Does VENLAFAXINE Cause Product administration error? 69 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 69 reports of Product administration error have been filed in association with VENLAFAXINE (Venlafaxine Hydrochloride). This represents 0.1% of all adverse event reports for VENLAFAXINE.
69
Reports of Product administration error with VENLAFAXINE
0.1%
of all VENLAFAXINE reports
5
Deaths
42
Hospitalizations
How Dangerous Is Product administration error From VENLAFAXINE?
Of the 69 reports, 5 (7.2%) resulted in death, 42 (60.9%) required hospitalization, and 9 (13.0%) 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 VENLAFAXINE. However, 69 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 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 VENLAFAXINE Alternatives Have Lower Product administration error Risk?
VENLAFAXINE vs VENTAVIS
VENLAFAXINE vs VENTOLIN
VENLAFAXINE vs VENTOLIN HFA
VENLAFAXINE vs VERAPAMIL
VENLAFAXINE vs VERICIGUAT