When Pradaxa was first released on the market in 2010, it was marketed as the perfect blood thinning agent. Unlike Warfarin, the most commonly used blood thinner on the market, Pradaxa would not require continual blood test monitoring for liver and kidney problems. Pradaxa was specifically marketed as a blood thinning medication for people that suffer from arterial fibrillation.
Problems Quickly Arise After Pradaxa is Released
Shortly after Pradaxa was released, the Food and Drug Administration (FDA) began receiving adverse event reports. Patients taking the medication were suffering from internal bleeding and dying from strokes, the very thing that Pradaxa was meant to prevent. It was soon discovered that Pradaxa did not have an antidote, so patients who reacted to the medication could not stop its effects.
Additionally, it was soon discovered that it was unsafe for patients to stop taking the medication. Patients who could not stop were forced to delay or refuse emergency medical surgeries or dental surgeries because they could not stop the bleeding.
By 2012, over 500 deaths were directly linked to the medication and the FDA stated that between most drugs, the Pradaxa adverse effects had the largest in volume, found in the reports coming into the agency.
Pradaxa has been associated with increased incidence of death, stroke, intracranial bleeding, and internal bleeding that cannot be stopped. The FDA has since issued a Black Box warning on Pradaxa as it conducts further testing to see if it should be removed from the marketplace.
Dangerous Medications And Patient Rights
When a pharmaceutical company releases a medication that has such a large negative impact on users, it is considered an act of negligence. Patients who have been injured by this medication have the right to seek compensation from these pharmaceutical companies. Families that have lost a loved one due to a dangerous medication have the right to see damages for wrongful death.
A personal injury attorney that specializes in dangerous medications can review the facts of your case and tell you what rights you have against this negligent act by the manufacturer of the drug. Since personal injury laws differ from state to state, you will have different rights based upon your state laws.
Due to the large amount of complaints against the makers of Pradaxa, it is possible that you may wish to join a class action lawsuit against the makers instead of suing on your own behalf. In many ways, a class action suit allows you to seek larger damages and gain other rights you may not have had as a single Plaintiff. During your consultation your attorney will explain all of your options and make a recommendation that will be most beneficial to your case.
If you are currently taking Pradaxa, you are encouraged to speak with your physician about the risks associated with this drug and determine if there are other options that may be more beneficial to you and your overall health. Do not stop taking Pradaxa without talking to your physician. Quitting Pradaxa without an alternative blood thinning agent can lead to immediate blood clotting and stroke or possible death.
Jennifer Alston has researched several manufactured drugs on the market, and has found serious side effects should be explained, in detail to consumers. If anyone you know is being treated with this drug and you would like to know more about complications, search Pradaxa adverse effects on the internet.