5,060 reports of this reaction
3.6% of all BORTEZOMIB reports
#4 most reported adverse reaction
DIARRHOEA is the #4 most commonly reported adverse reaction for BORTEZOMIB, manufactured by Takeda Pharmaceuticals America, Inc.. There are 5,060 FDA adverse event reports linking BORTEZOMIB to DIARRHOEA. This represents approximately 3.6% of all 141,037 adverse event reports for this drug.
Patients taking BORTEZOMIB 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 BORTEZOMIB users, representing a notable but not dominant share of adverse events.
In addition to diarrhoea, the following adverse reactions have been reported for BORTEZOMIB:
The following drugs have also been linked to diarrhoea in FDA adverse event reports:
DIARRHOEA has been reported as an adverse event in 5,060 FDA reports for BORTEZOMIB. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIARRHOEA accounts for approximately 3.6% of all adverse event reports for BORTEZOMIB, making it a notable side effect.
If you experience diarrhoea while taking BORTEZOMIB, 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.