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Depo-Provera Lawsuit

Depo-Provera® lawsuits claim Pfizer failed to warn users of the risk of developing meningiomas (tumors near the brain) after prolonged use of this birth control shot.

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Case Overview

People are filing Depo-Provera lawsuits against Pfizer, the manufacturer of Depo-Provera. They claim that users weren’t properly warned that the birth control shot may cause women to develop meningiomas. A meningioma is a tumor that grows in the membrane surrounding the brain. Motley Rice attorneys are representing people filing Depo-Provera lawsuits.

Important Depo-Provera lawsuit updates

  • March 2026: The Depo-Provera MDL has grown to 3,099 lawsuits since its creation in 2025.
  • December 2025: The FDA required Pfizer to issue an update to the Depo-Provera Warning Label to notify users of the increased risk of meningiomas.
  • September 2025:  A new study found that Depo-Provera use is more likely to cause meningiomas than other contraceptive use or no contraceptive use. 

Key takeaways about Depo-Provera meningioma lawsuits

  • Women are filing Depo-Provera meningioma lawsuits. These women have developed dangerous tumors near the brain and spine. They claim the tumors potentially resulted from their use of the contraceptive shot.
  • Meningiomas are tumors that develop in the tissue covering the brain and spinal cord. Studies have found that long-term use of Depo-Provera may put users at an increased risk for meningiomas.
  • If you’ve experienced meningioma as a result of using the Depo-Provera birth control shot, you may be eligible to file a claim in the Depo-Provera MDL.

Why are people filing Depo-Provera lawsuits?

Users should be aware of the potential birth control risks and side effects of the contraceptives they use. People are filing Depo-Provera lawsuits after a March 2024 study linked the birth control shot to meningioma. This tumor forms in the meninges (membranes near the brain and spinal cord) and is often benign.

When a meningioma grows, it can affect brain tissue, nerves and blood vessels and may lead to severe disability. Those who file these product liability and personal injury lawsuits must already be diagnosed with meningioma by a medical professional. Motley Rice lawyers are not currently accepting cases for other injuries or harms associated with Depo-Provera.

Depo-Provera meningioma lawsuits are in their early stages. If you took this contraceptive shot and were diagnosed with a meningioma by a medical professional, you may qualify to file a birth control lawsuit in the Depo-Provera multidistrict litigation. The lawsuit docket is called In re: Depo-Provera (Depot Medroxyprogesterone Acetate) Products Liability Litigation, MDL No. 3140.

Studies link Depo-Provera shot to increased risk of meningioma

In September 2025, the medical journal JAMA Neurology released a study that found an increased risk of meningiomas associated with the Depo shot. This new study on Depo-Provera found that its users were more likely to develop meningiomas than women who used other contraceptives or no contraceptives.

An earlier 2025 study from the University of British Columbia also assessed the risk of developing a meningioma. The study compared 72,181 Depo-Provera users and 247,180 users of oral contraceptives that contain ethinylestradiol-levonorgestre (EE-LNG).

The study found that women who use Depo-Provera have a higher risk of developing meningioma brain tumors than those who use EE-LNG. Researchers stated, “The adjusted incident rate ratio (IRR) for meningioma for greater than one year of use was 3.55.”

A 2024 British Medical Journal (BMJ) study linked the use of injectable Depo-Provera to an increased risk of meningioma. The researchers looked at people who used Depo-Provera as their primary form of birth control. They concluded that people who used Depo-Provera for a year or more were five times more likely to develop a meningioma that required surgery.

What are meningiomas?

Meningiomas are a type of brain tumor that is usually non-malignant (not cancerous). These tumors originate in the tissue (meninges) covering the spinal cord and the brain. They are commonly found near the top and the outer curve of the brain but may also form at the base of the skull. They can spread to other parts of the central nervous system through cerebrospinal fluid. 

There are three grades of meningiomas: 

  • Grade 1: The most common meningiomas, which tend to grow slowly
  • Grade 2: Mid-grade meningiomas, with a higher risk of coming back if removed
  • Grade 3: Malignant, cancerous and fast-growing meningiomas, which are fairly rare

The symptoms of meningiomas often vary with where the tumor forms. Some potential symptoms include:

  • Confusion
  • Headaches (more severe in the morning)
  • Inability to hear or smell
  • Seizures
  • Vision issues

The risk of meningiomas was added to the Depo-Provera Warning Label in December 2025.

Contact a Depo-Provera lawsuit attorney

If you or a loved one used the Depo-Provera birth control shot and have a medical diagnosis of a meningioma, you may be eligible to file a lawsuit.

You can also reach our team by calling 1.800.768.4026.

