What Sort Of Injuries Can Happen Due To Defective Airbags In Automobiles?

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Airbags installation in the car is needed to offer protection from major injuries. In fact, according to federal safety standards, it is now vital to get airbags installed in all the passenger vehicles.

Airbags cannot stop the mishap but they aid in minimizing major injuries in accidents.

What will you do if airbags are defective? What will happen?

Defective airbags won’t be able to safeguard the occupants of the vehicle and the person might get serious injuries. You can even visit the below-mentioned link if you want to know how Takata airbag lawsuits can help you http://takataairbagrecalllawsuit.com/

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It might cause an airbag to fail when it is needed the most, means during the automobile accident.

During a car accident, airbags inflate faster to provide the driver with a soft cushioning in order to stop their forward motion and reduce any impact-caused injuries.  Earlier the survival rate of passengers involved in a car accident was very low.

Therefore, airbags provide the occupants with a certain level of safety whenever they are inside the vehicle. However, if the airbag fails to deploy when needed, the persons inside the car have nothing to protect and it is life-threatening.

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According to the National Highway Traffic Safety Administration (NHTSA), there have been 11 Takata airbag deaths in the recent years.

You can receive compensation if any of your family members have been subjected to Takata airbag recalls, by filing a Takata airbag lawsuit.

Takata manufactured and supplied these faulty airbags to many companies for years, creating one of the biggest and most complexes recalls in U.S. history. In 2013, a series of death and injuries resulted in Takata airbag recall. If you search on the internet, you will find many experienced experts helping people facing any kind of injury.

 

Lawsuits Filed Against Taxotere Drug Manufacturing Company – Sanofi Aventis

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A widely used chemotherapy drug for cancer made by Sanofi-Aventis called Taxotere is used to treat breast cancer. This drug works by interfering with the expansion and spread of cancer cells in the body. However, many women in the U.S who has taken this drug have suffered hair loss.

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If you want to know more about such cases you may visit this link www.taxoterehairlawsuit.com/ for information. The reason that a lot of women took chemo drug Taxotere because prescribed treatments were only required once every three weeks, as opposed to once a week with other similar drugs.

Why Taxotere Lawsuits were and are still filing against Sanofi Aventis?

The drug Taxotere was first approved by the U.S. FDA in 1996. In December 2015, the FDA accredited reports that associated chemotherapy patients treated with this drug to disfiguring permanent hair loss and also, baldness.

Although every individual who undergoes chemotherapy treatment knows that a common side effect of the treatment is the hair loss, however, they also expect that their hair will start to grow back after six months of completion of the treatment.

The Taxotere hair loss lawsuit claim that the pharmaceutical company which manufactured this drug marketed Taxotere as a superior drug to similar chemo treatments even though they knew about the probable high risk of permanent hair loss, baldness, and alopecia in breast cancer patients.

You may read review here on this link about the Taxotere drug that how it has impacted cancer patients lives that compelled them to file the lawsuit.

You may be eligible for compensation through a lawsuit if you:

  • Were diagnosed with breast cancer
  • Were prescribed Taxotere before December 2015
  • Stopped taking Taxotere at least six months ago
  • Suffer from permanent baldness or partial baldness

The manufacturer also faces allegations to have ultimately misled the public and medical community; which increased the physical and emotional losses breast cancer survivors may experience after treatment.

 

Rising Number Of Knee Replacement Revision Surgeries

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It is a world renowned fact that when medications, therapies and other treatments fail, surgery is the next step to regaining mobility. A total knee replacement can get a persistent back to work or back to his or her better quality of life.

Few years back, a device named depuy knee attune was launched in the market, which was claimed to be the best drive till date and it will help in regaining the knee mobility among all the age groups suffering from walking issues.

Visit https://www.depuykneelawsuit.com/ to find out what actually happened that people after undergoing surgery, suddenly came forward to file lawsuits.

You will find that that was not enough, persons who have suffered from DePuy knee problems like pain, infection, bone loss, amputation, had to undergo revision surgery may be barred to compensation through filing DePuy knee lawsuits.

Anyone person who manages to meet this description is eligible for a free, no-obligation case review with a lawyer managing DePuy knee lawsuits that are national. Knee replacement lawsuits against the subsidiary of Johnson & Johnson are the best means for individual consumers to hold the giant accountable.

Lawyers handling DePuy knee failure suits work on contingency, meaning you never pay fees unless we win compensation for you. DePuy knee lawyers are helping families recuperate the compensation they merit and bring about lasting change.

Defective DePuy Knees

Patients who have been entrenched with defective DePuy knee replacement systems bang a trend of early failure rates. DePuy knee failure signs might have to undergo in the months to years following a knee replacement procedure.

As the manufacturers claim, knee replacement components should last approximately for 15 years or so, but lots of patients reported about pain, swelling, and signs of infection in the two years following their knee replacement.

Revision surgery is obligatory to eliminate defective DePuy knee components, which might result in bone loss and other permanent injuries.

