6,692 reports of this reaction
5.4% of all FLUOROURACIL reports
#1 most reported adverse reaction
DIARRHOEA is the #1 most commonly reported adverse reaction for FLUOROURACIL, manufactured by Bausch Health US, LLC. There are 6,692 FDA adverse event reports linking FLUOROURACIL to DIARRHOEA. This represents approximately 5.4% of all 124,552 adverse event reports for this drug.
Patients taking FLUOROURACIL 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 moderately reported among FLUOROURACIL users, representing a notable but not dominant share of adverse events.
In addition to diarrhoea, the following adverse reactions have been reported for FLUOROURACIL:
The following drugs have also been linked to diarrhoea in FDA adverse event reports:
DIARRHOEA has been reported as an adverse event in 6,692 FDA reports for FLUOROURACIL. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIARRHOEA accounts for approximately 5.4% of all adverse event reports for FLUOROURACIL, making it one of the most commonly reported side effect.
If you experience diarrhoea while taking FLUOROURACIL, 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.