Albuterol

195,629 adverse event reports submitted to the FDA (1995–2026)

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 Albuterol 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
Albuterol adverse event reports by reporter sex
SexReports
Female108,841
Male60,133
Unknown180

By Age Group

View age group data as a table
Albuterol adverse event reports by reporter age group
Age groupReports
0-179,531
18-3410,802
35-4916,729
50-6432,990
65-7424,726
75+20,313

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 Albuterol. 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
Albuterol adverse event reports by reported outcome
OutcomeReports
Non-Serious84,976
Other Serious70,807
Hospitalization58,241
Death13,100
Life-Threatening6,997
Disability5,014

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 Albuterol. 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
Albuterol adverse event reports by year
YearReports
19951
19982
20032
20042,811
20052,955
20062,405
20072,843
20083,261
20093,327
20104,200
20113,791
20125,080
20133,942
20144,515
20156,467
20167,737
20176,216
20186,630
20197,343
202010,827
202114,738
202219,325
202321,991
202424,491
202525,282
2026 (partial)5,447

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 Albuterol

In FDA adverse event reports that mention Albuterol, 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