Does ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL Cause Condition aggravated? 22 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Condition aggravated have been filed in association with ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL. This represents 81.5% of all adverse event reports for ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL.
22
Reports of Condition aggravated with ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL
81.5%
of all ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL reports
21
Deaths
15
Hospitalizations
How Dangerous Is Condition aggravated From ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL?
Of the 22 reports, 21 (95.5%) resulted in death, 15 (68.2%) required hospitalization, and 6 (27.3%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL. However, 22 reports have been filed with the FAERS database.
What Other Side Effects Does ACETAMINOPHEN\CYANOCOBALAMIN\THIAMINE\TRAMADOL Cause?
Off label use (24)
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)
Alopecia (16)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)