Adrenalinum

40,057 adverse event reports submitted to the FDA (1999–2026)

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 Adrenalinum 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
Adrenalinum adverse event reports by reporter sex
SexReports
Female21,716
Male12,373
Unknown54

By Age Group

View age group data as a table
Adrenalinum adverse event reports by reporter age group
Age groupReports
0-173,364
18-343,328
35-493,999
50-645,689
65-743,542
75+2,009

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 Adrenalinum. 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
Adrenalinum adverse event reports by reported outcome
OutcomeReports
Other Serious17,347
Non-Serious14,918
Hospitalization13,307
Life-Threatening4,036
Death3,448
Disability377

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 Adrenalinum. 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
Adrenalinum adverse event reports by year
YearReports
19992
20021
2004133
2005118
2006136
2007166
2008194
2009269
2010261
2011703
2012425
2013301
2014409
2015635
20161,057
20171,570
20182,474
20193,337
20206,460
20213,908
20223,583
20233,779
20244,420
20254,672
2026 (partial)1,044

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 Adrenalinum

In FDA adverse event reports that mention Adrenalinum, 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