2,360 reports of this reaction
1.6% of all MESALAMINE reports
#17 most reported adverse reaction
FREQUENT BOWEL MOVEMENTS is the #17 most commonly reported adverse reaction for MESALAMINE, manufactured by Takeda Pharmaceuticals America, Inc.. There are 2,360 FDA adverse event reports linking MESALAMINE to FREQUENT BOWEL MOVEMENTS. This represents approximately 1.6% of all 145,688 adverse event reports for this drug.
Patients taking MESALAMINE who experience frequent bowel movements should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
FREQUENT BOWEL MOVEMENTS is a less commonly reported adverse event for MESALAMINE, but still significant enough to appear in the safety profile.
In addition to frequent bowel movements, the following adverse reactions have been reported for MESALAMINE:
The following drugs have also been linked to frequent bowel movements in FDA adverse event reports:
FREQUENT BOWEL MOVEMENTS has been reported as an adverse event in 2,360 FDA reports for MESALAMINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
FREQUENT BOWEL MOVEMENTS accounts for approximately 1.6% of all adverse event reports for MESALAMINE, making it a notable side effect.
If you experience frequent bowel movements while taking MESALAMINE, 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.