Benadryldiphenhydramine

According to the FDA label: Uses: Temporarily relieves these symptoms due to the common cold, hay fever, or other upper respiratory allergies: runny nose sneezing itching of the nose or throat itchy, watery eyes

91,712 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 →
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 Benadryl 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
Benadryl adverse event reports by reporter sex
SexReports
Female54,239
Male24,316
Unknown108

By Age Group

View age group data as a table
Benadryl adverse event reports by reporter age group
Age groupReports
0-173,809
18-347,119
35-4911,761
50-6417,622
65-749,898
75+5,509

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 Benadryl. 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
Benadryl adverse event reports by reported outcome
OutcomeReports
Other Serious45,026
Non-Serious28,573
Hospitalization25,376
Death8,170
Life-Threatening3,588
Disability2,400

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 Benadryl. 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
Benadryl adverse event reports by year
YearReports
20031
20041,181
20051,356
20061,292
20071,011
20081,244
20091,478
20102,053
20112,065
20123,457
20132,472
20143,021
20154,865
20164,520
20174,521
20185,493
20196,318
20208,933
20217,877
20228,262
20237,007
20246,139
20255,787
2026 (partial)1,359

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 Benadryl

In FDA adverse event reports that mention Benadryl, 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