Depo-Provera Settlement Calculator 2026: What Real Depo-Provera Cases Have Paid
Use the Depo-Provera settlement calculator to organize potential claim factors after repeated Depo-Provera or depot medroxyprogesterone acetate injections and a later meningioma diagnosis, including injection history, treatment, neurological effects, medical records, wage loss and other damages.
- Organizes Depo-Provera injection history and diagnosis timing.
- Captures surgery, radiation, surveillance and neurological effects.
- Helps identify missing medical, pharmacy, wage and damages records.
- Separates official litigation and medical facts from commentary.
Get Your Free Depo-Provera Case Report
Answer the guided questions using your injection history, diagnosis, treatment, neurological symptoms, medical expenses and other documented losses.
Key Facts About Depo-Provera Meningioma Claims
Federal Depo-Provera products-liability cases are centralized in MDL No. 3140 before Judge M. Casey Rodgers in the Northern District of Florida. The JPML report dated September 1, 2026 lists 6,403 actions pending and 6,510 historical actions in the MDL.
Active Federal MDL
MDL 3140 coordinates common pretrial issues while individual plaintiffs retain individual claims and damages issues.
Official court page →6,403 Pending Actions
The September 1, 2026 JPML actions-pending report lists 6,403 actions in MDL 3140.
Official JPML reports →FDA Meningioma Warning
The current FDA-approved prescribing information states that meningioma cases have been reported following repeated administration, primarily with long-term use.
FDA prescribing information →Research Continues
Multiple observational studies have reported an association between injectable medroxyprogesterone acetate and meningioma risk, particularly with longer exposure.
Review study context →Who May Qualify for a Depo-Provera Lawsuit Review?
Eligibility is not determined by this page. Attorneys evaluating a potential claim may review the type and duration of medroxyprogesterone acetate injections, diagnosis timing, tumor type and location, treatment, medical proof, alternative risk factors, damages, defendants and applicable filing deadline.
Factors That May Support Review
- Documented Depo-Provera or depot medroxyprogesterone acetate injections before diagnosis
- Confirmed intracranial meningioma diagnosis supported by imaging or pathology
- Longer or repeated injection history documented in pharmacy, clinic or insurance records
- Surgery, radiation, neurological symptoms, surveillance or future-care needs
- Documented medical costs, wage loss, disability or quality-of-life impact
Issues Requiring Closer Review
- Unclear injection dates or product identity
- Diagnosis before use began
- Tumor type not clearly documented as an intracranial meningioma
- Missing imaging, pathology, pharmacy or provider records
- Statute-of-limitations, jurisdiction or other deadline concerns
What Depo-Provera Cases Have Actually Produced
No Depo-Provera meningioma case has produced a public verdict, and no settlement amount has been disclosed. Here is what is actually on the record as of September 2026.
Pfizer master settlement agreement
Not disclosedSigned 21 July 2026, covering a majority of the cases already on file in the MDL and in New York state court. The parties estimate roughly 80% of MDL plaintiffs will be eligible.
Private agreement. No amount has ever been made public.MDL 3140, Northern District of Florida
6,403 casesPending before Judge M. Casey Rodgers on 1 September 2026. No Depo-Provera case has been tried to a verdict.
Source: JPML pending MDL report, 1 September 2026.Registration and payment
Q1 2027The court has said settlement registration should be completed in November 2026, and the parties expect payments to begin in the first quarter of 2027.
Registration is open only to claimants whose cases were already on file.What the 2026 Depo-Provera Master Settlement Actually Is
A master settlement agreement is not a payout schedule, and the difference decides what this page can honestly tell you. Pfizer and plaintiffs’ leadership announced a global agreement in principle on June 15, 2026, and Judge M. Casey Rodgers vacated the first bellwether trial, Toney v. Pfizer, which had been set for December 7, 2026. The master agreement itself was signed on July 21, 2026 and covers most of the federal claims then on file in MDL 3140, with the parties estimating that roughly 80 percent of MDL plaintiffs will meet the eligibility criteria. BrownGreer PLC was appointed settlement administrator on August 5, 2026. Every one of those steps is real, dated and checkable — and not one of them is a dollar figure.
