Does ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL Cause Adverse event? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Adverse event have been filed in association with ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL. This represents 51.9% of all adverse event reports for ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL.
14
Reports of Adverse event with ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL
51.9%
of all ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL reports
14
Deaths
14
Hospitalizations
How Dangerous Is Adverse event From ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL?
Of the 14 reports, 14 (100.0%) resulted in death, 14 (100.0%) required hospitalization, and 5 (35.7%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL Cause?
Off label use (24)
Condition aggravated (22)
Drug ineffective (18)
Drug intolerance (18)
Helicobacter infection (18)
Hypertension (18)
Type 2 diabetes mellitus (18)
Hypoaesthesia (17)
Intentional product use issue (17)
Abdominal discomfort (16)
What Other Drugs Cause Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)