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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\AMBROXOL\GUAIFENESIN: 40 Adverse Event Reports & Safety Profile

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40
Total FAERS Reports
0
Deaths Reported
34
Hospitalizations
40
As Primary/Secondary Suspect
16
Life-Threatening

Active Ingredient: ALBUTEROL SULFATE\AMBROXOL HYDROCHLORIDE\GUAIFENESIN ·

What Are the Most Common ALBUTEROL\AMBROXOL\GUAIFENESIN Side Effects?

#1 Most Reported
Toxicity to various agents
28 reports (70.0%)
#2 Most Reported
Sedation complication
28 reports (70.0%)
#3 Most Reported
Sedation
28 reports (70.0%)

All ALBUTEROL\AMBROXOL\GUAIFENESIN Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Balance disorder 28 70.0% 0 28
Blood calcium decreased 28 70.0% 0 28
Cognitive disorder 28 70.0% 0 28
Constipation 28 70.0% 0 28
Creatinine renal clearance decreased 28 70.0% 0 28
Depressed level of consciousness 28 70.0% 0 28
Fall 28 70.0% 0 28
Hypotension 28 70.0% 0 28
Mobility decreased 28 70.0% 0 28
Orthostatic hypotension 28 70.0% 0 28
Pain 28 70.0% 0 28
Sedation 28 70.0% 0 28
Sedation complication 28 70.0% 0 28
Toxicity to various agents 28 70.0% 0 28
Dyspnoea 23 57.5% 0 20
Multiple drug therapy 16 40.0% 0 16
Drug interaction 15 37.5% 0 15
Renal function test abnormal 15 37.5% 0 15
Asthma 12 30.0% 0 6
Product use in unapproved indication 12 30.0% 0 12

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

Gender: 97.3% female, 2.7% male. Average age: 73.2 years. Most reports from: CA. View detailed demographics →

What Is ALBUTEROL\AMBROXOL\GUAIFENESIN Used For?

IndicationReports
Product used for unknown indication 38

Official FDA Label for ALBUTEROL\AMBROXOL\GUAIFENESIN

Official prescribing information from the FDA-approved drug label.