Depo-Provera is a long-acting birth control injection containing medroxyprogesterone acetate, typically administered every three months to prevent pregnancy. While the medication has been widely used for decades, growing concerns have emerged about its potential long-term side effects. Many women have reported experiencing serious health issues following prolonged use of Depo-Provera, leading to an increase in product liability lawsuits against the manufacturer. These claims argue that the risks were not properly disclosed, leaving patients unaware of the potential dangers before beginning treatment.

Why Patients Are Filing Lawsuits

The primary allegations in Depo-Provera lawsuits focus on severe complications that may arise after repeated injections. Plaintiffs claim that the drug can cause significant bone density loss, sometimes leading to osteoporosis, fractures, or irreversible skeletal damage. Others report experiencing neurological issues, cardiovascular complications, and autoimmune-like symptoms after long-term use. Many lawsuits allege that the manufacturer failed to provide adequate warnings about the severity or permanence of these risks, especially for younger women whose bones are still developing.

Common Injuries and Long-Term Side Effects

Women filing Depo-Provera claims have reported a range of injuries including severe bone thinning, broken bones, joint pain, chronic fatigue, and hormonal imbalance. Some patients have experienced menstrual irregularities, fertility issues, depression, migraines, and mood disorders linked to hormone disruption. There are also claims involving vision problems, blood clots, and other systemic effects. In many cases, these complications required extensive medical treatment, long-term medications, lifestyle changes, or ongoing monitoring—significantly impacting quality of life.

Allegations Against the Manufacturer

Lawsuits allege that the manufacturer did not adequately warn patients or healthcare providers about the full extent of Depo-Provera’s potential side effects. While some risks were acknowledged, plaintiffs argue that crucial information regarding bone mineral density loss, fertility concerns, and long-term health effects was downplayed or not prominently disclosed. Many claims assert that women were not properly informed of safer alternatives or told about the importance of monitoring bone health while using the injection. As a result, thousands of women may have continued using the drug without understanding the potential for lasting or irreversible harm.

Who May Qualify for a Lawsuit

Individuals who have taken Depo-Provera and later suffered serious complications—particularly bone loss, fractures, osteoporosis, fertility issues, or severe hormonal or neurological symptoms—may qualify to file a claim. Younger patients, long-term users, and women who were not advised about bone-density monitoring may have especially strong cases. Families of women who experienced life-threatening complications, disability, or wrongful death may also be eligible to pursue legal action.