10,636 reports of this reaction
9.2% of all COPPER reports
#1 most reported adverse reaction
DEVICE EXPULSION is the #1 most commonly reported adverse reaction for COPPER, manufactured by CooperSurgical, Inc.. There are 10,636 FDA adverse event reports linking COPPER to DEVICE EXPULSION. This represents approximately 9.2% of all 116,047 adverse event reports for this drug.
Patients taking COPPER who experience device expulsion should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DEVICE EXPULSION is moderately reported among COPPER users, representing a notable but not dominant share of adverse events.
In addition to device expulsion, the following adverse reactions have been reported for COPPER:
The following drugs have also been linked to device expulsion in FDA adverse event reports:
DEVICE EXPULSION has been reported as an adverse event in 10,636 FDA reports for COPPER. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEVICE EXPULSION accounts for approximately 9.2% of all adverse event reports for COPPER, making it one of the most commonly reported side effect.
If you experience device expulsion while taking COPPER, 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.