82/100 · Critical
58,040 FDA adverse event reports
PROCHLORPERAZINE is manufactured by Padagis US LLC and is tracked in the FDA Adverse Event Reporting System (FAERS). There are 58,040 adverse event reports for PROCHLORPERAZINE in the FDA database. Based on our AI analysis, PROCHLORPERAZINE has a safety score of 82 out of 100.
This page focuses specifically on PROCHLORPERAZINE as manufactured by Padagis US LLC, providing safety context within the manufacturer's broader drug portfolio. Different manufacturers of the same active ingredient may have different adverse event profiles due to variations in formulation, inactive ingredients, manufacturing processes, and patient populations.
The following adverse reactions have been most frequently reported for PROCHLORPERAZINE manufactured by Padagis US LLC:
Out of 26,597 classified reports for PROCHLORPERAZINE:
Explore other medications manufactured by Padagis US LLC in the FDA adverse event database:
The most commonly reported side effects of PROCHLORPERAZINE include NAUSEA, FATIGUE, DIARRHOEA. These are based on 58,040 FDA adverse event reports.
PROCHLORPERAZINE has a safety score of 82/100 based on AI analysis of FDA adverse event reports. Always discuss medication risks with your healthcare provider.