3,764 reports of this reaction
3.2% of all COPPER reports
#8 most reported adverse reaction
REPRODUCTIVE COMPLICATION ASSOCIATED WITH DEVICE is the #8 most commonly reported adverse reaction for COPPER, manufactured by CooperSurgical, Inc.. There are 3,764 FDA adverse event reports linking COPPER to REPRODUCTIVE COMPLICATION ASSOCIATED WITH DEVICE. This represents approximately 3.2% of all 116,047 adverse event reports for this drug.
Patients taking COPPER who experience reproductive complication associated with device should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
REPRODUCTIVE COMPLICATION ASSOCIATED WITH DEVICE is moderately reported among COPPER users, representing a notable but not dominant share of adverse events.
In addition to reproductive complication associated with device, the following adverse reactions have been reported for COPPER:
REPRODUCTIVE COMPLICATION ASSOCIATED WITH DEVICE has been reported as an adverse event in 3,764 FDA reports for COPPER. This does not prove causation, but indicates an association observed in post-market surveillance data.
REPRODUCTIVE COMPLICATION ASSOCIATED WITH DEVICE accounts for approximately 3.2% of all adverse event reports for COPPER, making it a notable side effect.
If you experience reproductive complication associated with device 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.