Tums Regular Strengthcalcium carbonate

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

61,631 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 Regular Strength 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.

Show these terms with plain-language definitions

Tap any term below for a plain-language definition.

Browse the full glossary →

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 Regular Strength adverse event reports by reporter sex
SexReports
Female38,200
Male18,600
Unknown62

By Age Group

View age group data as a table
Tums Regular Strength adverse event reports by reporter age group
Age groupReports
0-171,512
18-342,296
35-496,400
50-6411,401
65-749,833
75+9,177

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 Regular Strength. 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 Regular Strength adverse event reports by reported outcome
OutcomeReports
Other Serious34,446
Hospitalization26,537
Non-Serious11,840
Death8,541
Life-Threatening6,086
Disability5,038

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 Regular Strength. 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 Regular Strength adverse event reports by year
YearReports
20021
20032
2004592
2005640
2006555
2007623
2008623
2009803
20101,468
20113,357
20123,639
20131,475
20141,566
20152,552
20162,834
20173,004
20184,254
20195,519
20204,606
20214,550
20224,398
20233,980
20244,882
20254,821
2026 (partial)887

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 Regular Strength

In FDA adverse event reports that mention Tums Regular Strength, 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