To be eligible to file a claim against Depo-Provera for the meningioma harms experienced, individuals must have:

  • Used brand-name Depo-Provera, Depo-SubQ Provera or an authorized generic medroxyprogesterone acetate birth control shot. They must have followed the manufacturer’s directions and the doctor’s recommendations
  • Used Depo-Provera as a primary form of birth control more than twice
  • Used Depo-Provera for one year or more (for cases involving meningioma)
  • Used Depo-Provera any time after its FDA approval in 1992
  • Suffered severe health effects, including meningioma, related to the use of Depo-Provera

To document injuries, you’ll need evidence such as medical records and billings that detail your Depo-Provera use and the associated costs. An attorney with experience in medical drug lawsuits can help determine your eligibility, gather the proper evidence and build your case.

What is Depo-Provera?

Depo-Provera is the brand name for medroxyprogesterone acetate (MPA). It’s an injectable form of birth control made by Pfizer. It works by blocking the release of an egg from the ovaries during the reproductive cycle (ovulation). Depo-Provera also thickens the cervical mucus to stop sperm from reaching the egg in case ovulation occurs.

People who use Depo-Provera receive a shot — commonly called the Depo shot or birth control shot — on a routine schedule every three months. A doctor injects the medication into the patient’s arm or buttocks. Depo-Provera contains a progesterone hormone that can protect against pregnancy for up to 14 weeks. The shots are usually given every 12 weeks.

Depo-Provera long-term side effects

There are many side effects associated with birth control. These side effects can vary depending on the dose, the individual’s reaction to the drug, the type of birth control medication used and how long the medication is taken.

Some common Depo-Provera side effects may include:

  • Acne
  • Bloating
  • Dizziness
  • Fatigue
  • Headaches
  • Menstruation changes
  • Nausea
  • Stomach pain
  • Weight gain

Other serious side effects of Depo-Provera may include:

  • Blood clots
  • Heart attack
  • Risk of developing certain cancers
  • Seizures
  • Stroke

Depo-Provera users may experience long-term side effects, including:

  • Bone density loss: Depo-Provera also has a warning for loss of bone mineral density (BMD) or bone density loss after long-term use. Bone density loss can lead to serious fractures and even irreversible damage. This warning reads, “Women who use Depo-Provera Contraceptive Injection (Depo-Provera CI) may lose significant bone mineral density. Bone loss is greater with increasing duration of use and may not be completely reversible.” This boxed warning also suggests using Depo-Provera no longer than two years.
  • Meningioma: Studies have shown that Depo-Provera users may have a higher risk of developing meningioma brain tumors after using the contraceptive long-term over several years. These tumors are serious and could lead to surgery and other side effects.

Depo-Provera lawsuit settlements

This litigation is in its early stages and few cases have been settled. The Depo-Provera Products Liability Litigation MDL was only recently created. As the litigation continues to progress, Depo-Provera lawsuit settlement conversations could take place.

It’s important to note that lawsuit settlement amounts in pharmaceutical medicine cases like these can vary significantly. Factors such as the severity of the diagnosed meningioma, the medical evidence provided and the timing of the medical diagnosis will all influence the compensation outcome. Individuals considering legal action should talk with an attorney who has experience with medical drug and device litigation. They can help determine potential compensation or payout amounts based on the specific situation.

Types of damages available in Depo-Provera lawsuits

In Depo-Provera lawsuits, a meningioma is the “injury.” People (plaintiffs) filing birth control lawsuits may be eligible to seek damages for:

  • Healthcare costs associated with injuries caused by Depo-Provera use
  • Lost wages for time missed from work due to injury-related health issues
  • Pain and suffering
  • Wrongful death of a loved one (if applicable)

The court or jury may also award additional damages to the injured party in extreme cases. This action could occur to punish or force changes in business practices of the defendant.

These “punitive damages” can be awarded if a court determines that the defendant’s actions were intentional and/or outrageous under the law. While no award is guaranteed, a lawyer can help explain the damages you might be able to obtain in a Depo-Provera lawsuit.

Depo-Provera lawsuit news and recent updates

03.02.26

New lawsuits added to the Depo-Provera MDL

As of the beginning of March, the Depo-Provera MDL had grown to 3,099 pending actions.

01.05.26

Nearly 2,000 Depo-Provera lawsuits by the beginning of 2026

The U.S. Judicial Panel of Multidistrict Litigation reported that 1,752 cases were pending in the Depo-Provera MDL at the beginning of the year.
 

12.17.25

New Depo-Provera warning label issued by FDA

The Depo-Provera warning label informed users about the potential to cause meningiomas. The label advised doctors to monitor patients for signs or symptoms of the tumor and discontinue use of the drug if the patient is diagnosed with the condition. 
 

09.03.25

New study shows association between Depo shot and meningioma risk

JAMA Neurology published a study online that looked at the risk of developing meningiomas. In the study, only the use of depot medroxyprogesterone acetate was associated with an increased risk of developing meningiomas. Depot medroxyprogesterone acetate is the active ingredient in Depo-Provera. Other contraceptives, including oral medroxyprogesterone acetate, didn’t show an increased risk of meningiomas.
 

