6,075 reports of this reaction
5.2% of all COPPER reports
#6 most reported adverse reaction
COMPLICATION OF DEVICE INSERTION is the #6 most commonly reported adverse reaction for COPPER, manufactured by CooperSurgical, Inc.. There are 6,075 FDA adverse event reports linking COPPER to COMPLICATION OF DEVICE INSERTION. This represents approximately 5.2% of all 116,047 adverse event reports for this drug.
Patients taking COPPER who experience complication of device insertion should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
COMPLICATION OF DEVICE INSERTION is moderately reported among COPPER users, representing a notable but not dominant share of adverse events.
In addition to complication of device insertion, the following adverse reactions have been reported for COPPER:
The following drugs have also been linked to complication of device insertion in FDA adverse event reports:
COMPLICATION OF DEVICE INSERTION has been reported as an adverse event in 6,075 FDA reports for COPPER. This does not prove causation, but indicates an association observed in post-market surveillance data.
COMPLICATION OF DEVICE INSERTION accounts for approximately 5.2% of all adverse event reports for COPPER, making it a notable side effect.
If you experience complication of device insertion 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.