Table of Contents
Have you been blindsided by the dark side of a ‘miracle’ drug? Untwist the twisted tale of Humira, the blockbuster medication that promised relief but delivered a world of pain.
Join us as we delve into the heart of the Humira lawsuits, where thousands of patients are standing up and fighting against the pharmaceutical company that destroyed their lives. It’s time to break the silence and clear up the hidden dangers lurking beneath the surface of this drug.
What is Humira?
Humira (adalimumab), a prescription medication manufactured by Abbott Pharmaceuticals, was given the U.S. Food and Drug Administration approval to treat rheumatoid arthritis in 2002.
Humira is a member of the class of medications known as tumor necrosis factor (TNF) blockers.
How Humira works? It functions by binding to and obstructing TNF molecules.
Humira is available in three forms, prefilled vials, pens, and syringes. There seems to be one dose of Humira in each pen, syringe, and vial.
How often Humira injections given? A single HUMIRA Pen or syringe (40 mg) administered every other week is the recommended dosage.
Humira has become one of the world’s best-selling drugs, generating billions of dollars in annual revenue. The medicine brought Abbott Laboratories approximately $20 billion in revenue in 2020.
Humira is used to treat several autoimmune disorders such as rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, juvenile idiopathic arthritis, Crohn’s disease, plaque psoriasis, ulcerative colitis, and a skin condition known as hidradenitis suppurativa.
If you have a particular kind of arthritis or a condition that is linked with inflammation, your doctor could suggest Humira for you.
Reported Side Effects and Complications of Humira
View this post on Instagram
Like most prescribed medications, Humira also has minor and major adverse effects. Reactions at the injection sites are one of the most frequent side effects of Humira. Cancer, fungal infections, heart failure, and nerve damage may all be made more likely by Humira.
Humira is known to carry a risk of serious, potentially deadly infections. These harmful infections could be brought on by bacteria, fungus, or viruses. Humira began to warn about the higher risk of fungal infections in its labelling in 2008.
Long-term usage of Humira may greatly enhance the risk of infection because it is specifically made to suppress the immune system. The immune system may be suppressed by TNF-alpha suppression, thereby raising the risk of serious or fatal infections like bacterial, fungal, or TB.
Some patients who took TNF blockers like Humira reportedly experienced Legionella pneumonia. The FDA found 80 patients with Legionella pneumonia who had been medicated with TNF blockers between 1999 and 2010 after completing a review of their Adverse Event Reporting System (AERS) database.
After taking Humira, some patients have developed cancers such as lymphoma and skin cancer. Research has produced contradictory findings about the relationship between Humira and cancer; therefore, the topic is still up for debate.
The FDA released a safety communication as a result of some reports of young people getting hepatosplenic T-cell lymphoma, a rare kind of white blood cell cancer. This type of cancer is extremely deadly and aggressive. T-cell lymphoma can also affect the liver, spleen, and bone marrow, which can cause the patient’s bones to become fragile and potentially breakable. T-cell lymphoma almost generally leads to fatalities.
According to a study, the chance of developing cancer or tumors increases with increasing Humira dosage.
Humira may result in the onset of new heart failure or aggravate existing heart failure in patients.
Humira has not been formally examined in individuals with congestive heart failure (CHF); however, the drug’s label does contain a warning about incidents of worsening CHF.
If you have heart failure, your doctor will need to keep a careful eye on you while you take Humira.
Customers are warned by Humira’s label that demyelinating diseases of the central and peripheral nervous systems have been linked to the medication. Humira may lead to “peripheral neuropathy,” a type of irreversible nerve damage. Individuals who have this injury frequently experience numbness, tingling, or persistent, and crippling pain.
Many people have mentioned neurological adverse effects, including optic neuritis, multiple sclerosis, and Guillain-Barre syndrome. With the treatment of Humira, some patients reported having these conditions’ symptoms for the first time, whereas others saw an escalation of their pre-existing symptoms.
Humira Black Box Warning
Humira tried to be transparent by disclosing any possible health hazards, but it ultimately fell short. They listed “certain” dangers, also referred to as black box terms, on their labeling.
the main 2 side effects of humira ????????????? fml pic.twitter.com/Esq3kUvLWq
— gözde (@iblewurdad) July 4, 2022
The U.S. Food and Drug Administration is aware that Humira is a hazardous drug that could have fatal side effects. As a result, the FDA issued a black box warning requiring the addition of informational packaging inserts with the medications.