06.02.25

June report shows MDL growth

There were 348 pending actions in the Depo-Provera Products Liability Litigation, MDL No. 3140.

05.12.25

MDL judge addressed deficiencies in complaints

MDL Judge Rodgers issued an order to create a process for what specific allegations should be included in plaintiffs Depo-Provera complaints. This included a meningioma physical injury and a clear injury that resulted from a Depo-Provera product.

05.01.25

MDL numbers increased leading into May

The MDL report showed 289 pending actions as of May 1, 2025.

04.01.25

April report showed rise in MDL numbers

The Depo-Provera MDL grew to 130 pending actions.

03.03.25

Depo-Provera MDL started to grow

After around one month of the MDL being established, there were 78 pending actions in the Depo-Provera MDL No. 3140.

02.07.25

MDL Established

MDL No. 3140, In re: Depo−Provera (Depot Medroxyprogesterone Acetate) Products Liability Litigation was established in the District Court for the Northern District of Florida on February 7, 2025 before Judge Rodgers. Judge Rodgers has since approved various case management orders governing the litigation and appointed plaintiff leadership positions, including Motley Rice attorney Carmen Scott’s appointment to the Plaintiffs’ Steering Committee.

02.02.25

Study showed increased meningioma risk

University of British Columbia researchers studied the risk of developing meningioma in women who used Depo-Provera versus women who used oral contraceptives. They found the risk of developing meningioma was 3.55 higher for Depo-Provera users compared to women who used other oral birth control.

10.24.24

New meningioma lawsuit filed in California

On October 24, 2024, a woman filed a new Depo-Provera meningioma lawsuit in California. Her lawsuit against Pfizer claims the company didn’t warn consumers of the potential for meningioma. It also highlights that the U.S. warning labels still don’t mention the increased risk of brain tumors, even though the European Union and United Kingdom labels do.

10.10.24

Pfizer’s Irish arm released meningioma warning

On October 10, 2024 Pfizer Healthcare Ireland released a meningioma warning approved by the Irish Health Products Regulatory Agency. The warning discusses “increased risk of developing meningioma with high doses of medroxyprogesterone acetate … primarily after prolonged use (several years).” It was issued to Irish healthcare professionals.

On July 11, 2024, Pfizer updated its label for Depo-Provera in the United States, but the update did not include mentions of meningioma. No similar warnings have been issued from the U.S. arms of Pfizer to the FDA, U.S. consumer product agencies or U.S. medical professionals.

10.01.24

New Depo-Provera meningioma lawsuit filed

On October 1, a woman who had used Depo-Provera for approximately 17 years filed the first Depo-Provera meningioma lawsuit. In 2022, she had been diagnosed with a Grade 1 and a Grade 2 meningioma tumor. Her lawsuit claims that Pfizer knew or should have known that the birth control injections could cause brain tumors.

05.01.24

Pfizer updates European labeling

Pfizer updated Depo-Provera’s Patient Information Leaflet (PIL) in Europe to include information about meningioma under the “Warnings and precautions” section. However, no such info was given to U.S. doctors and consumers.

03.01.24

New study connects Depo-Provera to meningioma risk

The British Medical Journal (BMJ) released a new study identifying the possibility of an increased risk for meningioma among Depo-Provera users. 

06.01.22

New study connects progestogen medications to meningioma

The European Journal of Neurology published a study concluding that long-term exposure to medications containing higher doses of progestogen potentially increased the risk of developing meningioma.

09.01.21

Pfizer settles Canadian bone density class action

Pfizer settled the Depo-Provera bone density loss class action lawsuit, agreeing to pay $1,913,750 to the class members (people harmed) and $262,500 to health insurers.

05.01.08

Bone density class action lawsuit filed in Canada

The Canadian class action against Pfizer for bone mineral density loss was authorized.

View Full Timeline

Frequently asked questions about the Depo shot lawsuit

Does Depo-Provera cause brain tumors?

Studies have shown a direct link between long-term Depo-Provera shot birth control use and an increased risk of developing meningioma tumors. Women who use the contraceptive for over a year should be aware of this potential risk and discuss any signs of meningiomas with their doctor.

Is there a Depo-Provera class action lawsuit?

No. As of June 2025, there is no active class action lawsuit against Depo-Provera for causing meningioma brain tumors. But hundreds of individual lawsuits have been filed into the Depo-Provera Products Liability MDL.

A previous class action lawsuit for Depo-Provera was filed in Canada. This lawsuit concerned the shot’s connection to bone mineral density loss. The suit was settled in 2021.

Am I eligible to file a Depo-Provera lawsuit claim?

