Does CLOBAZAM Cause Product dose omission in error? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product dose omission in error have been filed in association with CLOBAZAM (Clobazam). This represents 0.1% of all adverse event reports for CLOBAZAM.
7
Reports of Product dose omission in error with CLOBAZAM
0.1%
of all CLOBAZAM reports
1
Deaths
4
Hospitalizations
How Dangerous Is Product dose omission in error From CLOBAZAM?
Of the 7 reports, 1 (14.3%) resulted in death, 4 (57.1%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CLOBAZAM. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does CLOBAZAM Cause?
Drug ineffective (1,918)
Seizure (1,787)
Off label use (957)
Somnolence (890)
Foetal exposure during pregnancy (531)
Multiple-drug resistance (486)
Epilepsy (464)
Drug interaction (431)
Fatigue (418)
Status epilepticus (366)
What Other Drugs Cause Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which CLOBAZAM Alternatives Have Lower Product dose omission in error Risk?
CLOBAZAM vs CLOBETASOL
CLOBAZAM vs CLOBETASONE
CLOBAZAM vs CLODRONATE
CLOBAZAM vs CLOFARABINE
CLOBAZAM vs CLOFAZIMINE