Ambien CRzolpidem

84,701 adverse event reports submitted to the FDA (2001–2026)

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 Ambien CR 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
Ambien CR adverse event reports by reporter sex
SexReports
Female52,499
Male27,460
Unknown203

By Age Group

View age group data as a table
Ambien CR adverse event reports by reporter age group
Age groupReports
0-17517
18-344,447
35-4911,044
50-6418,623
65-7410,404
75+7,592

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 Ambien CR. 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
Ambien CR adverse event reports by reported outcome
OutcomeReports
Other Serious32,962
Non-Serious31,076
Hospitalization26,277
Death7,383
Life-Threatening3,044
Disability2,423

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 Ambien CR. 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
Ambien CR adverse event reports by year
YearReports
20011
20021
20033
20041,920
20052,501
20063,323
20073,219
20082,648
20093,416
20103,964
20113,705
20124,791
20133,999
20143,971
20156,133
20166,650
20174,954
20186,106
20194,672
20203,851
20212,891
20222,985
20232,724
20242,800
20252,841
2026 (partial)632

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 Ambien CR

In FDA adverse event reports that mention Ambien CR, 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