Does BUFEXAMAC\LIDOCAINE Cause Intentional product misuse? 33 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 33 reports of Intentional product misuse have been filed in association with BUFEXAMAC\LIDOCAINE. This represents 67.4% of all adverse event reports for BUFEXAMAC\LIDOCAINE.
33
Reports of Intentional product misuse with BUFEXAMAC\LIDOCAINE
67.4%
of all BUFEXAMAC\LIDOCAINE reports
33
Deaths
30
Hospitalizations
How Dangerous Is Intentional product misuse From BUFEXAMAC\LIDOCAINE?
Of the 33 reports, 33 (100.0%) resulted in death, 30 (90.9%) required hospitalization, and 28 (84.8%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BUFEXAMAC\LIDOCAINE. However, 33 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)