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.
The FDA has discovered links between fluoroquinolone antibiotics and a number of adverse, disabling and potentially irreversible health risks, including:
The side effects can include tendon damage or rupture, permanent nerve damage in the extremities, liver toxicity, kidney failure, hearing or vision problems, or psychiatric side effects.
Many of these symptoms can be irreversible.
Because of the dangerous health risks involved with fluoroquinolones, the FDA recommends that for some more common bacterial infections fluoroquinolones only be used if no other options are viable.
Fluoroquinolones are a very strong form of antibiotics commonly used to stop the growth of bacterial infections.
Fluoroquinolones are the most commonly used form of antibiotics, taken by nearly 33 million consumers in the U.S. annually.
The product contains fluoride, a neurotoxin, which can enter the brain and central nervous system through sensitive tissues.
Fluoroquinolones were first approved to treat a small number of bacterial infections, primarily urinary tract infections.
The antibiotics are now used to treat a wide range of bacterial infections.
Fluoroquinolones are often used when a patient has built up an immunity to other antibiotics, prompting the use of this very strong class of drugs.
Most often, fluoroquinolone antibiotics are used to treat the most severe bacterial infections.
Fluoroquinolones have been linked to serious adverse health effects, including tendon problems and permanent nerve damage.
As a result, the FDA has mandated that all fluoroquinolone drugs carry a black-box label warning consumers of the risks associated with the antibiotics.
Common fluoroquinolones include:
Levaquin was first approved for marketing in 1996.
It accounts for around 28% of all fluoroquinolone prescriptions in the United States, making it the second most popular fluoroquinolone antibiotic.
It was previously the most prescribed antibiotic in 2010, used to treat a range of bacterial infections including:
According to the FDA, a new warning is needed for Levaquin, Cipro, Avelox and other fluoroquinolones (FQs).
This warning is needed because they may trigger a serious, persistent, multi-symptom disability referred to as fluoroquinolones-associated disability (FQAD).
FQAD refers to a “constellation of symptoms” leading to disability that has been observed during FDA monitoring of FQ safety reports.
Although most of the individual symptoms observed are documented in the literature and reflected in the FQ drug medication guides, there have been no warnings in the past about a link to a constellation of symptoms across organ systems.
Case Studies seem to indicate that individuals experience FQAD symptoms differently.
However, a diagnosis of this disability requires an individual to meet the three (3) following criteria:
Case studies note that while some symptoms may appear during the FQ course of treatment, it is not unusual for some individuals to experience symptoms, linked to FQAD, months after treatment has stopped.
In addition, some symptoms progressively worsen over time.
The FDA has received more than 50,000 reports of adverse events and 2,600 reports of deaths associated with Levaquin, Cipro, Avelox, and Factive, through June 30, 2015.
According to FDA estimates only about ten percent of all adverse events are actually reported to the FDA, as these are voluntary reports.
Furthermore, in the case of FQAD, most consumers and many doctors were not aware that there could be a link between a delayed symptom and an FQAD course of treatment.
Therefore, it is possible that the number of adverse events that were actually related to FQ treatments is more than ten times as large as currently reported.
For years, activists and researchers have been trying to get the word out to the public about the risks that these popular billion-dollar drugs carry with them.
Many critics have been public about their belief that FQs, including Levaquin, Cipro, Avelox and Factive (as well as the six other FQs that were removed from the market) are over-prescribed and they should be reserved for conditions in which other effective antibiotics are not available.
The FDA has discovered links between fluoroquinolone antibiotics and a number of adverse, disabling and potentially irreversible health risks.
These irreversible health risks include:
In addition, these can also cause a range of side effects, including:
Many of these symptoms can be irreversible.
Because of the dangerous health risks involved with fluoroquinolones, the FDA recommends that for some more common bacterial infections fluoroquinolones only be used if no other options are viable.
TorHoerman Law is no longer accepting clients for fluoroquinolone lawsuits, including Levaquin products.
Previously filed lawsuits were filed on behalf of patients who are/were prescribed Levaquin products and suffered the following injuries:
The fluoroquinolone lawsuits against the manufacturer of Levaquin claimed that patients suffered aortic dissection / aortic aneurysm that resulted in hospitalization, surgery, or death within one year after taking the antibiotics.
The fluoroquinolone lawsuit further claims that the manufacturer failed to warn patients of the potential for these injuries.
Studies suggest that individuals who are prescribed fluoroquinolone are two times as likely to develop these dangerous aortic conditions.
The fluoroquinolone lawsuit claims that manufacturer of Levaquin:
TorHoerman Law is no longer accepting new clients for the Fluoroquinolone Lawsuit.
Owner & Attorney - TorHoerman Law
Here, at TorHoerman Law, we’re committed to helping victims get the justice they deserve.
Since 2009, we have successfully collected over $4 Billion in verdicts and settlements on behalf of injured individuals.
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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.
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In this case, we were able to successfully recover $20 Million for our client after they suffered a Toxic Tort Injury due to chemical exposure.
In this case, we were able to successfully recover $103.8 Million for our client after they suffered a COX-2 Inhibitors Injury.
In this case, we were able to successfully recover $4 Million for our client after they suffered a Traumatic Brain Injury while at daycare.
In this case, we were able to successfully recover $2.8 Million for our client after they suffered an injury due to a Defective Heart Device.
Here, at TorHoerman Law, we’re committed to helping victims get the justice they deserve.
Since 2009, we have successfully collected over $4 Billion in verdicts and settlements on behalf of injured individuals.
Would you like our help?
We're ready to fight for you. We're ready to be your ally. And we're ready to start right now.
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