DIVALPROEX SODIUM and ANXIETY

Overview

ANXIETY is the #11 most commonly reported adverse reaction for DIVALPROEX SODIUM, manufactured by AbbVie Inc.. There are 1,692 FDA adverse event reports linking DIVALPROEX SODIUM to ANXIETY. This represents approximately 1.9% of all 87,440 adverse event reports for this drug.

Patients taking DIVALPROEX SODIUM who experience anxiety should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.

Reporting Frequency

ANXIETY is a less commonly reported adverse event for DIVALPROEX SODIUM, but still significant enough to appear in the safety profile.

Other Side Effects of DIVALPROEX SODIUM

In addition to anxiety, the following adverse reactions have been reported for DIVALPROEX SODIUM:

• DRUG INEFFECTIVE — 2,976 reports
• SEIZURE — 2,499 reports
• WEIGHT INCREASED — 2,137 reports
• NAUSEA — 2,042 reports
• OFF LABEL USE — 1,970 reports
• FATIGUE — 1,901 reports
• PAIN — 1,873 reports
• SOMNOLENCE — 1,837 reports
• TREMOR — 1,796 reports
• FALL — 1,729 reports

Other Drugs Associated with ANXIETY

The following drugs have also been linked to anxiety in FDA adverse event reports:

Does DIVALPROEX SODIUM cause ANXIETY?

ANXIETY has been reported as an adverse event in 1,692 FDA reports for DIVALPROEX SODIUM. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is ANXIETY with DIVALPROEX SODIUM?

ANXIETY accounts for approximately 1.9% of all adverse event reports for DIVALPROEX SODIUM, making it a notable side effect.

What should I do if I experience ANXIETY while taking DIVALPROEX SODIUM?

If you experience anxiety 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.

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