Ferrum Metallicumiron

According to the FDA label: INDICATIONS Condition listed above or as directed by the physician

65,131 adverse event reports submitted to the FDA (2002–2026)

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 Ferrum Metallicum 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
Ferrum Metallicum adverse event reports by reporter sex
SexReports
Female42,211
Male17,979
Unknown75

By Age Group

View age group data as a table
Ferrum Metallicum adverse event reports by reporter age group
Age groupReports
0-172,040
18-345,570
35-497,034
50-6410,164
65-748,570
75+8,509

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 Ferrum Metallicum. 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
Ferrum Metallicum adverse event reports by reported outcome
OutcomeReports
Other Serious28,780
Non-Serious22,769
Hospitalization20,312
Death4,639
Life-Threatening1,569
Disability1,546

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 Ferrum Metallicum. 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
Ferrum Metallicum adverse event reports by year
YearReports
20021
20031
2004454
2005441
2006450
2007523
2008685
2009975
20101,337
20111,088
20122,129
20132,312
20142,950
20154,386
20164,761
20174,196
20184,557
20194,806
20205,174
20214,775
20224,683
20234,400
20244,384
20254,579
2026 (partial)1,084

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 Ferrum Metallicum

In FDA adverse event reports that mention Ferrum Metallicum, 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