Tums Ultracalcium carbonate

According to the FDA label: Uses relieves • heartburn • acid indigestion • sour stomach • upset stomach associated with these symptoms

62,353 adverse event reports submitted to the FDA (2002–2026)

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 Tums Ultra 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
Tums Ultra adverse event reports by reporter sex
SexReports
Female38,685
Male18,756
Unknown62

By Age Group

View age group data as a table
Tums Ultra adverse event reports by reporter age group
Age groupReports
0-171,522
18-342,312
35-496,578
50-6411,483
65-749,929
75+9,260

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 Tums Ultra. 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
Tums Ultra adverse event reports by reported outcome
OutcomeReports
Other Serious34,874
Hospitalization26,851
Non-Serious12,054
Death8,760
Life-Threatening6,299
Disability5,234

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 Tums Ultra. 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
Tums Ultra adverse event reports by year
YearReports
20021
20032
2004592
2005642
2006554
2007625
2008623
2009805
20101,469
20113,358
20123,643
20131,485
20141,571
20152,568
20162,869
20173,048
20184,287
20195,546
20204,635
20214,593
20224,432
20234,019
20245,086
20254,997
2026 (partial)903

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 Tums Ultra

In FDA adverse event reports that mention Tums Ultra, 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