Does TRIHEXYPHENIDYL Cause Product administration error? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Product administration error have been filed in association with TRIHEXYPHENIDYL (Trihexyphenidyl Hydrochloride). This represents 1.2% of all adverse event reports for TRIHEXYPHENIDYL.
21
Reports of Product administration error with TRIHEXYPHENIDYL
1.2%
of all TRIHEXYPHENIDYL reports
0
Deaths
8
Hospitalizations
How Dangerous Is Product administration error From TRIHEXYPHENIDYL?
Of the 21 reports, 8 (38.1%) 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 TRIHEXYPHENIDYL. However, 21 reports have been filed with the FAERS database.
What Other Side Effects Does TRIHEXYPHENIDYL Cause?
Drug ineffective (186)
Off label use (168)
Toxicity to various agents (134)
Somnolence (132)
Coma (123)
Drug abuse (100)
Confusional state (88)
Nausea (76)
Dystonia (68)
Respiratory failure (66)
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 TRIHEXYPHENIDYL Alternatives Have Lower Product administration error Risk?
TRIHEXYPHENIDYL vs TRILACICLIB
TRIHEXYPHENIDYL vs TRILEPTAL
TRIHEXYPHENIDYL vs TRIMEBUTINE
TRIHEXYPHENIDYL vs TRIMEPRAZINE
TRIHEXYPHENIDYL vs TRIMETAZIDINE