Depo-Provera Free Case Review
Lawsuits against Depo‑Provera allege that brand-name and generic versions of this birth control injection may be linked to an increased risk of meningiomas, typically benign brain tumors. Plaintiffs claim Pfizer and other manufacturers failed to adequately warn users. While no jury verdicts or mass settlements have been finalized, a federal MDL was established in February 2025 and currently includes over 550 consolidated claims as of July 2025, with additional cases moving forward in state courts
Depo‑Provera and Brain Tumors
A March 2024 study in the British Medical Journal reported that women using Depo‑Provera for 12 months or longer had a 5.6‑fold increased risk of meningioma.
The FDA has not required a U.S. label warning about brain‑tumor risk, despite similar warnings being added in the EU and UK
Do I Qualify for a Depo‑Provera Lawsuit?
You may be eligible if all of the following apply:
You received Depo‑Provera, Depo‑SubQ Provera, or an authorized generic.
You used it for at least a year (typically two or more injections).
You received a meningioma diagnosis after beginning the injections.
Your case meets state-specific filing deadlines (commonly 2–3 years post‑diagnosis).
Requirements vary by state and injury specifics. Contact a qualified Depo‑Provera attorney to assess your case.
What’s Happening Now
Feb 2025: MDL 3140 formed in the Northern District of Florida under Judge Casey Rodgers.
By Jul 2025: Over 550 Depo-related lawsuits are consolidated, with initial “bellwether” cases selected to help shape future settlements.
Evidence gathering: Ongoing document exchanges, with more than 8,000 documents produced.
Next steps: Discovery, case management orders, and early trials could begin in 2025–26.
Case Review
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