Depo-Provera Meningioma Lawsuit in Indiana
Last Updated: April 1, 2026
Indiana's position as a crossroads state with nearly 7 million residents and a significant pharmaceutical manufacturing presence — including Eli Lilly's headquarters in Indianapolis — gives its courts familiarity with drug liability issues. The state applies a two-year statute of limitations with a discovery rule for Depo-Provera and GLP-1 claims. Indiana's Product Liability Act provides a specific statutory framework that governs how pharmaceutical injury cases are litigated.
Depo-Provera (medroxyprogesterone acetate) has been linked to meningioma brain tumors. The FDA added a black-box warning in December 2025, and over 3,000 lawsuits have been filed nationwide. Indiana residents who used Depo-Provera and were diagnosed with a meningioma may qualify for compensation. The statute of limitations in Indiana for personal injury claims is 2 years. Attorneys handle these cases on a contingency fee basis — no cost unless you win.
Depo-Provera Meningioma Claims in Indiana
Depo-Provera (medroxyprogesterone acetate) has been linked to meningioma brain tumors. The FDA added a black-box warning in December 2025, and over 3,000 lawsuits have been filed nationwide. Indiana residents who used Depo-Provera and were diagnosed with a meningioma may qualify for compensation on a contingency fee basis — no cost unless you win.
In December 2025, the FDA took the significant step of updating Depo-Provera's label to include a formal warning about the elevated risk of meningioma associated with prolonged use. This label change came after years of accumulating scientific evidence — including studies from France and other countries — demonstrating a clear dose-response relationship between medroxyprogesterone acetate and meningioma development.
For Indiana residents who used Depo-Provera and were subsequently diagnosed with a meningioma, the legal landscape is now clear: the manufacturer knew or should have known about this risk and failed to provide adequate warnings. Over 3,000 lawsuits have been filed across the country, and Indiana residents are actively filing claims to seek compensation for their injuries.
Meningiomas, while often classified as benign tumors, can cause devastating symptoms including chronic headaches, seizures, vision and hearing problems, cognitive impairment, and personality changes. Treatment frequently requires invasive brain surgery, radiation therapy, or both. Many patients face recurring tumors and lifelong monitoring.
Indiana legal landscape: Indiana's Product Liability Act (Ind. Code 34-20) is the exclusive remedy for product defect claims and applies a fault-based standard rather than pure strict liability. The state follows modified comparative fault with a 50% bar and recognizes the learned intermediary doctrine. Residents in Indianapolis, Fort Wayne, Evansville, and South Bend and surrounding areas should consult with an attorney experienced in pharmaceutical litigation to evaluate their potential claim.
Indiana Statute of Limitations
Understanding the statute of limitations is critical for Indiana residents considering a Depo-Provera meningioma lawsuit. In Indiana, the statute of limitations for personal injury claims is 2 years. For product liability claims specifically, the deadline is 2 years.
Indiana recognizes the discovery rule, which is particularly important in pharmaceutical injury cases. Under this rule, the statute of limitations may begin running not from the date of your last Depo-Provera injection, but from the date you discovered — or reasonably should have discovered — the connection between Depo-Provera and your meningioma. Given that the FDA only formally warned about this risk in December 2025, many Indiana residents may still be within their filing window even if their diagnosis occurred years ago.
Do not assume your deadline has passed without consulting an attorney. The interplay between personal injury and product liability statutes, the discovery rule, and the facts of your specific case can create nuances that only a qualified legal professional can properly evaluate.
Personal Injury SOL
2 years
Product Liability SOL
2 years
Discovery Rule
Yes
How to File a Depo-Provera Lawsuit in Indiana
Filing a Depo-Provera meningioma lawsuit in Indiana involves several steps, but the process begins with a simple, no-cost case evaluation. Here is what to expect:
Free Case Review
Complete a free case evaluation to determine whether your Depo-Provera usage and meningioma diagnosis qualify for legal action under Indiana law.
Attorney Referral
If your case qualifies, you will be connected with experienced mass tort attorneys licensed to practice in Indiana who specialize in pharmaceutical litigation.
