218 reports of this reaction
1.2% of all DRONEDARONE reports
#16 most reported adverse reaction
OEDEMA PERIPHERAL is the #16 most commonly reported adverse reaction for DRONEDARONE, manufactured by Sanofi-Aventis U.S. LLC. There are 218 FDA adverse event reports linking DRONEDARONE to OEDEMA PERIPHERAL. This represents approximately 1.2% of all 17,724 adverse event reports for this drug.
Patients taking DRONEDARONE who experience oedema peripheral should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
OEDEMA PERIPHERAL is a less commonly reported adverse event for DRONEDARONE, but still significant enough to appear in the safety profile.
In addition to oedema peripheral, the following adverse reactions have been reported for DRONEDARONE:
The following drugs have also been linked to oedema peripheral in FDA adverse event reports:
OEDEMA PERIPHERAL has been reported as an adverse event in 218 FDA reports for DRONEDARONE. This does not prove causation, but indicates an association observed in post-market surveillance data.
OEDEMA PERIPHERAL accounts for approximately 1.2% of all adverse event reports for DRONEDARONE, making it a notable side effect.
If you experience oedema peripheral while taking DRONEDARONE, 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.