Does DITIOCARB Cause Intentional product misuse? 37 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 37 reports of Intentional product misuse have been filed in association with DITIOCARB. This represents 84.1% of all adverse event reports for DITIOCARB.
37
Reports of Intentional product misuse with DITIOCARB
84.1%
of all DITIOCARB reports
28
Deaths
36
Hospitalizations
How Dangerous Is Intentional product misuse From DITIOCARB?
Of the 37 reports, 28 (75.7%) resulted in death, 36 (97.3%) required hospitalization, and 27 (73.0%) 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 DITIOCARB. However, 37 reports have been filed with the FAERS database.
What Other Side Effects Does DITIOCARB Cause?
Arthropathy (42)
Lower respiratory tract infection (42)
Product dose omission issue (42)
Pulmonary pain (42)
Abdominal discomfort (41)
Off label use (41)
Rash (41)
Drug abuse (38)
Overdose (38)
Knee arthroplasty (33)
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)