Does VENLAFAXINE Cause Wrong patient received product? 38 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 38 reports of Wrong patient received product have been filed in association with VENLAFAXINE (Venlafaxine Hydrochloride). This represents 0.1% of all adverse event reports for VENLAFAXINE.
38
Reports of Wrong patient received product with VENLAFAXINE
0.1%
of all VENLAFAXINE reports
9
Deaths
17
Hospitalizations
How Dangerous Is Wrong patient received product From VENLAFAXINE?
Of the 38 reports, 9 (23.7%) resulted in death, 17 (44.7%) required hospitalization, and 9 (23.7%) 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 VENLAFAXINE. However, 38 reports have been filed with the FAERS database.
What Other Side Effects Does VENLAFAXINE Cause?
Drug ineffective (5,408)
Toxicity to various agents (3,917)
Nausea (2,989)
Completed suicide (2,929)
Headache (2,668)
Dizziness (2,426)
Off label use (2,310)
Overdose (2,220)
Intentional overdose (2,187)
Fatigue (2,153)
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 VENLAFAXINE Alternatives Have Lower Wrong patient received product Risk?
VENLAFAXINE vs VENTAVIS
VENLAFAXINE vs VENTOLIN
VENLAFAXINE vs VENTOLIN HFA
VENLAFAXINE vs VERAPAMIL
VENLAFAXINE vs VERICIGUAT