9,017 reports of this reaction
1.6% of all DICLOFENAC SODIUM reports
#9 most reported adverse reaction
ABDOMINAL DISCOMFORT is the #9 most commonly reported adverse reaction for DICLOFENAC SODIUM, manufactured by Haleon US Holdings LLC. There are 9,017 FDA adverse event reports linking DICLOFENAC SODIUM to ABDOMINAL DISCOMFORT. This represents approximately 1.6% of all 574,671 adverse event reports for this drug.
Patients taking DICLOFENAC SODIUM who experience abdominal discomfort should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ABDOMINAL DISCOMFORT is a less commonly reported adverse event for DICLOFENAC SODIUM, but still significant enough to appear in the safety profile.
In addition to abdominal discomfort, the following adverse reactions have been reported for DICLOFENAC SODIUM:
The following drugs have also been linked to abdominal discomfort in FDA adverse event reports:
ABDOMINAL DISCOMFORT has been reported as an adverse event in 9,017 FDA reports for DICLOFENAC SODIUM. This does not prove causation, but indicates an association observed in post-market surveillance data.
ABDOMINAL DISCOMFORT accounts for approximately 1.6% of all adverse event reports for DICLOFENAC SODIUM, making it a notable side effect.
If you experience abdominal discomfort while taking DICLOFENAC SODIUM, 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.