3,026 reports of this reaction
2.0% of all VENLAFAXINE reports
#9 most reported adverse reaction
DIZZINESS is the #9 most commonly reported adverse reaction for VENLAFAXINE, manufactured by Alembic Pharmaceuticals Inc.. There are 3,026 FDA adverse event reports linking VENLAFAXINE to DIZZINESS. This represents approximately 2.0% of all 151,835 adverse event reports for this drug.
VENLAFAXINE has an overall safety score of 88 out of 100. Patients taking VENLAFAXINE who experience dizziness should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DIZZINESS is a less commonly reported adverse event for VENLAFAXINE, but still significant enough to appear in the safety profile.
In addition to dizziness, the following adverse reactions have been reported for VENLAFAXINE:
The following drugs have also been linked to dizziness in FDA adverse event reports:
DIZZINESS has been reported as an adverse event in 3,026 FDA reports for VENLAFAXINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIZZINESS accounts for approximately 2.0% of all adverse event reports for VENLAFAXINE, making it a notable side effect.
If you experience dizziness while taking VENLAFAXINE, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.