Developed a Brain Tumor? Get the Justice You Deserve
New research reveals a 5.6x increased risk
of brain tumors from Depo-Provera use
Over 435 federal cases filed • $150K-$1M+ projected settlements
$150K - $1M+ Settlements
Expert attorneys project substantial compensation based on case severity and precedent
No Fee Unless We Win
100% contingency basis - we cover all costs during litigation
Expert Legal Team
Specialized pharmaceutical litigation attorneys with proven track record
Free consultation • No obligation • Completely confidential

The Science Behind Depo-Provera Brain Tumor Claims
Groundbreaking research reveals a significant connection between this widely-used contraceptive injection and increased brain tumor risk.
2024 BMJ Study Findings
Published in the British Medical Journal, this landmark study analyzed over 100,000 women
Higher risk of developing intracranial meningioma
Comprehensive analysis from French healthcare data
Risk increases with longer duration of use
About Depo-Provera
Long-acting contraceptive injection containing medroxyprogesterone acetate
Primary Medical Uses
Associated Health Risks
Documented conditions linked to Depo-Provera use
Reported Conditions
Defendants in Litigation
Major pharmaceutical companies facing lawsuits for failure to warn about brain tumor risks
Federal Lawsuits Filed
Projected settlements range from $150,000 to $1,000,000+ based on case severity and legal precedent
Free consultation • No upfront fees • Completely confidential
International Recognition of Depo-Provera Dangers
Health authorities worldwide have acknowledged the serious risks, while U.S. women remain inadequately warned
FDA Black Box Warning
Since 2004
"Women who use Depo-Provera may lose significant bone mineral density..."
Critical Gap: FDA label still lacks brain tumor warnings that exist internationally.
Canadian Settlement
$2.176 Million (2021)
Pfizer settled bone density claims:
Note: Pre-dates 2024 brain tumor study
Global Warnings
EU, UK & Canada
Why not the U.S.?
Judge M. Casey Rodgers
Presiding over the Depo-Provera MDL • Previously delivered $6 billion 3M settlement
Proven track record
Accelerated timeline
Critical hearing date
⚠️ Critical September 2025 Deadline
Filing before Pfizer's preemption hearing is essential to preserve your claim
Frequently Asked
Questions
Get clear answers about Depo-Provera lawsuits and understand your legal options
Legal experts project compensation ranges based on case severity:
- High-Value Cases: $500,000 - $1,000,000+ (Grade II/III tumors, multiple surgeries, permanent damage)
- Mid-Tier Cases: $200,000 - $500,000 (Grade I tumors requiring surgery, significant complications)
- Conservative Cases: $150,000 - $300,000 (minimal treatment required, no permanent damage)
For comparison: Bayer paid $2.04 billion for 10,300 Yaz blood clot claims (avg. $198K) and $1.6 billion for 39,000 Essure claims. Given brain tumor severity and Pfizer's $150+ billion company value, Depo-Provera settlements could be substantial.
Nothing upfront. We work on a contingency fee basis, which means:
- No attorney fees unless we win your case
- No out-of-pocket expenses for investigation or filing
- We cover all case costs during litigation
- Our fee is a percentage of your settlement (typically 33-40%)
Timeline varies, but Judge Rodgers is known for moving cases quickly:
- Case Development: 2-6 months (initial filing and documentation)
- MDL Discovery: 6-18 months (evidence gathering phase)
- Settlement/Trial: Late 2026 - Early 2027 (bellwether trials expected)
Judge M. Casey Rodgers, who oversaw the $6 billion 3M earplug settlement, is aggressively pushing these cases. Settlement negotiations could begin much sooner than typical pharmaceutical litigation due to the rapid case growth (25% monthly) and strong scientific evidence.
The MDL requires specific documentation:
- Medical: Brain tumor diagnosis, pathology reports, surgical records, MRI/CT imaging studies
- Usage: Medical records confirming Depo-Provera injections (at least 2 injections), pharmacy records
- Timeline: Proof that meningioma diagnosis occurred after Depo-Provera use began
- Questionnaire: Completed "Plaintiff Proof of Use/Injury Questionnaire" within 120 days
Don't worry if you're missing documents - our legal team can help obtain necessary medical records through court-authorized discovery processes.
Yes, time limits apply and vary by state. Generally:
- Personal injury: 2-3 years from brain tumor diagnosis or discovery
- Wrongful death: 2-3 years from death
- Discovery rule: Clock may start when connection to Depo-Provera is discovered
Critical: With bellwether trials approaching in 2025, now is the time to file. Contact us immediately to ensure you don't miss your deadline.
You may qualify if you have:
- Qualifying diagnosis: Meningioma (brain tumor), intracranial tumor requiring surgery, or other brain-related complications
- Depo-Provera use: Received at least two injections of Depo-Provera or Depo-SubQ for contraception or medical treatment
- Timeline: Brain tumor diagnosis occurred after starting Depo-Provera treatment
Family members can also file wrongful death claims for deceased relatives who meet these criteria.
Depo-Provera litigation is rapidly progressing:
- Over 435 active lawsuits in MDL 3140 (Northern District of Florida) under Judge M. Casey Rodgers
- Key dates: September 29, 2025 hearing on Pfizer's federal preemption motion
- Discovery deadlines: July 25, 2025 for preemption issues; September 23, 2025 for general causation
- Explosive growth: From 78 cases in March to 435+ by July 2025
- Scientific basis: 2024 BMJ study showing 5.6x increased meningioma risk
With international warning labels already in place in EU/UK/Canada, pressure is mounting for U.S. settlements before bellwether trials.
The Depo-Provera litigation has several powerful advantages:
- Failure to Warn: Pfizer provides meningioma warnings in EU/UK/Canada but not the U.S.
- Long-term Knowledge: Scientific literature from 1983 established the progesterone-meningioma link
- Design Defect: Pfizer's own lower-dose Depo-SubQ provides same efficacy with potentially less risk
- Corporate Admissions: Pfizer acknowledged the connection to The Guardian in March 2024
- FDA Database: 46 reported meningioma cases linked to the drug since 2000
This creates compelling evidence of a conscious decision to withhold critical safety information from American women while warning women in other countries.
Free case review • No obligation • Completely confidential