Does CLORAZEPATE Cause Product administration error? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product administration error have been filed in association with CLORAZEPATE (Clorazepate Dipotassium). This represents 0.7% of all adverse event reports for CLORAZEPATE.
13
Reports of Product administration error with CLORAZEPATE
0.7%
of all CLORAZEPATE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Product administration error From CLORAZEPATE?
Of the 13 reports, 4 (30.8%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CLORAZEPATE. However, 13 reports have been filed with the FAERS database.
What Other Side Effects Does CLORAZEPATE Cause?
Coma (203)
Toxicity to various agents (173)
Somnolence (142)
Off label use (109)
Drug abuse (98)
Hypotension (96)
Intentional overdose (94)
Drug ineffective (92)
Fall (92)
Anxiety (78)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which CLORAZEPATE Alternatives Have Lower Product administration error Risk?
CLORAZEPATE vs CLOSTRIDIUM TETANI TOXOID ANTIGEN
CLORAZEPATE vs CLOTHIAPINE
CLORAZEPATE vs CLOTIAZEPAM
CLORAZEPATE vs CLOTRIMAZOLE
CLORAZEPATE vs CLOXACILLIN