Case Filing
Your attorney will file your claim in the appropriate court. In Indiana, cases may be filed in the Indiana Circuit Courts or in federal court (Northern District of Indiana and other federal districts).
Litigation & Resolution
Your legal team handles all proceedings including discovery, depositions, and trial preparation. You pay nothing unless you receive compensation through settlement or verdict.
Do You Qualify in Indiana?
Indiana residents may be eligible to file a Depo-Provera meningioma claim if the following criteria are met:
Used Depo-Provera Injections
You received one or more Depo-Provera (medroxyprogesterone acetate) injections while residing in Indiana or another state.
Diagnosed with a Meningioma
You have been diagnosed with a meningioma brain tumor, confirmed through imaging (MRI or CT scan) or surgical pathology.
Timeline Consistent with Causation
Your meningioma diagnosis occurred after you began receiving Depo-Provera injections, establishing a timeline that supports a causal connection.
Within the Filing Deadline
Your claim falls within Indiana's statute of limitations (2 years for personal injury). The discovery rule may extend this deadline — an attorney can evaluate your specific timeline.
Indiana Depo-Provera FAQ
What is a meningioma and how is it linked to Depo-Provera in Indiana?
A meningioma is a tumor that forms on the membranes covering the brain and spinal cord. In December 2025, the FDA updated Depo-Provera's label to warn about the increased risk of meningioma brain tumors. Indiana residents who used Depo-Provera and were later diagnosed with a meningioma may be eligible to file a claim. Multiple studies have shown that prolonged use of medroxyprogesterone acetate, the active ingredient in Depo-Provera, is associated with a significantly elevated risk of developing meningiomas.
What is the statute of limitations for a Depo-Provera lawsuit in Indiana?
In Indiana, the statute of limitations for personal injury claims is 2 years from the date of injury or discovery. Indiana recognizes the discovery rule, which means the clock may start when you discovered — or reasonably should have discovered — the connection between Depo-Provera and your meningioma, rather than the date of your last injection. Because these deadlines are strict and missing them can permanently bar your claim, prompt action is critical.
How do I file a Depo-Provera meningioma lawsuit in Indiana?
Filing a Depo-Provera meningioma lawsuit in Indiana begins with a free case review to determine your eligibility. If your case qualifies, you will be connected with experienced mass tort attorneys who can file your claim in either the Indiana Circuit Courts or the appropriate federal district court. Most cases are being consolidated in federal multidistrict litigation (MDL) for efficiency. Your attorney handles all legal filings and proceedings on your behalf.
What compensation is available for Indiana Depo-Provera victims?
Indiana residents who qualify may be entitled to compensation for medical expenses (surgery, radiation, imaging, hospital stays, and ongoing monitoring), lost wages and diminished earning capacity, pain and suffering, and emotional distress. The amount of compensation depends on the severity of your meningioma, the treatment required, and the impact on your daily life and ability to work.
Which courts handle Depo-Provera cases in Indiana?
Depo-Provera meningioma cases in Indiana can be filed in the Indiana Circuit Courts at the state level or in federal court. The federal districts covering Indiana include the Northern District of Indiana, Southern District of Indiana. Many cases are being consolidated in a federal multidistrict litigation (MDL) for pretrial proceedings, with individual cases returning to their home districts for trial if needed.
Does it cost anything to file a Depo-Provera claim in Indiana?
There is no upfront cost to file a Depo-Provera meningioma claim in Indiana. Attorneys handling these cases work on a contingency fee basis, meaning they only receive payment if you obtain compensation through a settlement or trial verdict. NuLegal's initial case review is completely free with no obligation to proceed.
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Indiana Residents: Don't Wait
The statute of limitations in Indiana is 2 years for personal injury claims. Get a free, no-obligation case review today to find out if you qualify for compensation.
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Disclosure: NuLegal operates as a legal referral service. Attorney Ashkaan Hassan evaluates claims and refers qualified cases to specialized trial firms, earning a referral fee from the attorney's share of any recovery. Clients never pay out of pocket.