Does BUFEXAMAC Cause Intentional product misuse? 26 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Intentional product misuse have been filed in association with BUFEXAMAC. This represents 46.4% of all adverse event reports for BUFEXAMAC.
26
Reports of Intentional product misuse with BUFEXAMAC
46.4%
of all BUFEXAMAC reports
26
Deaths
24
Hospitalizations
How Dangerous Is Intentional product misuse From BUFEXAMAC?
Of the 26 reports, 26 (100.0%) resulted in death, 24 (92.3%) required hospitalization, and 25 (96.2%) 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. However, 26 reports have been filed with the FAERS database.
What Other Side Effects Does BUFEXAMAC Cause?
Abdominal distension (33)
Vomiting (32)
Abdominal pain (30)
Appendicitis (30)
Appendicolith (30)
Ascites (30)
Condition aggravated (30)
Dyspnoea (30)
Somnolence (30)
Blood phosphorus increased (29)
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)