
Depo-Provera is a widely used contraceptive marketed under the brand names Depo-Provera and the lower-dose Depo-SubQ Provera 104.
Depo-Provera is a hormonal birth control injection approved by the U.S. Food and Drug Administration (FDA) in 1992 and inhibits ovulation by thickening cervical mucus and thinning the uterine lining. It is typically into the arm or the buttocks every 12 weeks.
Depo-Provera is highly effective and may also be prescribed for managing other conditions, such as:
Cancer Treatement
Hirsutism
Chronic Pelvic Pain
Menstrual Disorders
Contraception
Uterine Fibroids
Cancer Treatement
Hirsutism
Chronic Pelvic Pain
Menstrual Disorders
Contraception
Uterine Fibroids
Endometriosis
Reduced Cancer Risk
Hormonal Imbalances
Reduced Ovarian Cysts
Post-Partum Bleeding
In recent years, Depo-Provera has come under scrutiny after research linked the drug’s ingredients to an increased risk of meningioma brain tumors.
Endometriosis
Reduced Cancer Risk
Hormonal Imbalances
Reduced Ovarian Cysts
Post-Partum Bleeding

In recent years, Depo-Provera has come under scrutiny after research linked the drug’s ingredients to an increased risk of meningioma brain tumors.
Medical research indicates that long-term use of medroxyprogesterone acetate (MPA), the active ingredient in Depo-Provera, causes more than five times the risk for brain tumors. MPA binds to progesterone receptors in the protective layers surrounding the brain and spinal cord, triggering abnormal cell growth that may contribute to the development of meningiomas.
With such increased risks and approximately 74 million users globally, Depo-Provera may be considered a potentially significant public health concern.


Symptoms of meningioma vary depending on the size and location of the tumor and include:
Cancer Treatement
Loss of Balance Or Vertigo
Chronic Pelvic Pain
Menstrual Disorders
Contraception
Seizures
Difficulty Speaking
Hearing Loss
Loss Of Smell
Memory Loss
Weakness In Limbs


Depo-Provera is linked to an increased risk of meningioma and other brain tumors. Early indications reveal that Pfizer knew or should have known about the risks but failed to warn healthcare professionals or consumers.
Women who have received at least two Depo-Provera injections may qualify for compensation if they have been diagnosed with any of the following conditions:
Benign or malignant brain tumors
Meningioma
Pseudotumor cerebri
We are investigating claims for women who have been administered Depo-Provera injections and subsequently been diagnosed with brain tumors that could have been avoided with adequate warnings about the risk. As more information about the risks associated with Depo-Provera becomes available, we anticipate an increase in lawsuits against Pfizer in the coming years.
We are committed to assisting women who have brain tumors after receiving Depo-Prover. If you have been diagnosed with meningioma or other brain tumors, complete our online form or call us today to learn how we can help.
To be eligible for a Depo-Provera lawsuit, you must meet the following criteria:
Must have been administered at least two injections of brand-name Depo-Provera, depo-SubQ Provera, or an authorized generic version.
Must be diagnosed with meningioma or other brain tumors after using Depo-Provera.
The length of time Depo-Provera or its generic version was used, the time since the last dose, and the timing of the diagnosis of meningioma or other brain tumors.
Your information will be kept confidential.
Disclaimer: Depo-Provera litigation is just beginning, and no settlements or verdicts have been awarded thus far.