Depo-Provera Lawsuit
Depo-Provera lawsuits claim brand name Depo-Provera birth control, or its generic forms, may increase the risk of rare brain tumors called meningiomas. Lawyers claim Pfizer didn’t properly warn about the risk. Litigation is in the early phases and there have been no settlements or jury verdicts yet.
See if you qualify for a Depo-Provera lawsuit.
If you or a loved one were diagnosed with meningioma after use of Depo-Provera or Depo-SubQ Provera, you may be eligible for compensation. Fill out the form to get a free case review.
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Latest Depo-Provera Birth Control Lawsuit Updates
As of November 2024, Depo-Provera brain tumor lawsuits are still in the early stages. Lawyers are investigating cases from people who suffered brain tumors called meningioma after using Depo-Provera or Depo-SubQ Provera birth control shots.
We do the legal research by talking to lawyers and reviewing court documents to bring you the latest updates on Depo-Provera lawsuits.
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October 2024:
Monique Jones became one of the first women to file a Depo-Provera meningioma lawsuit against Pfizer and other defendants. According to our research of the complaint, Jones claimed Pfizer and the other defendants knew or should have known that Depo-Provera could contribute to the development of meningiomas. Despite this, defendants did not warn the public about the risk and as of the date of the lawsuit's filing, there is no warning on the birth control shot's label. Jones' doctors are unwilling to perform surgery and so she will continue to live with symptoms such as headaches, blurred vision and vertigo.
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August 2024:
Lawyers continue to investigate claims of meningioma after Depo-Provera use. According to our research, these cases are in the early stages and haven’t entered a discovery phase yet.
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March 2024:
A study found women injected with medroxyprogesterone acetate, the active ingredient and generic form of the Depo-Provera shot, had a 5.6-fold higher risk of developing meningioma. French researchers published their findings in the British Medical Journal (BMJ) in March 2024.
About 74 million women worldwide use Depo-Provera, also widely known as the birth control shot, according to BMJ study authors. Serious Depo-Provera side effects include significant bone density loss, slight increase in breast cancer risk and blood clots.
Earlier Depo-Provera lawsuits claimed Pfizer failed to warn the public about the risk of pseudotumor cerebri and bone density loss. Drugwwatch’s legal partners aren’t accepting cases for these injuries, and this page focuses on Depo-Provera brain tumor lawsuits.
Do I Qualify for a Depo-Provera Shot Lawsuit?
If you took Depo-Provera, Depo-SubQ Provera or a generic form of these birth control shots and were later diagnosed with meningioma, you may qualify for a Depo-Provera shot lawsuit.
To qualify for a lawsuit with our legal partners, you must meet specific criteria, including length of Depo-Provera use, number of times the shot was used and a specific injury diagnosis.
These are just guidelines, and you should contact a Depo-Provera lawyer for a free case evaluation to find out about your specific.
- Products: Brand name Depo-Provera, Depo-SubQ Provera or an authorized generic form of these birth control shots called medroxyprogesterone acetate
- Number of Uses: At least two times
- Time of Use: Any time after 1992
- Diagnosis: Meningioma after using Depo-Provera, Depo-SubQ Provera or a generic form of medroxyprogesterone acetate
Keep in mind that each state has a time limit to file a claim called the statute of limitations. Depending on the state you live in, you may not qualify based on state laws. Make sure you contact an attorney right away to preserve your legal right to file a claim.
“People are mostly suing Pfizer, the company that makes Depo-Provera. The lawsuits claim that Pfizer either knew or should have known that Depo-Provera could cause brain tumors but didn’t give users a proper heads-up. As a result, people who developed these tumors are taking legal action to hold the company responsible,” said Aron Solomon, JD, Chief Strategy Officer at Amplify, a legal marketing agency.
“People are mostly suing Pfizer, the company that makes Depo-Provera. The lawsuits claim that Pfizer either knew or should have known that Depo-Provera could cause brain tumors but didn’t give users a proper heads-up.”
Depo-Provera Lawsuit Case Study
Drugwatch has analyzed Depo-Provera cases, including this lawsuit filed by Monique Jones in California. This is an example of Depo-Provera lawsuits lawyers have been accepting. Keep in mind that each case is unique. Discussing your situation with a lawyer can help determine if you or your family qualify for a Depo-Provera lawsuit.
"Ms. Jones is seeking compensation for her injuries relating to the development of a cerebral meningioma which was caused by her usage of Depo-Provera," one of Jones' attorneys Brendan McDonough told Drugwatch. "We believe Pfizer and others knew for many years about the risk of developing meningioma associated with Depo-Provera."
Monique Jones filed her Depo-Provera lawsuit in October 2024 in the United States District Court Central District of California.
Depo-Provera Usage
Jones first started using Depo-Provera in 2000 at the age of 20. She received the birth control shot until September 2024. In total, she received about 91 injections.
Injuries Claimed
In the lawsuit, Jones claimed she suffered from symptoms such as lightheadedness, ear itching, headaches, vertigo and blurred vision. Ultimately, doctors diagnosed her with intracranial meningioma in 2020. Because of the location of the meningioma, doctors were unwilling to perform risky surgery to alleviate symptoms, and Jones continues to suffer from these symptoms.
