Esomeprazole Magnesium

59,790 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 Esomeprazole Magnesium 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
Esomeprazole Magnesium adverse event reports by reporter sex
SexReports
Female30,306
Male22,103
Unknown75

By Age Group

View age group data as a table
Esomeprazole Magnesium adverse event reports by reporter age group
Age groupReports
0-171,270
18-342,312
35-495,405
50-6413,275
65-7410,744
75+9,998

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 Esomeprazole Magnesium. 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
Esomeprazole Magnesium adverse event reports by reported outcome
OutcomeReports
Other Serious34,314
Hospitalization27,008
Non-Serious6,952
Death6,009
Life-Threatening4,243
Disability1,968

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 Esomeprazole Magnesium. 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
Esomeprazole Magnesium adverse event reports by year
YearReports
20031
2004416
2005502
2006349
2007528
2008958
2009767
2010849
2011727
2012798
2013992
20141,149
20151,660
20162,297
20172,675
20185,565
20197,258
20205,073
20214,574
20225,193
20235,429
20245,619
20255,322
2026 (partial)1,089

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 Esomeprazole Magnesium

In FDA adverse event reports that mention Esomeprazole Magnesium, 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