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Litigation Stage Tracker
Early / Monitoring

Proton Pump Inhibitors

ClosedFLAT
MDL 2789Pharma
12,000+
Total Cases

Causation

Long-term use of proton pump inhibitors is linked to chronic kidney disease, acute interstitial nephritis, and end-stage renal failure. A 2016 JAMA Internal Medicine study found 20-50% increased risk of chronic kidney disease with PPI use. The mechanism involves PPI-induced magnesium depletion, direct nephrotoxicity, and chronic interstitial inflammation. Plaintiffs allege manufacturers knew of kidney injury signals from post-marketing surveillance and failed to update labels.

Defendants

EntityRoleNote
AstraZenecaManufacturerNexium (esomeprazole) and Prilosec (omeprazole) — primary defendant
Pfizer Inc.ManufacturerProtonix (pantoprazole) — co-defendant
Procter & GambleMarketerMarketed OTC Prilosec under consumer health division
Takeda PharmaceuticalManufacturerPrevacid (lansoprazole) — co-defendant

Litigation Timeline

2016
JAMA Internal Medicine: 20-50% increased CKD risk with PPI use
2019
Bellwether case selection completed
2020
First bellwether trial scheduled — delayed by COVID-19
2022-2023
Settlement programs resolve majority of cases
2025-2026
12,000+ cases filed — most resolved. Monitoring residual claims

Intelligence Signals

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Key Facts

Status
active

Geographic Exposure

·D.N.J. (MDL 2789, Judge McNulty)
·Nationwide filing — all 50 states
·Most cases resolved through settlement programs

Eligibility Criteria

  • Used a PPI (Nexium, Prilosec, Prevacid, Protonix, or generic) for 1+ years
  • Diagnosed with chronic kidney disease, acute kidney injury, or renal failure
  • Kidney injury occurred during or after long-term PPI use
  • No pre-existing kidney disease before PPI use