Methotrexate Sodium

75,169 adverse event reports submitted to the FDA (2004–2026)

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 Methotrexate Sodium 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
Methotrexate Sodium adverse event reports by reporter sex
SexReports
Female51,471
Male18,757
Unknown58

By Age Group

View age group data as a table
Methotrexate Sodium adverse event reports by reporter age group
Age groupReports
0-174,219
18-344,190
35-499,958
50-6421,279
65-7413,569
75+6,700

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 Methotrexate Sodium. 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
Methotrexate Sodium adverse event reports by reported outcome
OutcomeReports
Other Serious37,269
Non-Serious28,511
Hospitalization15,691
Death4,343
Life-Threatening3,669
Disability2,395

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 Methotrexate Sodium. 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
Methotrexate Sodium adverse event reports by year
YearReports
2004767
2005506
2006181
2007248
2008267
2009263
2010162
2011385
2012682
2013772
2014513
20151,132
20164,126
201710,225
201812,492
20199,175
20206,836
20214,865
20226,012
20235,997
20245,139
20253,828
2026 (partial)596

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 Methotrexate Sodium

In FDA adverse event reports that mention Methotrexate Sodium, 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