The Black Box Warning is printed on the Humira medication states that there is a higher chance of contracting deadly infections like tuberculosis (TB), bacterial sepsis, invasive fungal infections (like histoplasmosis), and infections brought on by other opportunistic pathogens, which can result in hospitalization or death.
It was a little late when Abbott Laboratories officially disclosed the dangers. Many individuals had diseases that weren’t included on the labels of their drugs.
Considering the use of Humira, Abbott has been the subject of several humira heart failure lawsuits. A thorough examination of the medical records is a key component of Humira lawsuits preparation. Medical records are a crucial source of proof regarding your health history, treatments, and effects of Humira.
Allegations against the Manufacturer of Humira
Is there a lawsuit against humira? The two main issues raised by Humira lawsuits are the drug’s adverse effects and insufficient warnings. These lawsuits against Humira contend that AbbVie misrepresented the risks connected to the drug and that patients, as a result, developed major consequences.
Several plaintiffs allege that using Humira caused them to experience adverse reactions, which they claim AbbVie failed to adequately disclose. The trouble with Humira’s concealment is that Abbott kept up its marketing effort while being aware of its potential health hazards.
Patients who took Humira medicine and later had multiple of these side effects started suing Abbott over the past few years. According to evidence that has been revealed, the FDA started sending Abbott complaints about adverse effects they received from patients as early as 2002, yet the medication was neither taken off the market nor changed in any way.
AbbVie concealed the risk that the medication could result in severe side effects, including brain damage and visual issues. Hepatitis B, lymphoma, fungus infections, and potentially cancer are some other unknown risks.
Humira Lawsuits: Settlements and Verdicts
A personal injury case resulted in a $2.24 million settlement for the family of a woman who passed away as a result of Humira side effects.
Delores Tietz, the victim, reportedly received Humira to treat her rheumatoid arthritis, according to the lawsuit. Milton Tietz, who had brought the personal injury claim on his wife’s behalf, won the jury’s verdict in favor of him against Humira.
According to Californian regulators, AbbVie has agreed to pay $24 million to settle accusations that it committed fraud by not revealing all of Humira’s side effects when advertising the popular anti-inflammatory medicine.
What to Do If You are Injured by Humira?
It’s crucial to take care of your health. Contact a qualified doctor to determine your condition, obtain the proper care, and record any possible Humira complications.
Keep up with all of your symptoms, doctor visits, and therapies. This includes the dates and length of time you used Humira, any adverse effects you encountered, and any diagnoses or treatments you obtained as a result of Humira-related issues.
If Humira has affected you, speak with a qualified Humira lawsuit attorney who focuses on personal injury. They can assist you through the complexities of the legal system, advise you on your legal rights, and decide whether you have a strong case.
It may be possible for a person to receive compensation for any injuries sustained as a result of taking Humira if they have been harmed as a result. Compensatory damages are the most typical sort of damages that a plaintiff in a class action may be awarded.
Save all information associated with your Humira prescription, including prescription packaging, pharmacy receipts, and medical records. Building a strong case will require this evidence in a big way.
A complete medical record review is essential for constructing strong Humira lawsuits because it provides the necessary proof of the medication’s effects on your health. The probability of a successful conclusion can be increased by working with experienced Humira lawsuit lawyers to ensure that this process is carried out precisely and completely.
To wrap things up,
The unfolding Humira lawsuits have twinkled a spotlight on the complex intersection of medical advancements, corporate responsibility, and patients’ rights. As the legal battles continue, it’s crucial to stay informed and vigilant to ensure justice is served and the interests of those affected by the drug are protected.
After all, at the heart of every Humira lymphoma lawsuit lies the collective cry for fairness and accountability. In this ever-evolving story, knowledge truly is power. So, let’s keep the conversation going and champion the cause for a healthier, more transparent future for all.
Remember, in the world of Humira lawsuits, staying silent is not an option.
Join our growing Instagram community!
View this post on Instagram