Does DITIOCARB Cause Condition aggravated? 31 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Condition aggravated have been filed in association with DITIOCARB. This represents 70.5% of all adverse event reports for DITIOCARB.
31
Reports of Condition aggravated with DITIOCARB
70.5%
of all DITIOCARB reports
31
Deaths
29
Hospitalizations
How Dangerous Is Condition aggravated From DITIOCARB?
Of the 31 reports, 31 (100.0%) resulted in death, 29 (93.5%) required hospitalization, and 29 (93.5%) 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 DITIOCARB. However, 31 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)
Intentional product misuse (37)
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)