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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

ACETAMINOPHEN\DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN: 64 Adverse Event Reports & Safety Profile

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64
Total FAERS Reports
0
Deaths Reported
1
Hospitalizations
64
As Primary/Secondary Suspect

First Report: 200604 · Latest Report: 20250408

What Are the Most Common ACETAMINOPHEN\DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN Side Effects?

#1 Most Reported
Choking
31 reports (48.4%)
#2 Most Reported
Foreign body in throat
27 reports (42.2%)
#3 Most Reported
Product use complaint
15 reports (23.4%)

All ACETAMINOPHEN\DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Choking 31 48.4% 0 0
Foreign body in throat 27 42.2% 0 0
Product use complaint 15 23.4% 0 0
Incorrect dose administered 10 15.6% 0 1
Dyspnoea 6 9.4% 0 0
Oropharyngeal pain 6 9.4% 0 0

Who Reports ACETAMINOPHEN\DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN Side Effects? Age & Gender Data

Gender: 72.0% female, 28.0% male. Average age: 74.1 years. Most reports from: US. View detailed demographics →

Is ACETAMINOPHEN\DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN Getting Safer? Reports by Year

YearReportsDeathsHosp.
2006 1 0 1
2020 6 0 0
2021 11 0 0
2022 9 0 0
2023 3 0 0
2024 2 0 0
2025 3 0 0

View full timeline →

What Is ACETAMINOPHEN\DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN Used For?

IndicationReports
Nasopharyngitis 34
Hypersensitivity 27
Product used for unknown indication 7

Official FDA Label for ACETAMINOPHEN\DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN

Official prescribing information from the FDA-approved drug label.