Does DITIOCARB Cause Product dose omission issue? 42 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 42 reports of Product dose omission issue have been filed in association with DITIOCARB. This represents 95.5% of all adverse event reports for DITIOCARB.
42
Reports of Product dose omission issue with DITIOCARB
95.5%
of all DITIOCARB reports
32
Deaths
40
Hospitalizations
How Dangerous Is Product dose omission issue From DITIOCARB?
Of the 42 reports, 32 (76.2%) resulted in death, 40 (95.2%) required hospitalization, and 30 (71.4%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DITIOCARB. However, 42 reports have been filed with the FAERS database.
What Other Side Effects Does DITIOCARB Cause?
Arthropathy (42)
Lower respiratory tract infection (42)
Pulmonary pain (42)
Abdominal discomfort (41)
Off label use (41)
Rash (41)
Drug abuse (38)
Overdose (38)
Intentional product misuse (37)
Knee arthroplasty (33)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)