4,303 reports of this reaction
1.6% of all CORTISONE ACETATE reports
#17 most reported adverse reaction
SYNOVITIS is the #17 most commonly reported adverse reaction for CORTISONE ACETATE, manufactured by Boiron. There are 4,303 FDA adverse event reports linking CORTISONE ACETATE to SYNOVITIS. This represents approximately 1.6% of all 272,029 adverse event reports for this drug.
Patients taking CORTISONE ACETATE 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 CORTISONE ACETATE, but still significant enough to appear in the safety profile.
In addition to synovitis, the following adverse reactions have been reported for CORTISONE ACETATE:
The following drugs have also been linked to synovitis in FDA adverse event reports:
SYNOVITIS has been reported as an adverse event in 4,303 FDA reports for CORTISONE ACETATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
SYNOVITIS accounts for approximately 1.6% of all adverse event reports for CORTISONE ACETATE, making it a notable side effect.
If you experience synovitis while taking CORTISONE ACETATE, 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.