Do not forget to read the full post, as you will get through the deep information on the events that hit Johnson and Johnson, a big global giant for making such life threatening device.

Should You File a Taxotere Hair Loss Lawsuit?

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Taxotere was approved by the FDA in May 1996. The medicine was suggested for the treating patients with advanced or metastatic breasts malignancy after chemotherapy when any another medicine failed. But it has been found to cause permanent alopecia or hair loss in women.

The suits claim, however, that Sanofi allegedly advertised the medication for use in patients with early-stage breasts cancer. The suits also declare that the company advertised the medicine in a far better way than the rivals’ drugs even though studies proved that Taxotere didn’t offer any increased benefits.

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Actually, research posted in the brand new Great Britain Journal of Treatments in 2008 discovered that the competitor medicine of Taxotere, Taxol was actually far better than Taxotere. In 2009, the FDA send Sanofi a caution letter accusing the company of making false and misleading assertions about the effectiveness of its medication.

Across the country, women who consumed Taxotere during chemotherapy are filing lawsuits saying that they have lost their hair permanently due to medication. They’re seeking payment from the maker for mental suffering, bills and for their psychological destruction. If you too are have been cheated by Sanofi, you may file a Taxotere lawsuit by hiring a lawyer via http://www.taxoterehairlawsuit.com/taxotere-lawsuit-lawyers.aspx.

       

The lawsuits are filed to help patients recover money from the drug’s company for the damage they suffered due to their hair loss. The suits claim that the maker of the drug, Sanofi:

  • Paid doctors for prescribing Taxotere for off-label uses to the cancer patients at early stages.
  • Didn’t properly alert patients about the chance of long lasting, chemotherapy-induced alopecia (hair thinning).

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  • Subjected patients to a medication that was more harmful than other alternatives.
  • Trained their team to misrepresent the efficiency of the medicine.
  • Knew that the chance of everlasting hair thinning was much increased with Taxotere than competitor drugs.

As a result, Sanofi is in charge of providing reimbursement to women who experienced long-term hair loss due to the drug usage.

Lawsuits can help women retrieve compensation for injuries that they experienced after losing their hairs. These damages range from:

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  • Mental hurting (anxiety, despair, etc.)
  • Medical expenses, including remedy and counseling
  • Lost of income to work due to emotional destruction
  • Disfigurement
  • Loss of standard of living

The lawsuits can also help ensure that Sanofi and other medication producers market their products for FDA-approved uses only.

Risperdal Causes Male Breast Growth – Cosmetic Surgery Claim

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Risperdal (generically known as risperidone) is an antipsychotic drug that is used to treat delusional psychoses. Dopamine is a key neurotransmitter that the brain uses which allows a person to experience pleasure and desire. Risperdal acts to reduce the amount of dopamine the brain produces so that a natural balance of chemicals in the brain. This can reduce or eliminate many psychotic disorder that people experience.

How Risperdal affect?

The right cause of male breast enlargement among Risperdal users is unidentified, but is claimed that risperidone may boost production level of prolactin; a hormone that produced by the forward pituitary; in females, it induces growth of the mammary glands. As a result, teen boys got increased production of this hormone may also cause breast muscles development and in a few cases cause breast & nipple pain or nipple lactation.

Unfortunately, the use of Risperdal is known to cause several harmful side effects for its users. Dangerous side effects of Risperdal are similar to those of many other antipsychotic medications. Potential fatal side effects include tardive, dyskinesia, extrapyramidal disorders, and serious neuroleptic malignant disorders.

Non-fatal, short-term side effects of Risperdal nausea, anxiety, dizziness, insomnia, low blood pressure, muscle stiffness, fatigue and weight gain. For more information about Risperdal lawsuit, you can also visit http://www.risperdalgynecomastialawsuitcenter.com/risperdal-male-breasts-lawsuit.asp.

A study data released in 2006 in the Journal of Clinical Psychopharmacology provides facts to pay Risperdal court situations that the medicine considerably enhances prolactin creation level, directing to the person boob enhancement.

Medical specialists in the study notified of potential injury: “Risperidone directed at teen at dosages generally used for the healing of psychotic indications can significantly increase prolactin secretion levels, with medical implications for illustration gynecomastia.

So long as the very long time effects of antipsychotic drug-created hyperprolactinemia aren’t well equipped with documents, specifically involving lower bone relative density, infertility, development, and past due puberty, Risperidone should be studied carefully to children and young adults.”

Risperdal Lawsuit Compensation

The first Risperdal gynecomastia lawsuit was filed by a young adult who developed breasts while taking Risperdal between the ages of 9 and 14. The young man required surgery to remove the breast tissue, and suffered from a great degree of social and emotional trauma. This and subsequent Risperdal lawsuits have asserted that Jansen and its parent company Johnson & Johnson failed to adequately warn consumers that boys could grow breasts while taking Risperdal. If you or a loved one developed male breasts while taking Risperdal, you may be entitled to compensation through a Risperdal gynecomastia lawsuit.