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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.

ALBUTEROL\GUAIFENESIN: 54 Adverse Event Reports & Safety Profile

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54
Total FAERS Reports
2 (3.7%)
Deaths Reported
23
Hospitalizations
54
As Primary/Secondary Suspect
1
Life-Threatening
7
Disabilities

First Report: 20090609 · Latest Report: 20240126

What Are the Most Common ALBUTEROL\GUAIFENESIN Side Effects?

#1 Most Reported
Asthma
28 reports (51.9%)
#2 Most Reported
Hypersensitivity
23 reports (42.6%)
#3 Most Reported
Food allergy
23 reports (42.6%)

All ALBUTEROL\GUAIFENESIN Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Asthma 28 51.9% 2 22
Food allergy 23 42.6% 2 0
Hypersensitivity 23 42.6% 1 0
Headache 22 40.7% 2 0
Hepatic enzyme increased 22 40.7% 2 0
Hyperhidrosis 22 40.7% 2 0
Hypertension 22 40.7% 2 0
Immunodeficiency 22 40.7% 2 0
Infusion related reaction 22 40.7% 2 0
Joint swelling 22 40.7% 2 0
Pain 22 40.7% 2 0
Product use issue 22 40.7% 2 0
Exposure during pregnancy 21 38.9% 2 0
Intentional product misuse 21 38.9% 2 0
Off label use 21 38.9% 2 0
Overdose 21 38.9% 2 0
Prescribed overdose 21 38.9% 2 0
Wheezing 20 37.0% 0 17
Dyspnoea 18 33.3% 0 16
Productive cough 17 31.5% 0 14

Who Reports ALBUTEROL\GUAIFENESIN Side Effects? Age & Gender Data

Gender: 52.9% female, 47.1% male. Average age: 51.9 years. Most reports from: CA. View detailed demographics →

Is ALBUTEROL\GUAIFENESIN Getting Safer? Reports by Year

YearReportsDeathsHosp.
2009 1 0 0
2015 1 0 1
2019 1 0 0
2024 1 0 0

View full timeline →

What Is ALBUTEROL\GUAIFENESIN Used For?

IndicationReports
Product used for unknown indication 49

Official FDA Label for ALBUTEROL\GUAIFENESIN

Official prescribing information from the FDA-approved drug label.