Does TRIHEXYPHENIDYL Cause Wrong patient received product? 62 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 62 reports of Wrong patient received product have been filed in association with TRIHEXYPHENIDYL (Trihexyphenidyl Hydrochloride). This represents 3.5% of all adverse event reports for TRIHEXYPHENIDYL.
62
Reports of Wrong patient received product with TRIHEXYPHENIDYL
3.5%
of all TRIHEXYPHENIDYL reports
23
Deaths
18
Hospitalizations
How Dangerous Is Wrong patient received product From TRIHEXYPHENIDYL?
Of the 62 reports, 23 (37.1%) resulted in death, 18 (29.0%) required hospitalization, and 8 (12.9%) were considered life-threatening.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TRIHEXYPHENIDYL. However, 62 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 Wrong patient received product?
INSULIN LISPRO (334)
CLOZAPINE (198)
RISPERIDONE (176)
OXAZEPAM (152)
BISOPROLOL (150)
LEVETIRACETAM (126)
ACETAMINOPHEN (123)
METFORMIN (116)
INSULIN GLARGINE (114)
CLONAZEPAM (112)
Which TRIHEXYPHENIDYL Alternatives Have Lower Wrong patient received product Risk?
TRIHEXYPHENIDYL vs TRILACICLIB
TRIHEXYPHENIDYL vs TRILEPTAL
TRIHEXYPHENIDYL vs TRIMEBUTINE
TRIHEXYPHENIDYL vs TRIMEPRAZINE
TRIHEXYPHENIDYL vs TRIMETAZIDINE