12,871 reports of this reaction
2.2% of all DICLOFENAC SODIUM reports
#3 most reported adverse reaction
FATIGUE is the #3 most commonly reported adverse reaction for DICLOFENAC SODIUM, manufactured by Haleon US Holdings LLC. There are 12,871 FDA adverse event reports linking DICLOFENAC SODIUM to FATIGUE. This represents approximately 2.2% of all 574,671 adverse event reports for this drug.
Patients taking DICLOFENAC SODIUM who experience fatigue should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
FATIGUE is a less commonly reported adverse event for DICLOFENAC SODIUM, but still significant enough to appear in the safety profile.
In addition to fatigue, the following adverse reactions have been reported for DICLOFENAC SODIUM:
The following drugs have also been linked to fatigue in FDA adverse event reports:
FATIGUE has been reported as an adverse event in 12,871 FDA reports for DICLOFENAC SODIUM. This does not prove causation, but indicates an association observed in post-market surveillance data.
FATIGUE accounts for approximately 2.2% of all adverse event reports for DICLOFENAC SODIUM, making it one of the most commonly reported side effect.
If you experience fatigue 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.