1,729 reports of this reaction
2.0% of all DIVALPROEX SODIUM reports
#10 most reported adverse reaction
FALL is the #10 most commonly reported adverse reaction for DIVALPROEX SODIUM, manufactured by AbbVie Inc.. There are 1,729 FDA adverse event reports linking DIVALPROEX SODIUM to FALL. This represents approximately 2.0% of all 87,440 adverse event reports for this drug.
Patients taking DIVALPROEX SODIUM who experience fall should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
FALL is a less commonly reported adverse event for DIVALPROEX SODIUM, but still significant enough to appear in the safety profile.
In addition to fall, the following adverse reactions have been reported for DIVALPROEX SODIUM:
The following drugs have also been linked to fall in FDA adverse event reports:
FALL has been reported as an adverse event in 1,729 FDA reports for DIVALPROEX SODIUM. This does not prove causation, but indicates an association observed in post-market surveillance data.
FALL accounts for approximately 2.0% of all adverse event reports for DIVALPROEX SODIUM, making it a notable side effect.
If you experience fall while taking DIVALPROEX SODIUM, 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.