A California man who says that Roundup weed killer gave him cancer was just awarded $80 million in damages in his lawsuit.
In the lawsuit, which was filed in federal court in San Francisco, 70 year-old Edwin Hardeman claimed that Roundup caused his non-Hodgkin’s lymphoma cancer. Mr. Hardeman said that he frequently used Roundup weed killer products to treat weeds, overgrowth and poison ivy in his property for years.
Roundup is the most popular weed killer worldwide, and it is manufactured by U.S.-based Monsanto Corporation, which was recently acquired by German-based Bayer Corporation. The agribusiness giants market the weed killer around the globe to consumers.
The active ingredient at issue in the Roundup weed killer is glyphosate. Plaintiffs in lawsuits around the country are alleging that this chemical compound is a carcinogen.
After hearing testimony, the jury concluded that the Roundup product was a “substantial factor” in causing Mr. Hardeman’s cancer.
In a statement following the verdict, Monsanto said that it stands by its product. The agribusiness giant affirmed that the weed killer is safe for personal use, and that it will appeal the jury’s decision. Monsanto highlighted that regulators from around the world, including recently in the United States, have concluded that glyphosate and glyphosate-based herbicides do not cause cancer.
Monsanto is citing decisions by government regulators who have rejected a causal link between Roundup and cancer. They also claim that hundreds of scientific studies support their conclusion that glyphosate does not cause cancer.
But other studies show otherwise. For example, in 2015, the World Health Organization’s International Agency for Research on Cancer determined that glyphosate (the active ingredient in Roundup) is a “probably” carcinogen for humans.
But Monsanto and Bayer have called that conclusion an “outlier” and point to the decisions of other regulators finding no connection between glyphosate and cancer. Recently, the Trump administration’s Environmental Protection Agency found that glyphosate is safe for humans to use, when following the product label warnings and instructions.
Experts say that this case could help drive forward the thousands of other lawsuits that are currently active against Monsanto and Bayer for the Roundup product. There are currently more than 11,200 active lawsuits in the United States against the companies, all of which allege that Roundup caused cancer or sickness. Experts have estimated the settlement cost of all of these lawsuits at more than $5 billion.
So far, only one other case against the makers of Roundup has made it to the trial phase; there, a jury awarded the plaintiff $289 million, concluding that Roundup caused his cancer. (A judge later cut those damages to $78 million, and Monsanto is currently appealing.)
Importantly, the judge presiding over Mr. Hardeman’s case currently has hundreds of other Roundup lawsuits on his docket. He has previously called Mr. Hardeman’s lawsuit as a “bellwether trial,” meaning that it could signal how the other hundreds of cases to come could be determined. This verdict against Monsanto, therefore, could signal a more successful path forward for the other cases still awaiting trial.
Sunbeam Crockpots Recalled for Burn Injuries
Sunbeam Products has issued a recall of one of its crock pot products due to a burn hazard. The recall came just two days before the Thanksgiving holiday, during a time when crock pots are often in use.
Details of the Crock Pot Recall
The product involved in the recall is the Crock-Pot 6-Quart Express Multi-Cooker. Almost one million of these defective products have been sold. According to the recall, the multi-cooker may pressurize if the lid hasn’t been locked in place completely. The pressure can make the lid to detach when the crock pot is in use. If the hot food or liquid ejects from the pot, it can lead to serious burns.
The recall impacts mostly purchases in the US with almost 29,000 in Canada. The cookers were bought at Walmart, Target and online at Amazon as well as other national retailers. The timeline was from July 2017 and up to the time of the recall. The crock put costs between $70 and $100. To find out if your crock pot is part of the recall, you can look at the bottom of the base or on the electrical plug on one of the prongs for the codes K196JN through K365JN and L001JN through L273JN.
It’s advised that anyone with this product not use it as a pressure cooker, but it can be used for sauted and slow cooking recipes. The company will send lids to consumers for free to replace the defective ones if they contact the manufacturer.
The recall notice advised that if consumers use the product as a pressure cooker, they should make sure the lid is in the fully locked position. They can tell if it is secured by making sure the arrow on the lid is aligned with the lock on the base.
Burn Injuries and the Serious Consequences
Sunbeam has gotten more than 100 reports where the lid detached in use. This resulted in almost 100 burn injuries. These burns range from first-degree to third-degree.
A first-degree burn is considered superficial because it only impacts the first layer of skin. This type of injury may not require medical care, but it can be quite painful. However, some cases may require a visit to the doctor or hospital if it covers a large area or hurts too much. Third-degree burns are much more serious and require immediate medical care because the burn impacts the other layers of skin. Infection is often a major concern with third-degree burns as well as other complications.
A person with a third-degree burn may feel a great deal of pain, but it can also be numb. There is often scarring from this type of burn. However, any burn can be considered serious if not taken care of properly.
While many products are recalled and often ignored, this recall from Sunbeam is considered serious and should not be taken lightly. Anyone with one of these products is at risk for serious and permanent injury.
