Rolaids Power Chews 1000calcium carbonate

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

48,705 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 Rolaids Power Chews 1000 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
Rolaids Power Chews 1000 adverse event reports by reporter sex
SexReports
Female30,245
Male14,683
Unknown48

By Age Group

View age group data as a table
Rolaids Power Chews 1000 adverse event reports by reporter age group
Age groupReports
0-171,265
18-341,780
35-495,080
50-649,025
65-748,081
75+7,658

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 Rolaids Power Chews 1000. 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
Rolaids Power Chews 1000 adverse event reports by reported outcome
OutcomeReports
Other Serious27,982
Hospitalization22,649
Non-Serious7,593
Death7,179
Life-Threatening5,367
Disability4,189

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 Rolaids Power Chews 1000. 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
Rolaids Power Chews 1000 adverse event reports by year
YearReports
20021
20032
2004501
2005521
2006444
2007485
2008480
2009575
20101,310
20113,250
20123,376
20131,070
20141,116
20151,801
20162,163
20172,239
20182,983
20193,897
20203,478
20213,562
20223,699
20233,369
20243,945
20253,756
2026 (partial)682

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 Rolaids Power Chews 1000

In FDA adverse event reports that mention Rolaids Power Chews 1000, 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