Relief Sought
General damages for pain and suffering as well as loss of enjoyment of life, attorney’s fees and other damages.
Depo-Provera and Brain Tumors
According to a March 2024 study published in BMJ, Depo-Provera is linked to a higher risk of developing meningioma, a type of noncancerous brain tumor. Study authors found that Depo-Provera users had a 5.6-fold increase in the risk of developing meningioma with long-term use.
This risk increase was more than any other birth control method studied. However, since this was an observational study, researchers cannot say for sure that the shot causes meningioma.
“The [March 2024 study] recently published in BMJ is the first to assess the risk associated with progestogens that are much more widely used for multiple indications, such as contraception. This population-based study shows an association between the prolonged use of medrogestone (5 mg), medroxyprogesterone acetate injection (also called Depo-Provera) (150 mg), and promegestone (0.125, 0.25, 0.5 mg) and a risk of intracranial meningioma requiring surgery,” according to Drugwatch expert and oncology clinical pharmacy specialist, Dazhi Liu.
“This [BMJ] population-based study shows an association between the prolonged use of…medroxyprogesterone acetate injection (also called Depo-Provera) (150 mg)…and a risk of intracranial meningioma requiring surgery.”
The BMJ study led to lawyers investigating claims from women who took the birth control shot and later developed meningioma. The birth control shot has been on the market since the early 1990s and doesn’t have any warnings about developing brain tumors. Fortunately, meningiomas are not typically malignant, and the study didn’t find any malignant tumors in women who used Depo-Provera.
However, these tumors can affect nearby brain tissue, nerves and blood vessels and cause serious disability. When this happens, the tumor must be surgically removed, and brain surgery may have serious risks.
Pfizer told the Guardian, “We are aware of this potential risk associated with long-term use of progestogens and, in collaboration with regulatory agencies, are in the process of updating product labels and patient information leaflets with appropriate wording.”
Other Depo-Provera Lawsuits
In addition to the current litigation on Depo-Provera and brain tumors, plaintiffs have filed Depo-Provera lawsuits for pseudotumor cerebri and loss of bone mineral density.
Pseudotumor Cerebri Lawsuits
Plaintiffs filed lawsuits that claimed Depo-Provera could cause pseudotumor cerebri, a condition that occurs when pressure builds up in the brain, mimicking a tumor. Lawsuits claimed Pfizer didn’t warn the public about the risk.
Some women also filed Mirena lawsuits for this condition. There have been no publicly announced settlements or jury verdicts from Depo-Provera or Mirena litigation for this injury claim.
Bone Density Lawsuits
Some women also filed bone density lawsuits, however, there were no notable settlements or jury verdicts in the U.S. The lawsuits claimed Pfizer failed to warn that Depo-Provera could lower bone density that could lead to osteopenia and osteoporosis. In the U.S., Pfizer added a black box warning to Depo-Provera’s medication label in 2004.
Canadian women filed a class action against Pfizer in May 2008. The lawsuit claimed Pfizer misrepresented the risk of significant and potentially irreversible bone mineral density loss with Depo-Provera.
In September 2021, Pfizer paid $1,913,750 to the class and $262,500 to health insurance companies to settle these Canadian class action claims.
Finding a Depo-Provera Lawyer
When finding a Depo-Provera lawyer, we recommend seeking out a lawyer that has experience in handling pharmaceutical injury lawsuits and has a good track record of obtaining settlements and jury verdicts against large corporations. For example, Drugwatch’s partners have decades of experience taking on companies such as Johnson & Johnson, Bayer and Pfizer — the maker of Depo-Provera.
They have track records of negotiating settlements and winning jury verdicts on behalf of their clients. These firms have recovered billions on behalf of their clients, and they have the resources to fight these drug companies in court. They can also help guide you through the process.
“If you’re thinking about filing a lawsuit over Depo-Provera, there are a few things you should keep in mind. First, you’ll need to show that your use of the shot is linked to developing a meningioma, which usually involves gathering medical records and expert opinions.”
“If you’re thinking about filing a lawsuit over Depo-Provera, there are a few things you should keep in mind. First, you’ll need to show that your use of the shot is linked to developing a meningioma, which usually involves gathering medical records and expert opinions,” Solomon said.
You can get in touch with an experienced product liability lawyer by signing up for a free case evaluation on Drugwatch. After reviewing your contact form, our legal partners will get in touch with you to ask you a few questions about your Depo-Provera usage. Then, they will let you know if they can help.
Brendan McDonough, Esq. discusses Depo-Provera meningioma lawsuits, including what to expect when you contact an attorney to file a claim.
- Why are people filing Depo-Provera lawsuits?
Recent studies have shown that usage of Depo-Provera is associated with a significantly increased risk of developing cerebral meningioma.
- What are the injuries your clients are claiming in these cases?
The signature injury is cerebral meningioma, which is a tumor of the meningeal lining of the brain that can press on sensitive brain structures and cause severe problems including seizures, headaches, vision loss, and even death.
- What should people filing Depo-Provera lawsuits expect from a lawyer?
People should expect to provide their medical history, including their usage of Depo-Provera and any history of pregnancy and other hormonal contraceptive use, as well as diagnosis and treatment information related to their meningioma.
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