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Campaigns people are reviewing now

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Featured campaignAccepting reviews

Depo-Provera (meningioma)

People who used the Depo-Provera birth-control shot and were later diagnosed with a meningioma may want their situation reviewed. The FDA added meningioma to the drug's warnings in late 2025.

Federal case group
MDL 3140
pending cases, Sep 1, 2026
6,403
source for case count
JPML

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  1. Find what happened to youBrowse by situation or search a product. Each page lists the criteria participating firms review.
  2. Read the facts and sourcesCurrent status, the court or agency behind it, and the records that usually help.
  3. Answer a few questionsAbout three minutes. “I'm not sure” is always an option.
  4. A participating firm follows upOnly with your consent. The firm alone decides whether to take a case.

What changed, and where it came from

All updates
  1. JPML
    Monthly pending-case report publishedPending-case counts refreshed on every campaign page with a federal case group, after editor review.
    View source (opens in a new tab)
  2. Pfizer
    Oxbryta will not return to the U.S. marketStatus stays at Monitoring. There is no consolidated federal case group at this time.
    View source (opens in a new tab)
  3. FDA
    Meningioma added to Depo-Provera warningsFDA approved labeling that adds meningioma to Warnings and Precautions.
    View source (opens in a new tab)
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