2,976 reports of this reaction
3.4% of all DIVALPROEX SODIUM reports
#1 most reported adverse reaction
DRUG INEFFECTIVE is the #1 most commonly reported adverse reaction for DIVALPROEX SODIUM, manufactured by AbbVie Inc.. There are 2,976 FDA adverse event reports linking DIVALPROEX SODIUM to DRUG INEFFECTIVE. This represents approximately 3.4% of all 87,440 adverse event reports for this drug.
Patients taking DIVALPROEX SODIUM who experience drug ineffective should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DRUG INEFFECTIVE is moderately reported among DIVALPROEX SODIUM users, representing a notable but not dominant share of adverse events.
In addition to drug ineffective, the following adverse reactions have been reported for DIVALPROEX SODIUM:
The following drugs have also been linked to drug ineffective in FDA adverse event reports:
DRUG INEFFECTIVE has been reported as an adverse event in 2,976 FDA reports for DIVALPROEX SODIUM. This does not prove causation, but indicates an association observed in post-market surveillance data.
DRUG INEFFECTIVE accounts for approximately 3.4% of all adverse event reports for DIVALPROEX SODIUM, making it one of the most commonly reported side effect.
If you experience drug ineffective 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.