You may be eligible to file a Tylenol Autism ADHD Lawsuit / Acetaminophen Autism ADHD Claim if you or a loved one used Tylenol and/ or Acetaminophen during pregnancy, and your child was subsequently diagnosed with ADHD or Autism Spectrum Disorder.
Legal action is being strategized by our attorneys for Horizon Therapeutics’ failure to properly warn patients of potential hearing loss side effects.
You may be eligible to file a Tepezza Lawsuit if you or a loved one took Tepezza and subsequently suffered permanent hearing loss or tinnitus.
If you or a loved one took Elmiron and subsequently suffered vision loss, blindness, or any other eye injury linked to the prescription drug.
Contact the Elmiron Lawyers from TorHoerman Law.
Get a free online case evaluation and find out if you qualify for compensation instanly.
You may qualify to participate in a 3M Combat Arms Earplugs Lawsuit if:
Over 140,000 Exactech hip, knee and ankle implants have been recalled due to packaging errors that can lead to the breakdown of parts vital to the device’s function.
If you or a loved one suffered injuries from an Exactech implant device, you may be entitled to financial compensation.
You may be eligible to file a Hair Straightener Cancer Lawsuit if you or a loved one used chemical hair straighteners, hair relaxers, or other similar hair products, and subsequently were diagnosed with:
Get a free online case evaluation and find out if you qualify for compensation instanly.
Over one million people, who were present at Camp Lejeune (North Carolina) between 1953 and 1987, may have been exposed to toxic substances in the water.
The Camp Lejeune Contaminated Water Lawsuit can apply to you, a family member, or a loved one who lived at Camp Lejeune (North Carolina) and suffered health effects from the decades of water contamination that occurred.
Toxic chemicals in Aqueous Film-Forming Foam (AFFF Firefighting Foam) have been linked to numerous types of cancer, including:
AFFF Firefighting Foam lawsuits aim to hold manufacturers accountable for putting peoples’ health at risk.
If you have been exposed to Paraquat and diagnosed with Parkinson’s disease may be eligible to pursue compensation, and entitled to participate in the paraquat lawsuit.
Contact us today to see if you qualify for the Paraquat Parkinson’s Disease Lawsuit!
Get a free online case evaluation and find out if you qualify for compensation instanly.
Our firm is about people. That is our motto and that will always be our reality.
We do our best to get to know our clients, understand their situations, and get them the compensation they deserve.
At TorHoerman Law, we believe that if we continue to focus on the people that we represent, and continue to be true to the people that we are – justice will always be served.
Without our team, we would’nt be able to provide our clients with anything close to the level of service they receive when they work with us.
The THL Team commits to the sincere belief that those injured by the misconduct of others, especially large corporate profit mongers, deserve justice for their injuries.
Our team is what has made TorHoerman Law a very special place since 2009.
Get a free online case evaluation and find out if you qualify for compensation instanly.
If you have suffered any of the aforementioned injuries as a result of your Essure device, you may be able to participate in the Essure lawsuit.
To find out whether you qualify, contact the offices of TorHoerman Law.
Our firm offers free no-obligation Essure lawsuit consultations.
We can help determine whether you have a case against Bayer and help get you on the right path to take legal action if necessary.
Essure birth control is a permanent sterilization device made of two tiny metal coils that are inserted into a woman’s fallopian tubes.
The coils contain a material that stimulates inflammation and scarring, causing the tubes to close up and stop sperm from reaching the woman’s eggs.
In theory, Essure birth control should prevent pregnancy, but there have been close to 750 reports of “E-babies” since the device was approved in 2002.
Essure was first manufactured and sold by Conceptus, Inc. under the name Selective Tubal Occlusion Procedure or “S/TOP” Permanent Contraception device.
In April 2013, Bayer AG agreed to buy Conceptus Inc. for $1.1 billion so they could add the Essure device to their women’s health division, which also includes Mirena IUD (also the subject of lawsuits filed by injured women).
As of 2013, there have been more than 750,000 Essure procedures performed worldwide since FDA Approval in 2002.
The FDA is charged with the monitoring of the safety and efficacy of medical devices such as the Essure implant.
Essure was first manufactured and sold by Conceptus, Inc. under the name Selective Tubal Occlusion Procedure or “S/TOP” Permanent Contraception device.
In April 2013, Bayer AG agreed to buy Conceptus Inc. for $1.1 billion so they could acquire the permanent contraception device to their products, which also includes the Mirena IUD, which has also been the subject of a number of Mirena IUD lawsuits by injured women.
Conceptus Inc. was granted “Premarket Approval” (PMA) of the Essure device.
In addition to the information provided to the FDA at the time of approval, Conceptus (and later Bayer) agreed to provide additional information after the marketing of the device.
Failure to meet post-marketing requirements would result in the device being considered “adulterated” as defined by the FDA.
An adulterated device would invalidate the PMA and would need to be removed from the market.
The following injuries are listed in the claims against Essure:
These injuries have been named in the Essure lawsuit.
However, not all have are included on the device label and have not definitively been proven to be associated with Essure.
Essure birth control is a type of sterilization that does not require an incision/cut.
It is referred to as hysteroscopic sterilization.
During the 10 minute Essure procedure, a health care provider inserts a small, rigid, tube-like instrument called a hysteroscope into the vagina and through the cervix.
Small metal coil inserts are placed in the opening of the fallopian tubes.
