Baclofen (intrathecal)

84,437 adverse event reports submitted to the FDA (2003–2026)

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 Baclofen (intrathecal) 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
Baclofen (intrathecal) adverse event reports by reporter sex
SexReports
Female52,182
Male26,379
Unknown172

By Age Group

View age group data as a table
Baclofen (intrathecal) adverse event reports by reporter age group
Age groupReports
0-172,396
18-345,005
35-4913,615
50-6421,485
65-748,484
75+3,197

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 Baclofen (intrathecal). 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
Baclofen (intrathecal) adverse event reports by reported outcome
OutcomeReports
Other Serious35,329
Non-Serious28,247
Hospitalization27,622
Death6,354
Life-Threatening2,720
Disability2,134

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 Baclofen (intrathecal). 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
Baclofen (intrathecal) adverse event reports by year
YearReports
20033
2004646
2005757
2006674
2007796
2008886
20091,032
20101,499
20111,742
20122,549
20133,349
20144,724
20155,493
20167,662
20177,028
20187,708
20196,673
20205,776
20215,486
20225,095
20235,669
20244,218
20254,029
2026 (partial)943

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 Baclofen (intrathecal)

In FDA adverse event reports that mention Baclofen (intrathecal), 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