156 reports of this reaction
3.2% of all PRUCALOPRIDE reports
#5 most reported adverse reaction
DIARRHOEA is the #5 most commonly reported adverse reaction for PRUCALOPRIDE, manufactured by Takeda Pharmaceuticals America, Inc.. There are 156 FDA adverse event reports linking PRUCALOPRIDE to DIARRHOEA. This represents approximately 3.2% of all 4,835 adverse event reports for this drug.
Patients taking PRUCALOPRIDE 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 PRUCALOPRIDE users, representing a notable but not dominant share of adverse events.
In addition to diarrhoea, the following adverse reactions have been reported for PRUCALOPRIDE:
The following drugs have also been linked to diarrhoea in FDA adverse event reports:
DIARRHOEA has been reported as an adverse event in 156 FDA reports for PRUCALOPRIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIARRHOEA accounts for approximately 3.2% of all adverse event reports for PRUCALOPRIDE, making it a notable side effect.
If you experience diarrhoea while taking PRUCALOPRIDE, 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.