Does ZUCLOPENTHIXOL Cause Tardive dyskinesia? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Tardive dyskinesia have been filed in association with ZUCLOPENTHIXOL. This represents 1.2% of all adverse event reports for ZUCLOPENTHIXOL.
28
Reports of Tardive dyskinesia with ZUCLOPENTHIXOL
1.2%
of all ZUCLOPENTHIXOL reports
0
Deaths
4
Hospitalizations
How Dangerous Is Tardive dyskinesia From ZUCLOPENTHIXOL?
Of the 28 reports, 4 (14.3%) required hospitalization, and 1 (3.6%) were considered life-threatening.
Is Tardive dyskinesia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZUCLOPENTHIXOL. However, 28 reports have been filed with the FAERS database.