The terms of the agreement are confidential. There is no public payout chart, no per-tier compensation range and no total fund size confirmed by the court or by either party. That is an ordinary feature of a private aggregate settlement: the parties negotiate a framework, a third-party administrator evaluates each claim against agreed criteria, and individual offers go to individual claimants rather than to the docket. It also means that any specific Depo-Provera settlement amount circulating online right now — and several are circulating, usually as a range spanning an order of magnitude — has no basis in any filed document. This page does not repeat them, and a reader who finds one elsewhere is entitled to ask which record it came from.
What the settlement does not do matters as much as what it does. The court noted that the agreement will not end the MDL: only plaintiffs who meet the eligibility criteria agreed by the parties will have the opportunity to resolve their claims, so a claim that falls outside those criteria stays in litigation on the ordinary track. Pfizer’s federal preemption motion was still undecided when the agreement was reached, which is unusually early in a pharmaceutical MDL and is part of why the terms carry the conditions they do. Registration for the programme is expected to open and complete during November 2026, with the first payments projected for the first quarter of 2027 — projected by the administrator’s timetable, not guaranteed by any order.
For a claimant, the practical work is the same as it was before the agreement: the injection records establishing how long Depo-Provera or its generic equivalent was used, the imaging and pathology confirming an intracranial meningioma, and the dates linking the two. Those are the documents an administrator evaluates, and they are what the calculator on this page organises. Our Depo-Provera lawsuit guide covers who may qualify and on what theories, the Depo-Provera settlement amounts page records the money question as it develops, and our 2026 settlement update tracks each filing as it lands.
Depo-Provera, Medroxyprogesterone Acetate & Meningioma Research
The medical literature has developed quickly. The studies below are observational and should be read as population-level evidence rather than a diagnosis or individual causation determination.
BMJ 2024 National Case-Control Study
A French national case-control study reported an odds ratio of 5.55 for injectable medroxyprogesterone acetate and intracranial meningioma requiring surgery; the excess risk was driven by prolonged use of at least one year.
PubMed study record →U.S. Population Study
A U.S. retrospective cohort study reported a relative risk of 2.43 for meningioma diagnosis among depot medroxyprogesterone acetate users compared with controls, with higher-risk patterns tied to longer exposure.
PubMed study record →2026 Danish Population Study
A Danish case-control study reported an odds ratio of 4.55 for injectable medroxyprogesterone and incident meningioma, adding another population-level dataset to the evidence base.
PubMed study record →Evidence That Can Strengthen a Depo-Provera Claim Review
The calculator is most useful when answers can be tied to records rather than estimates from memory.
- Depo-Provera injection records and dates
- Pharmacy, OB-GYN, clinic or insurer records confirming use
- MRI or CT imaging confirming the meningioma
- Pathology, neurology, oncology or neurosurgery records
- Craniotomy, radiation and hospitalization records
- Records of seizures, vision loss, hearing changes, headaches or cognitive effects
- Medical bills and out-of-pocket expenses
- Lost-income and employment documentation
- Disability, caregiving and rehabilitation records
- Future-treatment or surveillance recommendations
- A dated injection-to-diagnosis timeline
- Documents showing the impact on normal activities and work
MDL No. 3140: Depo-Provera Litigation Status
MDL 3140 is pending in the Northern District of Florida before Judge M. Casey Rodgers. Multidistrict litigation coordinates common pretrial matters such as discovery and expert issues; it is not a class action and does not create a guaranteed settlement.
What Can Affect Depo-Provera Settlement Value?
1. Injection History
Duration, frequency, dose records and reliable proof of use can affect exposure analysis.
2. Tumor Characteristics
Location, size, recurrence, grade, symptoms and medical prognosis can affect treatment burden and damages.
3. Surgery & Treatment
Craniotomy, radiation, hospitalization, rehabilitation, surveillance and future care can materially affect losses.
4. Neurological Effects
Vision, hearing, seizure, balance, cognitive and other documented neurological limitations may affect damages.
5. Economic Loss
Medical expenses, wage loss, reduced earning capacity, disability and caregiving costs can increase documented damages.
6. Legal & Evidentiary Risk
Causation rulings, expert evidence, jurisdiction, deadlines, defendants and competing explanations can affect settlement posture.
