An IVC filter, also known as an inferior vena cava filter, is a medical device that is surgically implanted into a patient who is at risk of blood clots, especially those that can go to the heart and lungs. It is obvious that this device’s task is to keep a patient safe, but it is just sad that it can also be a device that can cause a patient harm.
It has been proven that there are defective IVC filters, such as the Bard G2 IVC filters, resulting into unwarranted bodily complications and Bard G2 IVC filter lawsuits. But what exactly are these defects, and what do they cause to the body?
- Device migration – The device is quite thin, so it is not surprising that it can accidentally migrate to another part of the body. If it is in another part of the body, it cannot function properly and may require long hours of retrieval, especially if the body part it has migrated to is not easily accessible.
- Filter breakage – The fragility and spider-like design of the product also puts the device vulnerable to breakage and fractures. Entire breakages can be more dangerous, because the spider-like legs can also migrate to other parts of the body, and worse, inflict damage to the migrated body part.
- Perforation – The spider-like legs of the device can pierce unsuspecting blood vessels, tissues, and even entire organs. The patient even becomes more vulnerable to perforation during device migration and filter breakage.
According to the website of the medical product lawyers of Habush Habush & Rottier, the Bard G2 IVC filter problems can result into complications, such as internal bleeding. They can also help in the formation of more blood clots, so instead of helping the patient from blood clots, the IVC filter is making the patient even more vulnerable to it.
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Millions of patients rely on the pharmaceutical industry to create solutions to their important medical needs. Typically, these solutions help individuals successfully receive treatment and live fuller lives. There are, however, certain moments when pharmaceutical solutions also lead to unforeseen side effects and cause even more hardship and devastation. In fact, these defective pharmaceutical solutions often constitute to a majority of the product liability lawsuits filed in courts all over America.
Despite advancements in the field, there are still some drugs and medications that can cause serious issues for a significant number of patients in the United States. Most of the time, problems with defective pharmaceuticals are missed because of missteps in research and testing. Even when a pharmaceutical product has been approved by the Food and Drug Administration (FDA), there is no certainty that it will be completely safe from side effects.
In most cases, the devastating effects of defective pharmaceuticals are due to mistakes committed by manufacturers. There are several pharmaceutical companies that market certain products for off-label use—treatments that are yet to be explicitly approved by the FDA because of lack of adequate testing. According to the website of Williams Kherkher, one such example is the Stryker hip implant. Another pharmaceutical product often the subject of product liability suits is the anti-psychotic drug called Risperdal. As pointed out by the website of the lawyers of Williams Kherkher, the continued off-label use of the drug has led to several cases of serious medical conditions like gynecomastia and hyperglycemia.
It is a horrifying thought to consider that the products intended to treat patients can cause other medical conditions that could be far more serious than what they originally had. As such, it’s important for affected individuals to seek out legal counsel as soon as possible. The dangers of defective pharmaceuticals should never be ignored. Manufactures should be continuously held accountable for falling short of the high standards require of their profession.
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