316 reports of this reaction
0.5% of all PROCHLORPERAZINE reports
#63 most reported adverse reaction
ABDOMINAL DISCOMFORT is the #63 most commonly reported adverse reaction for PROCHLORPERAZINE, manufactured by Padagis US LLC. There are 316 FDA adverse event reports linking PROCHLORPERAZINE to ABDOMINAL DISCOMFORT. This represents approximately 0.5% 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 abdominal discomfort should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ABDOMINAL DISCOMFORT is a less commonly reported adverse event for PROCHLORPERAZINE, but still significant enough to appear in the safety profile.
In addition to abdominal discomfort, the following adverse reactions have been reported for PROCHLORPERAZINE:
The following drugs have also been linked to abdominal discomfort in FDA adverse event reports:
ABDOMINAL DISCOMFORT has been reported as an adverse event in 316 FDA reports for PROCHLORPERAZINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ABDOMINAL DISCOMFORT accounts for approximately 0.5% of all adverse event reports for PROCHLORPERAZINE, making it a notable side effect.
If you experience abdominal discomfort 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.