4,294 reports of this reaction
1.6% of all CORTISONE ACETATE reports
#18 most reported adverse reaction
PERICARDITIS is the #18 most commonly reported adverse reaction for CORTISONE ACETATE, manufactured by Boiron. There are 4,294 FDA adverse event reports linking CORTISONE ACETATE to PERICARDITIS. This represents approximately 1.6% of all 272,029 adverse event reports for this drug.
Patients taking CORTISONE ACETATE who experience pericarditis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PERICARDITIS is a less commonly reported adverse event for CORTISONE ACETATE, but still significant enough to appear in the safety profile.
In addition to pericarditis, the following adverse reactions have been reported for CORTISONE ACETATE:
The following drugs have also been linked to pericarditis in FDA adverse event reports:
PERICARDITIS has been reported as an adverse event in 4,294 FDA reports for CORTISONE ACETATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
PERICARDITIS accounts for approximately 1.6% of all adverse event reports for CORTISONE ACETATE, making it a notable side effect.
If you experience pericarditis 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.