10,032 reports of this reaction
2.4% of all PANTOPRAZOLE SODIUM reports
#5 most reported adverse reaction
NAUSEA is the #5 most commonly reported adverse reaction for PANTOPRAZOLE SODIUM, manufactured by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.. There are 10,032 FDA adverse event reports linking PANTOPRAZOLE SODIUM to NAUSEA. This represents approximately 2.4% of all 411,823 adverse event reports for this drug.
PANTOPRAZOLE SODIUM has an overall safety score of 85 out of 100. Patients taking PANTOPRAZOLE SODIUM who experience nausea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NAUSEA is a less commonly reported adverse event for PANTOPRAZOLE SODIUM, but still significant enough to appear in the safety profile.
In addition to nausea, the following adverse reactions have been reported for PANTOPRAZOLE SODIUM:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 10,032 FDA reports for PANTOPRAZOLE SODIUM. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 2.4% of all adverse event reports for PANTOPRAZOLE SODIUM, making it a notable side effect.
If you experience nausea while taking PANTOPRAZOLE 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.