Does ZUCLOPENTHIXOL 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 ZUCLOPENTHIXOL. This represents 0.5% of all adverse event reports for ZUCLOPENTHIXOL.
13
Reports of Product administration error with ZUCLOPENTHIXOL
0.5%
of all ZUCLOPENTHIXOL reports
1
Deaths
12
Hospitalizations
How Dangerous Is Product administration error From ZUCLOPENTHIXOL?
Of the 13 reports, 1 (7.7%) resulted in death, 12 (92.3%) required hospitalization, and 2 (15.4%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZUCLOPENTHIXOL. However, 13 reports have been filed with the FAERS database.
What Other Side Effects Does ZUCLOPENTHIXOL Cause?
Drug ineffective (660)
Dyskinesia (414)
Schizophrenia (409)
Dystonia (404)
Sedation (403)
Sexual dysfunction (394)
Suicide attempt (389)
Blood glucose increased (379)
Anosognosia (374)
Blood prolactin abnormal (374)
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 ZUCLOPENTHIXOL Alternatives Have Lower Product administration error Risk?
ZUCLOPENTHIXOL vs ZUCLOPENTHIXOL DECANOATE
ZUCLOPENTHIXOL vs ZURANOLONE
ZUCLOPENTHIXOL vs ZYPREXA
ZUCLOPENTHIXOL vs ZYTIGA
ZUCLOPENTHIXOL vs ZYVOX