People diagnosed with meningioma after using Depo-Provera may be eligible to file a Depo-Provera lawsuit. We are not currently accepting claims for other injuries. You must have a diagnosed meningioma as a result of Depo-Provera use to file a lawsuit.

You can contact Motley Rice to learn more, find out if you qualify for a lawsuit and discuss the time limit for claims.

Don’t delay — a statute of limitations may limit your ability to file based on a timeline set in your jurisdiction.

How much can I receive in Depo-Provera lawsuit compensation?

The compensation amount plaintiffs can receive in a successful Depo-Provera lawsuit may vary. It depends on various factors, including the severity of the medical diagnosis and the evidence provided in the case. Medical costs associated with the diagnosis, lost wages, pain and suffering and other unique facts of the claim are also considered.

While there are no guarantees that a lawsuit will be successful, it is recommended that you consult with an attorney as soon as possible.

Our experience with women’s health litigation

The medical attorneys at Motley Rice have represented thousands of women injured by prescription and over-the-counter medications and medical devices, including birth control medications like Depo-Provera and Paragard IUD.

If you believe a prescribed birth control product may have injured you or a loved one, the legal professionals at Motley Rice have the resources to investigate and help you:

  • Identify the potentially harmful medication
  • Investigate whether it harmed you
  • Review the manufacturer’s regulatory compliance
  • Examine the manufacturer’s instructions regarding use and warnings about side effects
  • Review other issues that could affect your claim

Read more on our women’s health litigation.


Do not stop taking a prescribed medication without first consulting with your doctor. Discontinuing a prescribed medication without your doctor’s advice can result in injury or death. Depo-Provera and Paragard remain approved by the U.S. Food and Drug Administration.

What is Depo-Provera?

Why are people filing Depo-Provera lawsuits?

Studies link Depo-Provera shot to increased risk of meningioma

Depo-Provera brain tumor lawsuit eligibility

Depo-Provera long-term side effects

Depo-Provera lawsuit settlements

Depo-Provera lawsuit news and recent updates

Frequently asked questions about the Depo shot lawsuit

Our experience with women’s health litigation

About the Author

Sources
  1. BMJ Group. Prolonged use of certain hormone drugs linked to increased brain tumor risk.
  2. Cleveland Clinic. Depo-Provera® (Birth Control Shot).
  3. Frey C., Sodhi M., Fatehi M., Kezouh A., Etminan M. Use of Medroxyprogesterone Acetate and Risk of Meningiomas: A Comparative Safety Study. ResearchGate. 2025 Feb.
  4. GoodRx. 10 Depo-Provera Side Effects to Consider: Weight Gain, Headaches, and More.
  5. HarrisMartin. Another Calif. Federal Lawsuit Alleges Link Between Brain Tumors, Depo-Provera.
  6. Healthline. Depo-Provera: Everything to Know About the Birth Control Shot.
  7. Hoisnard L, Laanani M, Passeri T, Duranteau L, Coste J, Zureik M, Froelich S, Weill A. Risk of intracranial meningioma with three potent progestogens: A population‐based case-control study. European Journal of Neurology. 2022 Jun 20;29(9):2801–2809.
  8. Lawyer Monthly. Depo-Provera Lawsuits Allege Link to Brain Cancer.
  9. Mayo Clinic. Depo-Provera (contraceptive injection).
  10. Mayo Clinic. Meningioma.
  11. National Cancer Institute. Meningioma: Diagnosis and Treatment.
  12. Pfizer. DEPO-PROVERA® CI.
  13. Pfizer. Package leaflet: Information for the patient. Depo-Provera 150 mg/ml.
  14. Pfizer Healthcare Ireland. IMPORTANT MEDICINE SAFETY INFORMATION: Medroxyprogesterone acetate: Risk of meningioma and measures to minimise this risk.
  15. Roland N, Neumann A, Hoisnard L, Duranteau L, Froelich S, Zureik M, Weill A. Use of progestogens and the risk of intracranial meningioma: national case-control study. BMJ. 2024;384:e078078.
  16. UNITED STATES DISTRICT COURT NORTHERN DISTRICT OF FLORIDA PENSACOLA DIVISION. IN RE: DEPO-PROVERA (DEPOT MEDROXYPROGESTERONE ACETATE) PRODUCTS LIABILITY LITIGATION.
  17. United States Judicial Panel on Multidistrict Litigation. Notice Of Hearing Session.
  18. U.S. Food and Drug Administration. Depo-Provera CI.
  19. U.S. Judicial Panel on Multidistrict Litigation. Pending MDLs.
  20. Xiao T, Kumar P, Lobbous M, Yogi-Morren D, Soni P, Recinos PF, et al. Depot medroxyprogesterone acetate and risk of meningioma in the US. JAMA Neurology. September 2025; 82(11):1094-1102.
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