ANXIETY is the #24 most commonly reported adverse reaction for PROCHLORPERAZINE, manufactured by Padagis US LLC. There are 695 FDA adverse event reports linking PROCHLORPERAZINE to ANXIETY. This represents approximately 1.2% of all 58,040 adverse event reports for this drug.
PROCHLORPERAZINE has an overall safety score of 82 out of 100. Patients taking PROCHLORPERAZINE 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
ANXIETY695 of 58,040 reports
ANXIETY is a less commonly reported adverse event for PROCHLORPERAZINE, but still significant enough to appear in the safety profile.
Other Side Effects of PROCHLORPERAZINE
In addition to anxiety, the following adverse reactions have been reported for PROCHLORPERAZINE:
ANXIETY has been reported as an adverse event in 695 FDA reports for PROCHLORPERAZINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
How common is ANXIETY with PROCHLORPERAZINE?
ANXIETY accounts for approximately 1.2% of all adverse event reports for PROCHLORPERAZINE, making it a notable side effect.
What should I do if I experience ANXIETY while taking PROCHLORPERAZINE?
If you experience anxiety while taking PROCHLORPERAZINE, 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.