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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DITIOCARB Cause Off label use? 41 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 41 reports of Off label use have been filed in association with DITIOCARB. This represents 93.2% of all adverse event reports for DITIOCARB.

41
Reports of Off label use with DITIOCARB
93.2%
of all DITIOCARB reports
32
Deaths
39
Hospitalizations

How Dangerous Is Off label use From DITIOCARB?

Of the 41 reports, 32 (78.0%) resulted in death, 39 (95.1%) required hospitalization, and 30 (73.2%) were considered life-threatening.

Is Off label use Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DITIOCARB. However, 41 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) Rash (41) Drug abuse (38) Overdose (38) Intentional product misuse (37) Knee arthroplasty (33)

What Other Drugs Cause Off label use?

RITUXIMAB (39,751) INFLIXIMAB (34,801) DENOSUMAB (34,612) METHOTREXATE (24,020) VEDOLIZUMAB (21,017) ETANERCEPT (20,178) TOCILIZUMAB (18,256) PREDNISONE (17,867) LENALIDOMIDE (17,017) ADALIMUMAB (16,417)

Related Pages

DITIOCARB Full Profile All Off label use Reports All Drugs Causing Off label use DITIOCARB Demographics