951 reports of this reaction
2.6% of all VALPROATE SODIUM reports
#5 most reported adverse reaction
SOMNOLENCE is the #5 most commonly reported adverse reaction for VALPROATE SODIUM, manufactured by Fresenius Kabi USA, LLC. There are 951 FDA adverse event reports linking VALPROATE SODIUM to SOMNOLENCE. This represents approximately 2.6% of all 37,274 adverse event reports for this drug.
Patients taking VALPROATE SODIUM who experience somnolence should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
SOMNOLENCE is a less commonly reported adverse event for VALPROATE SODIUM, but still significant enough to appear in the safety profile.
In addition to somnolence, the following adverse reactions have been reported for VALPROATE SODIUM:
The following drugs have also been linked to somnolence in FDA adverse event reports:
SOMNOLENCE has been reported as an adverse event in 951 FDA reports for VALPROATE SODIUM. This does not prove causation, but indicates an association observed in post-market surveillance data.
SOMNOLENCE accounts for approximately 2.6% of all adverse event reports for VALPROATE SODIUM, making it a notable side effect.
If you experience somnolence while taking VALPROATE 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.