Pantoprazole

190,015 adverse event reports submitted to the FDA (2003–2026)

This data reflects voluntary reports submitted to the FDA's Adverse Event Monitoring System (AEMS), formerly the FDA Adverse Event Reporting System (FAERS). A report does not mean the medication caused the event. Data may be incomplete or contain errors. Learn more about AEMS. New to this data? Read our guide on how to interpret FDA adverse event reports →
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Top Reported Adverse Events

The most frequently reported events in association with Pantoprazole in the FAERS database. These are events reported by patients taking this medication, not necessarily caused by it. A single report may include multiple events.

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Ranked by frequency of reports, not severity. The most-reported event is not necessarily the most dangerous or the most common in patients taking this drug.

Who Is Reporting

Demographics of patients in FAERS reports that included this information. Not all reports include patient demographics.

By Sex

View reporter sex data as a table
Pantoprazole adverse event reports by reporter sex
SexReports
Female97,782
Male73,843
Unknown163

By Age Group

View age group data as a table
Pantoprazole adverse event reports by reporter age group
Age groupReports
0-172,139
18-346,323
35-4917,393
50-6439,178
65-7436,852
75+36,267

This shows who filed reports, reflecting who takes this drug and who tends to report, not who is at greatest risk.

Reported Outcomes

Outcomes recorded in FAERS reports that included Pantoprazole. A single report may involve multiple reactions, each with a different outcome. These categories are defined by FDA reporting guidelines, not by PillSignal.

View outcome data as a table
Pantoprazole adverse event reports by reported outcome
OutcomeReports
Other Serious102,162
Hospitalization88,528
Non-Serious28,968
Death21,370
Life-Threatening13,593
Disability7,191

Serious outcomes are far more likely to be reported than mild ones, so this overstates how often outcomes are serious. A recorded death does not mean the drug caused it.

Number of FAERS reports received per quarter for Pantoprazole. Changes in volume may reflect shifts in prescribing rates, media attention, or reporting behavior, not changes in the medication's safety profile.

View report trend as a table
Pantoprazole adverse event reports by year
YearReports
20033
2004462
2005462
2006256
2007104
2008255
2009433
20101,661
20112,785
20123,963
20133,483
20145,153
20157,731
20169,600
201710,733
201817,411
201921,854
202019,735
202118,927
202217,493
202315,102
202415,205
202514,098
2026 (partial)3,106

The steep increase around 2004 reflects the FDA's move to electronic submission, not a change in this drug's safety. Trends track reporting volume, not risk.

Medications commonly reported with Pantoprazole

In FDA adverse event reports that mention Pantoprazole, these medications appeared most often in the same report.

This reflects co-occurrence in submitted reports, not evidence of drug interaction or combined risk. People often report several medications taken for the same condition or for unrelated reasons. Talk to a doctor or pharmacist about your specific medications.

Other medications with similar adverse event profiles in FDA FAERS reports.

Data Source

This data is sourced from the FDA's Adverse Event Monitoring System (AEMS), formerly FAERS, via the OpenFDA API. PillSignal is not affiliated with the FDA.

View this data on the FDA website →

Data last updated: June 2026