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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\CYANOCOBALAMIN\THIAMINE\TRAMADOL: 27 Adverse Event Reports & Safety Profile

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27
Total FAERS Reports
24 (88.9%)
Deaths Reported
20
Hospitalizations
27
As Primary/Secondary Suspect
8
Life-Threatening
7
Disabilities

Active Ingredient: ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL HYDROCHLORIDE ·

What Are the Most Common ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL Side Effects?

#1 Most Reported
Off label use
24 reports (88.9%)
#2 Most Reported
Condition aggravated
22 reports (81.5%)
#3 Most Reported
Type 2 diabetes mellitus
18 reports (66.7%)

All ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Off label use 24 88.9% 23 17
Condition aggravated 22 81.5% 21 15
Drug ineffective 18 66.7% 17 18
Drug intolerance 18 66.7% 17 18
Helicobacter infection 18 66.7% 17 18
Hypertension 18 66.7% 17 18
Type 2 diabetes mellitus 18 66.7% 17 18
Hypoaesthesia 17 63.0% 17 17
Intentional product use issue 17 63.0% 16 17
Abdominal discomfort 16 59.3% 15 16
Alopecia 16 59.3% 15 16
Arthralgia 16 59.3% 15 16
Blood cholesterol increased 16 59.3% 15 16
Dizziness 16 59.3% 15 16
Fatigue 16 59.3% 15 16
Fibromyalgia 16 59.3% 15 16
General physical health deterioration 16 59.3% 15 16
Headache 16 59.3% 15 16
Hepatic enzyme increased 16 59.3% 15 16
Infusion related reaction 16 59.3% 15 16

Who Reports ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL Side Effects? Age & Gender Data

Gender: 100.0% female, 0.0% male. Average age: 43.6 years. Most reports from: CA. View detailed demographics →

What Is ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL Used For?

IndicationReports
Product used for unknown indication 25

Official FDA Label for ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL

Official prescribing information from the FDA-approved drug label.