How the Depo-Provera Settlement Calculator Works
The calculator organizes claim information into a preliminary educational model. It does not use one universal multiplier or substitute for medical, legal or records review.
1. Document Product Use
Enter injection duration and the strongest available records showing Depo-Provera or medroxyprogesterone acetate use before diagnosis.
2. Enter Diagnosis & Treatment
Use imaging, pathology, surgery, radiation, surveillance and neurological information whenever available.
3. Add Damages
Include medical expenses, wage loss, disability, future care, treatment burden and other documented losses.
Depo-Provera Lawsuit Filing Deadlines
There is no single national statute of limitations for every Depo-Provera claim. Deadlines can depend on state law, diagnosis date, discovery rules, prior proceedings, defendant-specific issues and other facts.
Related Depo-Provera & Settlement Resources
Depo-Provera Settlement Calculator FAQ
What does this tool actually give me?
It organizes product use, meningioma diagnosis, treatment, neurological effects and damages into an educational claim-value range. It does not predict an actual settlement.
What is the average Depo-Provera settlement amount?
No reliable universal average applies to an individual claim. The master settlement agreement signed on July 21, 2026 is confidential, so no court-approved payout schedule is public and any figure circulating online is unsupported by the record.
How many Depo-Provera cases are currently pending in MDL 3140?
The JPML report dated September 1, 2026 lists 6,403 actions pending. The count can change as actions are filed, transferred, dismissed or otherwise resolved.
Does the FDA label mention meningioma?
Yes. The prescribing information revised in December 2025 includes a meningioma warning and says cases have been reported after repeated administration, primarily with long-term use.
Does research prove Depo-Provera caused my tumor?
No population study can make that individual determination by itself. Medical causation requires claim-specific medical and legal analysis.
Does using the calculator create an attorney-client relationship?
No. Using this website or calculator does not create an attorney-client relationship. Representation requires acceptance by a licensed attorney and an engagement agreement.
Request a Free Depo-Provera Case Review
If you were diagnosed with a meningioma after Depo-Provera use, use the calculator to organize your records or request a confidential screening.
How We Sourced This Page
Every fact on this page is dated to the event that produced it. The June 15, 2026 agreement in principle and the vacatur of the Toney bellwether come from Judge Rodgers’s order in MDL 3140; the July 21, 2026 master settlement agreement, the roughly 80 percent eligibility estimate and BrownGreer’s August 5, 2026 appointment as administrator come from the reporting of that docket. The pending-case count comes from the Judicial Panel on Multidistrict Litigation’s own September 1, 2026 statistics report. Where the page describes what the medical literature shows about medroxyprogesterone acetate and intracranial meningioma, it links the peer-reviewed study rather than a summary of it, and where it describes the label, it links the FDA record.
This page publishes no settlement range, no average and no claim tier for Depo-Provera, because the master settlement agreement is confidential and no payout schedule has been filed or released. Ranges quoted elsewhere are attorney estimates, and an estimate offered before an administrator has evaluated a single claim is a guess with a dollar sign in front of it. Where this page states that something is projected — the November 2026 registration window, the first-quarter 2027 payment timetable — it says who is projecting it. Facts were re-read against their sources on September 12, 2026. The same standard governs the other TortAdvisor settlement calculators and the settlement amounts library.
Depo-Provera Litigation, FDA & Medical Sources
Northern District of Florida — MDL 3140
Official litigation page with current hearing dates, court documents and master-docket information.
Open official court page →JPML — September 1, 2026 Report
Official monthly report listing 6,403 actions pending in MDL 3140.
Open JPML pending-MDL reports →FDA — Depo-Provera CI Prescribing Information
Current federal labeling revised December 2025, including the meningioma warning and monitoring/discontinuation language.
Open FDA prescribing information →BMJ / PubMed — 2024 Study
French national case-control study evaluating selected progestogens and intracranial meningioma requiring surgery.
Open PubMed record →U.S. Medroxyprogesterone Study
U.S. population-based research examining depot medroxyprogesterone acetate and subsequent meningioma diagnosis.
Open PubMed record →2026 Danish Contraceptive Study
Population-level case-control research evaluating contraceptive progestogens and incident meningioma.
Open PubMed record →
