What Is a Depo-Provera Meningioma?
A meningioma is a tumor arising from the meninges — the protective membranes surrounding the brain and spinal cord. Depo-Provera's active ingredient (medroxyprogesterone acetate) is a synthetic progestin that binds to progesterone receptors on meningioma cells, stimulating tumor growth. Meningiomas express progesterone receptors at rates of 60–80%, making them uniquely vulnerable to synthetic progestin stimulation.
Meningioma Risk by Duration of Use
The risk increases with cumulative Depo-Provera exposure: ≤1 year use: 23% increased risk; 1–3 years: 150% increased risk (OR 2.50); >3 years: up to 460% increased risk (OR 5.6 in the French BMJ study). This dose-response relationship is critical evidence in the litigation because it demonstrates a causal mechanism rather than a coincidental association.
Meningioma Types and Grades
WHO Grade I meningiomas (80%) are slow-growing and typically benign but can still cause serious symptoms requiring surgical intervention. WHO Grade II (atypical, 15–20%) are more aggressive with higher recurrence rates. WHO Grade III (malignant, 1–3%) are cancerous and carry the most severe prognosis. All grades are included in the litigation.
Treatment Options
Treatment depends on tumor size, location, and grade. Options include: craniotomy (surgical removal), stereotactic radiosurgery (Gamma Knife), radiation therapy, and active surveillance with serial MRI imaging. Many patients require ongoing neurological monitoring even after successful surgery due to recurrence risk.
Scientific Evidence
Medroxyprogesterone Acetate and Meningioma: A Global Issue
Roland N, Froelich S, Weill A (2025). Frontiers in Global Womens Health
View on PubMed→Use of High-Dose Medroxyprogesterone Acetate and Risk of Intracranial Meningioma
Roland N, Neumann A, Hoisnard L, Gagne JJ, Froelich S, Weill A (2024). The BMJ
View on PubMed→The Association between Medroxyprogesterone Acetate Exposure and Meningioma
Griffin BR et al. (2024). Cancers
View on PubMed→Frequently Asked Questions
Related Pages
Depo-Provera Brain Tumor Symptoms
Meningioma symptoms develop gradually and include persistent headaches, vision changes, seizures, and cognitive decline. If you used Depo-Provera and experience these symptoms, request brain imaging from your doctor.
Depo-Provera Long-Term Use Risks
Long-term Depo-Provera use carries multiple serious risks: meningioma brain tumors (up to 5.6x risk), significant bone density loss (black box warning), weight gain, depression, and delayed return to fertility. The FDA recommends limiting use to 2 years.
Depo-Provera Settlement Amounts
No Depo-Provera meningioma cases have settled or gone to trial yet. Projected settlements based on comparable pharmaceutical brain injury litigation suggest $75,000 to $1.5 million+ depending on injury severity.
Pfizer Depo-Provera Lawsuit
Pfizer inherited Depo-Provera when it acquired Pharmacia & Upjohn in 2002. Despite international warnings dating to 2015, Pfizer did not add a U.S. meningioma warning until December 2025. Plaintiffs allege a pattern of delayed safety action prioritizing revenue over patient safety.
Depo-Provera Alternatives After Diagnosis
If you are diagnosed with a meningioma, the FDA recommends discontinuing Depo-Provera immediately. Safer contraceptive alternatives exist that do not carry meningioma risk, including copper IUDs, barrier methods, and non-progestin options.
Depo-Provera Military Veterans
Military women were disproportionately prescribed Depo-Provera due to its convenience for deployment. If you received Depo-Provera during military service and were later diagnosed with a meningioma, you may be eligible for both civil lawsuit compensation and VA benefits.
Depo-Provera MRI Screening
Current guidelines do not recommend routine MRI screening for asymptomatic Depo-Provera users. However, the updated FDA label instructs providers to monitor for meningioma symptoms. If you have symptoms, request brain imaging immediately.
Depo-Provera Brain Tumor Lawsuits Lawsuit
Depo-Provera (medroxyprogesterone acetate / MPA) is a contraceptive injection administered every three months. Over 2,000 lawsuits consolidated in MDL 3140 in the Northern District of Florida allege that Pfizer failed to warn about a significantly elevated risk of meningioma — a tumor in the tissue surrounding the brain and spinal cord. Women who received the shot for more than one year face up to a 5.6-fold increased risk, and the risk escalates with duration of use.
View full case overview