3,744 reports of this reaction
2.7% of all POMALIDOMIDE reports
#6 most reported adverse reaction
DIARRHOEA is the #6 most commonly reported adverse reaction for POMALIDOMIDE, manufactured by Celgene Corporation. There are 3,744 FDA adverse event reports linking POMALIDOMIDE to DIARRHOEA. This represents approximately 2.7% of all 136,988 adverse event reports for this drug.
POMALIDOMIDE has an overall safety score of 88 out of 100. Patients taking POMALIDOMIDE 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 POMALIDOMIDE, but still significant enough to appear in the safety profile.
In addition to diarrhoea, the following adverse reactions have been reported for POMALIDOMIDE:
The following drugs have also been linked to diarrhoea in FDA adverse event reports:
DIARRHOEA has been reported as an adverse event in 3,744 FDA reports for POMALIDOMIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIARRHOEA accounts for approximately 2.7% of all adverse event reports for POMALIDOMIDE, making it a notable side effect.
If you experience diarrhoea while taking POMALIDOMIDE, 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.