ANXIETY is the #2 most commonly reported adverse reaction for SODIUM OXYBATE, manufactured by Jazz Pharmaceuticals, Inc.. There are 3,934 FDA adverse event reports linking SODIUM OXYBATE to ANXIETY. This represents approximately 3.1% of all 126,117 adverse event reports for this drug.
SODIUM OXYBATE has an overall safety score of 85 out of 100. Patients taking SODIUM OXYBATE 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
ANXIETY3,934 of 126,117 reports
ANXIETY is moderately reported among SODIUM OXYBATE users, representing a notable but not dominant share of adverse events.
Other Side Effects of SODIUM OXYBATE
In addition to anxiety, the following adverse reactions have been reported for SODIUM OXYBATE:
ANXIETY has been reported as an adverse event in 3,934 FDA reports for SODIUM OXYBATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is ANXIETY with SODIUM OXYBATE?
ANXIETY accounts for approximately 3.1% of all adverse event reports for SODIUM OXYBATE, making it one of the most commonly reported side effect.
What should I do if I experience ANXIETY while taking SODIUM OXYBATE?
If you experience anxiety while taking SODIUM OXYBATE, 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.
Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.