What Happened?
Depo-Provera (medroxyprogesterone acetate) is a hormonal birth control injection manufactured by Pfizer, administered every three months since the 1960s. A landmark 2023 BMJ study found that women who used Depo-Provera for at least one year had a 5.6-fold increased risk of meningioma (brain tumor). Pfizer and its predecessors were aware of studies linking progestin hormones to meningioma growth — including studies from the 1990s — and failed to adequately warn patients. The FDA updated the Depo-Provera label in 2024 to include a meningioma warning.
Who Qualifies?
You received Depo-Provera injections for birth control for at least 12 months (stronger cases for 3+ years of use). You have been diagnosed with a meningioma (intracranial or spinal) confirmed by MRI or surgical pathology.
Primary Diagnoses:
Litigation Status
No consolidated MDL established as of early 2025 — cases are being filed in state and federal courts. A motion for MDL consolidation is anticipated. The litigation is in early stages with high growth trajectory.
Estimated Compensation
Brain tumor cases requiring surgery are among the most serious personal injury cases. Expected range: $250,000-$2,000,000+ for cases requiring brain surgery. Duration of Depo-Provera use and severity of neurological deficits drive value.
Frequently Asked Questions
How long do I need to have used Depo-Provera to qualify?
Does the type of meningioma matter?
What records do I need?
I stopped Depo-Provera years ago — can I still file?
Is this the same as other birth control lawsuits?
Will filing affect my current healthcare?
Why is this considered high-value?
Can the estate of a deceased patient file?
Think You May Qualify?
Take a quick eligibility check or request a free review.
Filing Deadlines Apply
Statutes of limitations vary by state.
100% Free, No Obligation
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Gather Your Documents
Having these documents ready will help your attorney evaluate your case faster:
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