Essure birth control is a permanent form of birth control and removal of the Essure device is tricky according to several doctors consulting E-sister on the “Essure Problems” Facebook Community Page.
Dr. Shawn Tassone and Dr. Julio Novoa are Obstetrician-Gynecologists who note that they have seen some crazy Essure device removal methods over the years.
Dr. Tassone and Dr. Novoa warn women to see a doctor that has been educated to remove the Essure device and provide helpful insight into removal methods and tests that should be run prior to Essure removal.
Dr. Julio Novoa compares the Essure device to an industrial piece of Velcro attached to a cotton ball.
Even if you separate the cotton ball from the Velcro, you will always have tiny pieces of the cotton ball on the Velcro.
For this reason, Dr. Novoa recommends that the Essure device is removed intact.
The number of women experiencing complications continues to grow and their stories become increasingly visible thanks to social media.
There are now more than 25,000 members of a closed Facebook Group called “Essure Problems”.
E-sisters on Facebook mention similar problems like those reported to the FDA including:
In addition, women report a large number of Essure device problems including:
In one FDA reported case, a woman with no prior medical issues convulsed and suddenly died during the placement of Essure.
Autopsy results showed uterine perforation and blood in the abdomen.
These complications are mentioned in the claims against Essure but have not been proven to be associated risks of Essure at this time.
All known risks were are included in Essure’s warning label.
In April 2015, a 5-year post-market study of Essure was published.
Following the study’s publication, the FDA decided to rebrand Essure as a surgical device and required that the device include more comprehensive instructions for op/post-op.
In October 2015, an independent study found that women who received Essure are 10-times more likely of needing a second operation as compared to women who received tubal ligation.
In February 2016, the FDA required Bayer to conduct further post-market research after receiving a number of concerning adverse event reports.
Bayer’s studies find that less than 1% of case report data related to pain, bleeding, device placement or migration and pregnancy were altered.
Joining the activists in the cause for removal of Essure are lawyers who are taking the fight to the courts.
Lawyers representing women injured by Essure are hopeful that Bayer will be held accountable for its defective and unreasonably dangerous product.
Despite the numbers of injured women, the Essure lawsuit against Conceptus/Bayer is facing an uphill battle.
Conceptus/Bayer has a powerful defense on their side – Federal Preemption that may prevent women from pursuing their cases in state courts.
Despite the uphill battle, lawyers are currently filing cases in a number of state courts arguing that Bayer/Conceptus violated the terms of their FDA approval and therefore forfeited protection under preemption laws.
There are currently more than 10,600 lawsuits filed against Essure (Oct. 2017).
Barring statute of limitations violations, cases are still being filed on behalf of individuals injured by Essure.
Plaintiffs in the Essure lawsuit claim that Bayer is guilty of negligence and also of failing to warn the public about the risks associated with Essure.
Furthermore, the lawsuits claim that the manufacturer falsified documents in order to get market approval for Essure.
Most of what is known today about Essure complications are a result of the grassroots efforts of activists that refer to themselves as “E-Sisters.”
Websites and Facebook community pages have been set up as support networks for women that have been injured by Essure.
In addition, many of these same advocates are behind a nonprofit advocacy group, ASHES (Advocating Safety in Healthcare E-sisters) that is raising money to continue to advocate on behalf of injured E-sisters.
Grassroots advocacy has led to an increase in filed FDA adverse event reports. Advocates encourage every injured E-sister to file voluntary FDA reports so that the FDA is aware of the extent of the problem.
Increasing patient engagement through online communities and reporting has not gone unnoticed by the FDA or Congress.
On September 24, 2015, nearly 13 years after Essure’s approval, the FDA’s Obstetrics and Gynecology Device Advisory Panel met to consider the large increase in adverse event reports related to Essure.
Numerous patients and interested individuals gave emotional testimony at the September advisory panel meeting and additional 2,833-interested individuals posted their Essure stories to a public docket.
The public docket is now closed but the stories of women that were not warned of the dangers of Essure remain available for public viewing.
The FDA will announce its findings from the advisory panel at the end of February 2016.
In addition, E-sisters continue to take their grassroots efforts to Congress getting the support of U.S. Rep Mike Fitzpatrick who presented Congress with a bill ordering the withdrawal of Essure from the market.
Essure advocates continue to contact congressmen at their local levels in hopes of getting support for Essure removal.
Essure advocates have also captured the attention of Erin Brockovich, who dedicates a website to the stories and voices of women facing serious medical issues after being implanted with the Essure device.
These stories are meant to save thousands of women from making a birth control decision that could negatively impact their health.
Although Essure has been removed from every market except in the United States, advocates continue to spread the word about the dangers of Essure to make sure that women facing birth control decisions are given full information about the devastating side effects of the device.
Owner & Attorney - TorHoerman Law
TorHoerman Law was responsible for handling a medical case for our family. I was extremely impressed with their professionalism and ability to react quickly. They also did a nice job keeping us updated with the case throughout the process. This was the first time experiencing a situation like this and Tor Hoerman law did an excellent job from start to finish.
TorHoerman Law is an extraordinary law firm – a firm that truly makes the client’s best interests the primary concern. Their team of personal injury lawyers are experienced, personable, and well versed in a range of litigation areas. They are supported by a dedicated team of staff that are as equally friendly and helpful. I would recommend TorHoerman Law for any personal injury litigation needs.
All of my questions were answered quickly and in a way I could understand. Steve and the entire staff were friendly and professional.
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