean that the device must be removed or discontinued in usage. This only means that the apparatus needs to be adjusted or checked. If it’s found that your implanted device fails, you must talk about with your doctor the threats of having it removed against the risk of potential malfunction.
Budget reductions are one of the reasons why the product is being recalled. Necessary testing has no room for the accuracy of the device if the financial support for research and development is cut. A design defect may also arise throughout the drug’s planning procedure, and possibly will not be covered until the medicine has been widely distributed.
What are the Reasons for a Product Recall?
There are several reasons for a product recall. First off, a device needs to be fixed. The defective device has a huge defect and needs to be destroyed. It could also include the patients being checked for heath risks connected with the product. The settings of defective device need to be adjusted. The product recall occurs when the device must have its inspection. Also, new labels or warnings are required for certain device.
Companies that produce medical devices have a responsibility to give safe and dependable products that function as what it should be. Even as a medical device functions as intended, there are further risks that should be exposed. The law calls for product makers to disclose any recognized problems regarding the side effects, failures or additional potential issues related with the apparatus.
Common Defective Devices
There are several of medical services that contain defects. These devices include dialysis machines, defibrillators, stents, and pain pumps. Spinal discs, prosthetics, joint replacements parts, diagnostic equipment and heart valves also joined the long list
Who Should Be Held Responsible for Pharmaceutical Negligence?
Manufacturers are usually the ones who are held legally and financially accountable for injuries sustained from the use of defective or faulty drugs and pharmaceuticals. Sometimes however, wholesalers and distributors, including marketing companies can also be held legally responsible. And finally, doctors, hospitals and other healthcare facilities can be held liable as well, particularly if the drug or pharmaceutical was prescribed for a purpose beyond the scope of it’s FDA approval, without regard to label warning or if it was used or prescribed after an FDA recall.
If one of these parties is to blame for your injuries, you have the right to file a product liability claim. If you’re injured through a device and you think any particular medical practitioner is accountable, you have the right to file a medical malpractice lawsuit to hold that the person responsible. If you’ve been injured because of a faulty medical device, you may be qualified for the compensation such as medical expenses, loss income and future profits, punitive damages, pain and suffering, including emotional anguish.
Lawsuit Funding on Defective Medical Devices, Pharmaceuticals and Drugs
If you or a loved one has been injured or killed by a dangerous drug, defective medical device or defective pharmaceutical device, are currently involved in a personal injury lawsuit and are experiencing moderate to severe financial difficulties, we can help. TriMark Legal Funding LLC, The Settlement Funding Company is a leading provider of pre settlement funding and non recourse lawsuit loans throughout the United States. Call today and you could have money in hand in the next 24 to 48 hours.
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.
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