Does VENLAFAXINE Cause Incorrect product administration duration? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Incorrect product administration duration have been filed in association with VENLAFAXINE (Venlafaxine Hydrochloride). This represents 0.0% of all adverse event reports for VENLAFAXINE.
8
Reports of Incorrect product administration duration with VENLAFAXINE
0.0%
of all VENLAFAXINE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Incorrect product administration duration From VENLAFAXINE?
Of the 8 reports, 4 (50.0%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VENLAFAXINE. However, 8 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which VENLAFAXINE Alternatives Have Lower Incorrect product administration duration Risk?
VENLAFAXINE vs VENTAVIS
VENLAFAXINE vs VENTOLIN
VENLAFAXINE vs VENTOLIN HFA
VENLAFAXINE vs VERAPAMIL
VENLAFAXINE vs VERICIGUAT