Minoxidil (for Men)

According to the FDA label: INDICATIONS & USAGE SECTION

32,266 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 →
New to FDA adverse event data? Here's how to read these reports →

Top Reported Adverse Events

The most frequently reported events in association with Minoxidil (for Men) 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
Minoxidil (for Men) adverse event reports by reporter sex
SexReports
Male23,587
Female7,089
Unknown13

By Age Group

View age group data as a table
Minoxidil (for Men) adverse event reports by reporter age group
Age groupReports
0-17307
18-34977
35-491,375
50-642,092
65-741,672
75+1,051

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 Minoxidil (for Men). 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
Minoxidil (for Men) adverse event reports by reported outcome
OutcomeReports
Non-Serious27,845
Other Serious2,889
Hospitalization2,005
Death445
Disability266
Life-Threatening240

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 Minoxidil (for Men). 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
Minoxidil (for Men) adverse event reports by year
YearReports
200495
2005122
2006127
200789
2008113
2009130
2010149
2011170
2012220
2013152
2014196
2015588
2016833
2017794
2018967
2019981
20202,458
20214,839
20227,986
20235,654
20243,109
20252,219
2026 (partial)275

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 Minoxidil (for Men)

In FDA adverse event reports that mention Minoxidil (for Men), 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