574 reports of this reaction
2.3% of all CEFUROXIME reports
#7 most reported adverse reaction
DIARRHOEA is the #7 most commonly reported adverse reaction for CEFUROXIME, manufactured by Hikma Pharmaceuticals USA Inc.. There are 574 FDA adverse event reports linking CEFUROXIME to DIARRHOEA. This represents approximately 2.3% of all 25,003 adverse event reports for this drug.
Patients taking CEFUROXIME who experience diarrhoea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DIARRHOEA is a less commonly reported adverse event for CEFUROXIME, but still significant enough to appear in the safety profile.
In addition to diarrhoea, the following adverse reactions have been reported for CEFUROXIME:
The following drugs have also been linked to diarrhoea in FDA adverse event reports:
DIARRHOEA has been reported as an adverse event in 574 FDA reports for CEFUROXIME. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIARRHOEA accounts for approximately 2.3% of all adverse event reports for CEFUROXIME, making it a notable side effect.
If you experience diarrhoea while taking CEFUROXIME, 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.