Progress of Federal Taxotere Hair Loss Lawsuits

Taxotere Hair Loss

Taxotere Hair Loss Does Additional Harm to Breast Cancer Survivors

It’s there – like a sub audible hum – underneath Sanofi-Aventis’s decision not to disclose the risk of permanent Taxotere hair loss. It will certainly be there, underpinning the drug manufacturer’s offers to settle the lawsuits according to National Trial Lawyers.

The effort to minimize the harm that Taxotere alopecia does to breast cancer survivors, though rarely said aloud, goes a lot like this:

“C’mon. It’s just hair. Aren’t you glad to be alive?”

Permanent baldness can be devastating for women. Hair loss reportedly causes more psychological pain for some breast cancer survivors than the loss of a breast. Yet, evidence suggests that Sanofi-Aventis chose to hide the danger, minimize it, and play it down when it happened.

Motivation is anyone’s guess. It’s just hair, and you know how women can be about that.

Studies show that for women more than men, sexuality, attractiveness, and personality are symbolically linked to hair.

Hair loss can seriously affect self-esteem and body image. In a study of cancer patients with and without alopecia, those with alopecia had a poorer body image and worsening self-concept after the loss.

In other, research about 40 percent of women with alopecia report marital problems as a consequence, and about 63 percent claim to have had career related problems.

Taxotere Hair Loss Lawsuit

Christine tells a more personal story: “I will never forget leaving the dermatologist’s rooms after being told that my lack of hair growth was due to my particular cocktail of chemo drugs, the likely culprit being Taxotere.

I was utterly devastated as I felt I had lost my femininity and aged another 20 years, all at once. It was so much worse than losing a breast to cancer, because that could be fixed – I had undergone a reconstruction.”

The FDA approved Taxotere in 1996. At the time, patient warnings included only information about temporary hair loss. As early as 2009, European labeling for Taxotere warned of cases of permanent alopecia.

Studies over a number of years reported permanent alopecia in between 6 and 15 percent of patients. Not until 2015, however, did the FDA update US safety warnings to include the possibility of permanent baldness.

Were Taxotere the only effective drug on the market to treat breast cancer, patients’ decision-making might have been different. However, studies suggest that paclitaxel (marketed as Taxol in the US) is just as effective at combatting cancer. It appears to be less toxic than Taxotere.

It’s also a generic and cheaper. The choice for patients has not been about life or death, but between treatments that have more and fewer side effects and may cost less.

But Sanofi-Aventis apparently failed in its obligation to warn patients of the risk of permanent alopecia, perhaps because of a misunderstanding about the importance of hair or perhaps because of unexamined assumptions about the importance of patient’s psychological health.

Source Taxotore Hair Loss

Progress of Federal Taxotere Hair Loss Lawsuits

Taxotere Hair Loss Lawsuits Move Forward

Taxotere Hair Loss Lawsuits Move Forward

Plaintiffs involved in litigation revolving around permanent hair loss from the cancer drug Taxotere recently learned the first case in their multi-district litigation has been set for trial in September 2018.

The plaintiffs involved in the litigation have claimed that they were not warned prior to taking Taxotere that it could cause alopecia, a medical condition in which the immune system attacks hair follicles, resulting in hair loss.

While hair loss is often a common occurrence with chemotherapy, plaintiffs have alleged that Taxotere is far more likely to cause permanent alopecia compared to other equally effective cancer drugs.

Taxotere was introduced by Sanofi-Aventis in 1996.

It was approved in the U.S. for the treatment of various cancers: breast cancer, advanced stomach cancer, head and neck cancer, non-small cell lung cancer and metastatic prostate cancer.

Following the expiration of Sanofi’s patent in 2010, the FDA approved marketing of the generic version of Taxotere – docetaxel – the following year.

It wasn’t until 2015 that permanent alopecia was first included as a possible Taxotere side effect was on the drug’s U.S. labeling. Plaintiffs in the MDL have cited several studies, which allegedly demonstrate that Sanofi was aware of the potential for permanent alopecia for years before the label was modified.

It has also been noted by plaintiffs that the European medical community was informed of this risk in 2005, and the Canadian Taxotere label had undergone a similar modification in 2012.

Taxotere Hair Loss Lawsuits

Taxotere Hair Loss

According to studies, the risk of permanent alopecia resulting from taking Taxotere is between 6 and 10 percent. Many of the plaintiffs have claimed that they could have taken other equally effective chemotherapy drugs that wouldn’t have resulted in permanent hair loss, but were never warned of the risks by their oncologists.

The trauma of permanent hair loss for cancer patients is severe, a constant reminder that they remain victims of the disease.

At Saunders & Walker, we continue represent patients harmed by dangerous drugs and defective medical devices.

If you or a loved has taken Taxotere for cancer treatment, and it resulted in permanent hair loss, please contact us immediately for a free consultation.


Taxotere Hair Loss Lawsuit

Taxotere Hair Loss Litigation Continues to Grow

Taxotere Hair Loss Litigation Continues to Grow, with 1,270+ Lawsuits Pending in Federal Multidistrict Litigation

At least 156 new Taxotere lawsuits have been filed in federal court on behalf of cancer survivors who allegedly experienced permanent hair loss following treatment with the widely-used chemotherapy agent.

According to an update issued today by the U.S. Judicial Panel on Multidistrict Litigation (JPML), there are currently 1,272 cases pending in the U.S. District Court, Eastern District of Louisiana, where all federally-filed Taxotere hair loss claims have been centralized for the purpose of coordinated proceedings.

The JPML’s previous updated indicated that 1,116 cases had been filed in the litigation as of June 15th.

Taxotere and Hair Loss

Taxotere is manufactured by Sanofi-Aventis and was approved to treat breast cancer by the U.S. Food & Drug Administration (FDA) in 1996.

The chemotherapy drug has since been approved to treat other cancers, including head and neck cancer, gastric cancer, prostate cancer and non-small cell lung cancer.

Hair Loss Taxotere

While hair loss commonly occurs during chemotherapy, pla­intiffs pursuing these claims charge that alopecia associated with Taxotere is far more likely to be permanent compared with other, equally effective medications.

Mention of permanent alopecia as a possible Taxotere side effect was not included on the drug’s U.S. labeling until December 2015.

Plaintiffs cite several studies which allegedly demonstrate that Sanofi was aware of the potential for persistent alopecia years before the label was modified.

They also point out that that the European medical community was informed of this risk in 2005, while the Canadian Taxotere label underwent a similar modification in 2012.

Taxotere Bellwether Trials

The federal Taxotere litigation was established in October 2016. Initially, just 33 hair loss claims were transferred to the Eastern District of Louisiana.

According to a report from the Louisiana Record, the federal litigation could convene the first Taxotere bellwether trial in September 2018.

These “test” trials are common in large, co litigation, and often involve lawsuits representative of other cases pending in the proceeding. They are intended to gauge the strength of plaintiffs’ claims, and often provide insight into how juries might rule in other lawsuits involving similar questions of facts.