Traumatic Brain Injury May Increase Risk of Alzheimer’s Disease
According to a new study, people who have had a history of traumatic brain injury, otherwise known as TBI, have an increased risk for developing some type of dementia, including Alzheimer’s disease. The research indicates it may accelerate the onset of the disease by about four years.
TBI and Dementia
Dementia is a general term that may include multiple diseases. All have one thing in common – they include a decline in mental ability. This decline is serious enough that it interferes with their ability to act and interact in daily life as it progresses. One of the most well-known conditions under the term dementia is Alzheimer’s disease.
The causes of dementia can vary but all are triggered by abnormal changes in the brain. They result in a loss of cognitive skills or the ability to think. The loss also impacts the person’s feelings, behaviors and even their relationships with others.
A TBI is caused by a sudden impact to the head. It can happen from a fall or car accident as well as other situations where the person hits their head. A person who experiences a TBI may lose consciousness even for only a few seconds. They may suffer from other symptoms:
- Trouble speaking clearly
- Unable to recall the event that caused the TBI
- Difficulty learning or remembering new information
- Lack of coordination
- Difficulty seeing clearly
- Trouble hearing or ringing in the ears
- Unsteady when walking or standing
A TBI can cause issues even years later when the person seems to have recovered from the injury. A doctor will label a TBI as mild, moderate or severe based on various factors, including how long they were unconscious and severity of other symptoms. However, it is important to understand that even a mild TBI can have serious effects that are long-lasting.
Mild to Severe TBIs
A mild TBI is known as a concussion and it doesn’t result in unconsciousness at all or for more than 30 minutes. The person may experience dizziness or a headache, nausea and confusion, but the symptoms go away in a few hours or days. However, in some cases, they can last for several months.
A moderate TBI causes unconsciousness that lasts between 30 minutes and 24 hours with a severe TBI being over 24 hours of unconsciousness. They have the same symptoms as the mild version, only stronger and may last longer.
The ability to learn new information or remember things and to pay attention are symptoms that can be long-lasting or permanent from a TBI. The person may have difficulty organizing their thoughts or being able to create a plan.
Research in the past had linked moderate to severe TBIs with dementia. New research shows that even a mild TBI or repeated mild TBIs may result in an increased risk for developing some type of dementia. Research shows that a protein seen in Alzheimer’s patients is evident within hours of a mild TBI event. Not everyone who has a TBI will develop dementia, but it is important to be aware of the risk.
Bayer Settles 90% of U.S. Essure Claims for 1.6 Billion
About 90 percent of the more than 39,000 lawsuits filed against Bayer over Essure injuries have been resolved by a $1.6 billion settlement. Bayer said in a statement that the settlement resolves most filed and unfiled cases and that it continues to work with plaintiff’s lawyers to resolve the remaining cases.
FDA Actions and Essure Injury Complaints
The settlement comes after years of complains of adverse events involving the metal coils which are placed in the fallopian tubes. Some of these complaints say that the coils can perforate the tubes, tear the uterus, and that the coils can break causing little metal shards to migrate elsewhere in the body. Women have also complained of heavy bleeding, pain, and other side effects that the patients were forced to undergo hysterectomy.
In 2018, the U.S. Food and Drug Administration placed restrictions on the device and required patients to review the Patient- Doctor Discussion Checklist and sign prior to being implanted with the birth control device. Bayer made the decision to stop selling Essure in the United States not long after citing declining sales.
Post-Market Surveillance Reports
The required 522 study, a post-marketing surveillance plan, was also extended by the FDA from three to five years. The FDA published the first spreadsheet of Essure adverse events on August 11, 2020, which includes events that Bayer knew or learns of during the period of November 2016 to November 2020.
The first spreadsheet includes more than 1,400 events including pain, device fragments, pregnancy, and organ perforations, including 1376 reports of serious injury, 53 reports of death and 24 reports of malfunction.
Essure Lawsuit Settlement
Many of the plaintiffs alleged in court filings that Bayer knew or should have known about the risk of adverse events, including organ perforation, device breakage, and device migration. They also allege that Essure birth control was improperly design and can break and migrate after being implanted. They accused Bayer of misrepresenting the efficacy and safety of the contraceptive device and Women who suffered Essure injuries alleged in court filings that Bayer concealed the risks and dangers of the device from the FDA, the medical community and from the women who relied on the device.
Many of the terms of the settlement are confidential, and Bayer did not admit to any wrongdoing in the court filings.
Defective Products4 years ago
Dehumidifier Recall: Several Brand Name Humidifiers are Recalled as a Fire Hazard
Medical Devices5 years ago
Complications from Hernia Mesh
Covid-193 years ago
Metformin as Potential Protector from COVID-19
Covid-193 years ago
Moderna Seeks Emergency Approval for COVID Vaccine
Prescription Drugs3 years ago
Recall for Drug Mix-up with Serious Effects
Prescription Drugs3 years ago
Some Heart Meds May Come with Extra Risk
Nursing Home Abuse4 years ago
Hundreds of Allegations at Georgia Elder Care Facilities Being Investigated
Prescription Drugs3 years ago
Senate Bill May Give More Authority to the FDA for Drug Recall