Good Sense Esomeprazole Magnesiumesomeprazole

According to the FDA label: Uses • treats frequent heartburn (occurs 2 or more days a week) • not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

46,294 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 →
New to FDA adverse event data? Here's how to read these reports →

Top Reported Adverse Events

The most frequently reported events in association with Good Sense 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
Good Sense Esomeprazole Magnesium adverse event reports by reporter sex
SexReports
Female22,932
Male17,319
Unknown60

By Age Group

View age group data as a table
Good Sense Esomeprazole Magnesium adverse event reports by reporter age group
Age groupReports
0-171,077
18-341,908
35-494,287
50-6410,545
65-748,621
75+8,271

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 Good Sense 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
Good Sense Esomeprazole Magnesium adverse event reports by reported outcome
OutcomeReports
Other Serious27,563
Hospitalization21,910
Death4,838
Non-Serious3,639
Life-Threatening3,509
Disability1,503

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 Good Sense 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
Good Sense Esomeprazole Magnesium adverse event reports by year
YearReports
20031
2004369
2005430
2006146
200787
2008188
2009282
2010461
2011356
2012523
2013871
20141,014
20151,400
20161,829
20172,140
20184,505
20196,035
20204,293
20213,677
20224,000
20234,234
20244,438
20254,148
2026 (partial)867

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 Good Sense Esomeprazole Magnesium

In FDA adverse event reports that mention Good Sense 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