Zyrteccetirizine

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

118,971 adverse event reports submitted to the FDA (1995–2026)

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 Zyrtec 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
Zyrtec adverse event reports by reporter sex
SexReports
Female76,661
Male26,979
Unknown121

By Age Group

View age group data as a table
Zyrtec adverse event reports by reporter age group
Age groupReports
0-176,657
18-348,947
35-4916,874
50-6417,890
65-7410,660
75+7,132

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 Zyrtec. 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
Zyrtec adverse event reports by reported outcome
OutcomeReports
Non-Serious60,625
Other Serious44,005
Hospitalization24,088
Disability7,705
Death6,980
Life-Threatening6,350

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 Zyrtec. 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
Zyrtec adverse event reports by year
YearReports
19951
19981
19991
20021
20033
20041,241
20051,288
20061,241
20071,194
20081,333
20091,392
20101,867
20111,928
20122,521
20132,494
20143,138
20157,745
20168,376
20177,200
20187,292
20197,742
20208,547
20219,890
202210,408
20239,437
202410,299
202510,206
2026 (partial)2,185

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 Zyrtec

In FDA adverse event reports that mention Zyrtec, 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