2,021 reports of this reaction
1.3% of all DICLOFENAC POTASSIUM, FILM COATED reports
#11 most reported adverse reaction
SYNOVITIS is the #11 most commonly reported adverse reaction for DICLOFENAC POTASSIUM, FILM COATED, manufactured by Advagen Pharma Ltd. There are 2,021 FDA adverse event reports linking DICLOFENAC POTASSIUM, FILM COATED to SYNOVITIS. This represents approximately 1.3% of all 153,821 adverse event reports for this drug.
Patients taking DICLOFENAC POTASSIUM, FILM COATED who experience synovitis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
SYNOVITIS is a less commonly reported adverse event for DICLOFENAC POTASSIUM, FILM COATED, but still significant enough to appear in the safety profile.
In addition to synovitis, the following adverse reactions have been reported for DICLOFENAC POTASSIUM, FILM COATED:
The following drugs have also been linked to synovitis in FDA adverse event reports:
SYNOVITIS has been reported as an adverse event in 2,021 FDA reports for DICLOFENAC POTASSIUM, FILM COATED. This does not prove causation, but indicates an association observed in post-market surveillance data.
SYNOVITIS accounts for approximately 1.3% of all adverse event reports for DICLOFENAC POTASSIUM, FILM COATED, making it a notable side effect.
If you experience synovitis while taking DICLOFENAC POTASSIUM, FILM COATED, 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.