6,149 reports of this reaction
1.9% of all DICLOFENAC SODIUM 1% reports
#4 most reported adverse reaction
RHEUMATOID ARTHRITIS is the #4 most commonly reported adverse reaction for DICLOFENAC SODIUM 1%, manufactured by Aurobindo Pharma Limited. There are 6,149 FDA adverse event reports linking DICLOFENAC SODIUM 1% to RHEUMATOID ARTHRITIS. This represents approximately 1.9% of all 323,575 adverse event reports for this drug.
Patients taking DICLOFENAC SODIUM 1% who experience rheumatoid arthritis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
RHEUMATOID ARTHRITIS is a less commonly reported adverse event for DICLOFENAC SODIUM 1%, but still significant enough to appear in the safety profile.
In addition to rheumatoid arthritis, the following adverse reactions have been reported for DICLOFENAC SODIUM 1%:
The following drugs have also been linked to rheumatoid arthritis in FDA adverse event reports:
RHEUMATOID ARTHRITIS has been reported as an adverse event in 6,149 FDA reports for DICLOFENAC SODIUM 1%. This does not prove causation, but indicates an association observed in post-market surveillance data.
RHEUMATOID ARTHRITIS accounts for approximately 1.9% of all adverse event reports for DICLOFENAC SODIUM 1%, making it a notable side effect.
If you experience rheumatoid arthritis while taking DICLOFENAC SODIUM 1%, 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.