What Is Depo-Provera?
Depo-Provera is the brand name for medroxyprogesterone acetate, a hormonal contraceptive that contains the hormone progestin. The medication is delivered as an injectable birth control shot that must be administered once every three months. Depo-Provera prevents pregnancy through several mechanisms:- Stopping ovulation by preventing the ovaries from releasing an egg;
- Thickening cervical mucus, which blocks sperm from reaching the egg; and
- Thinning the uterine lining, making implantation less likely.
Known Depo-Provera Side Effects
Like many hormonal medications, Depo-Provera can cause a variety of side effects. Some are mild and temporary, while others may become more serious with long-term use. Commonly reported side effects include:- Irregular periods and breakthrough bleeding
- Weight gain
- Bloating or abdominal discomfort
- Reduced interest in sex
- Nervousness or mood changes;
Emerging Concerns: Brain Tumors and Meningioma Risk
More recently, research has identified a possible link between long-term use of certain medroxyprogesterone and intracranial meningiomas. Meningiomas are tumors that develop in the membranes surrounding the brain and spinal cord. While they are usually noncancerous, they can still cause serious health complications as they grow and press against surrounding brain tissue, nerves, or blood vessels. Symptoms associated with meningiomas may include:- Persistent headaches
- Vision changes or vision loss
- Seizures
- Balance and coordination problems
- Memory issues or personality changes
- Speech difficulties
- Weakness or numbness on one side of the body.
Key Findings from the 2024 BMJ Study
A major study published in The BMJ in March 2024 analyzed data from the French National Health Data System to better understand the relationship between hormonal medications and meningioma risk. The population-based case-control study reviewed data from 108,366 women, including 18,061 women in France who underwent intracranial surgery for meningioma between 2009 and 2018. Researchers found that prolonged use of medroxyprogesterone acetate injections was associated with a significantly increased risk of developing meningiomas requiring surgery. Key findings included:- Women who used Depo-Provera long-term had a 5.6-fold increased risk of developing meningioma;
- The increased risk was primarily linked to use lasting one year or longer; and
- The study identified an association between meningioma risk and several progestogens, including medroxyprogesterone acetate injection (150 mg).
Recently Updated FDA Warning on Depo-Provera
In response to growing safety concerns, and as pressure mounts through early litigation in multiple courts around the United States, regulators have begun updating prescribing information for the medication. In December 2025, the U.S. Food and Drug Administration (FDA), in response to mounting pressure created through litigation against the manufacturers of Depo-Provera, approved an updated label for Depo-Provera that includes a warning about the potential risk of meningioma. The updated guidance encourages healthcare providers to monitor patients using Depo-Provera for possible signs of meningioma, particularly among individuals who have used the medication for extended periods. This updated label warning represents the first time the manufacturers of Depo-Provera have informed patients of the increased risk of developing meningioma tumors after prolonged Depo-Provera use.Additional Reported Health Concerns
In addition to bone loss and tumor risks, Depo-Provera has also been associated with other neurological and systemic side effects. Some research has also examined a possible connection between Depo-Provera use and breast cancer, with one study finding increased risk among women who used the injection for 12 months or longer. Adverse event reporting systems have also documented thousands of neoplasm-related reports, including both benign and malignant tumors, associated with the drug over several decades.Legal Options for Women Affected by Depo-Provera
As new scientific evidence emerges, lawsuits are being filed on behalf of women who developed meningiomas or other serious complications after using Depo-Provera. Women who may qualify for legal action include those who:- Used Depo-Provera for one year or longer;
- Were later diagnosed with meningioma; and
- Required brain surgery or medical treatment related to the condition.
- Medical expenses
- Lost income
- Pain and suffering
- Long-term care needs
