Quetiapine Fumarate

According to the FDA label: Quetiapine Extended-release tablet is an atypical antipsychotic indicated for the treatment of: Schizophrenia (1.1) Bipolar I disorder, manic, or mixed episodes (1.2) Bipolar disorder, depressive episodes (1.2) Major depressive disorder, adjunctive therapy with antidepressants (1.3) 1.1 Schizophrenia Quetiapine Extended-release tablets are indicated for the treatment of schizophrenia.

103,771 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 Quetiapine Fumarate 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
Quetiapine Fumarate adverse event reports by reporter sex
SexReports
Female55,076
Male38,911
Unknown265

By Age Group

View age group data as a table
Quetiapine Fumarate adverse event reports by reporter age group
Age groupReports
0-174,825
18-3416,328
35-4920,344
50-6419,498
65-749,466
75+10,308

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 Quetiapine Fumarate. 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
Quetiapine Fumarate adverse event reports by reported outcome
OutcomeReports
Other Serious59,617
Hospitalization45,442
Death21,332
Life-Threatening11,552
Non-Serious8,763
Disability5,516

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 Quetiapine Fumarate. 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
Quetiapine Fumarate adverse event reports by year
YearReports
20011
20031
2004265
2005592
2006548
2007514
2008802
2009818
2010979
20111,215
20121,824
20131,967
20142,746
20153,547
20163,818
20176,005
20188,017
20199,166
20209,498
20219,649
20229,546
20239,505
202410,243
20259,996
2026 (partial)2,509

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 Quetiapine Fumarate

In FDA adverse event reports that mention Quetiapine Fumarate, 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