Tylenol Cold Plus Head Congestion Severeacetaminophen + guaifenesin + phenylephrine

156,043 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 Tylenol Cold Plus Head Congestion Severe 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
Tylenol Cold Plus Head Congestion Severe adverse event reports by reporter sex
SexReports
Female93,505
Male42,738
Unknown140

By Age Group

View age group data as a table
Tylenol Cold Plus Head Congestion Severe adverse event reports by reporter age group
Age groupReports
0-174,017
18-347,507
35-4914,326
50-6426,090
65-7420,044
75+19,082

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 Tylenol Cold Plus Head Congestion Severe. 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
Tylenol Cold Plus Head Congestion Severe adverse event reports by reported outcome
OutcomeReports
Other Serious63,953
Non-Serious63,351
Hospitalization40,651
Death11,867
Disability5,098
Life-Threatening4,755

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 Tylenol Cold Plus Head Congestion Severe. 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
Tylenol Cold Plus Head Congestion Severe adverse event reports by year
YearReports
19991
20011
20032
20041,267
20051,081
2006839
20071,047
2008749
2009982
20101,320
2011514
20123,092
20133,851
20144,771
20158,678
20169,190
20179,931
201811,509
201913,632
202014,200
202115,181
202212,717
202311,784
202411,827
202515,138
2026 (partial)2,739

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 Tylenol Cold Plus Head Congestion Severe

In FDA adverse event reports that mention Tylenol Cold Plus Head Congestion Severe, 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