41 reports of this reaction
2.2% of all CEFPODOXIME PROXETIL reports
#7 most reported adverse reaction
NAUSEA is the #7 most commonly reported adverse reaction for CEFPODOXIME PROXETIL, manufactured by Amici Pharmaceuticals, LLC.. There are 41 FDA adverse event reports linking CEFPODOXIME PROXETIL to NAUSEA. This represents approximately 2.2% of all 1,861 adverse event reports for this drug.
Patients taking CEFPODOXIME PROXETIL 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 CEFPODOXIME PROXETIL, but still significant enough to appear in the safety profile.
In addition to nausea, the following adverse reactions have been reported for CEFPODOXIME PROXETIL:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 41 FDA reports for CEFPODOXIME PROXETIL. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 2.2% of all adverse event reports for CEFPODOXIME PROXETIL, making it a notable side effect.
If you experience nausea while taking CEFPODOXIME PROXETIL, 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.