Does BUFEXAMAC\LIDOCAINE Cause Condition aggravated? 39 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 39 reports of Condition aggravated have been filed in association with BUFEXAMAC\LIDOCAINE. This represents 79.6% of all adverse event reports for BUFEXAMAC\LIDOCAINE.
39
Reports of Condition aggravated with BUFEXAMAC\LIDOCAINE
79.6%
of all BUFEXAMAC\LIDOCAINE reports
39
Deaths
36
Hospitalizations
How Dangerous Is Condition aggravated From BUFEXAMAC\LIDOCAINE?
Of the 39 reports, 39 (100.0%) resulted in death, 36 (92.3%) required hospitalization, and 28 (71.8%) 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 BUFEXAMAC\LIDOCAINE. However, 39 reports have been filed with the FAERS database.
What Other Side Effects Does BUFEXAMAC\LIDOCAINE Cause?
Abdominal distension (43)
Vomiting (42)
Stress (41)
Abdominal pain (40)
Appendicitis (40)
Appendicolith (40)
Ascites (40)
Hyponatraemia (40)
Off label use (40)
Ventricular fibrillation (40)
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)