COPPER and EMBEDDED DEVICE

Overview

EMBEDDED DEVICE is the #9 most commonly reported adverse reaction for COPPER, manufactured by CooperSurgical, Inc.. There are 3,603 FDA adverse event reports linking COPPER to EMBEDDED DEVICE. This represents approximately 3.1% of all 116,047 adverse event reports for this drug.

Patients taking COPPER who experience embedded 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.

Reporting Frequency

EMBEDDED DEVICE is moderately reported among COPPER users, representing a notable but not dominant share of adverse events.

Other Side Effects of COPPER

In addition to embedded device, the following adverse reactions have been reported for COPPER:

• DEVICE EXPULSION — 10,636 reports
• DEVICE BREAKAGE — 9,388 reports
• COMPLICATION OF DEVICE REMOVAL — 8,216 reports
• FOREIGN BODY IN REPRODUCTIVE TRACT — 7,285 reports
• DEVICE DISLOCATION — 6,762 reports
• COMPLICATION OF DEVICE INSERTION — 6,075 reports
• PAIN — 5,274 reports
• REPRODUCTIVE COMPLICATION ASSOCIATED WITH DEVICE — 3,764 reports
• INJURY ASSOCIATED WITH DEVICE — 2,852 reports
• ANXIETY — 2,580 reports

Does COPPER cause EMBEDDED DEVICE?

EMBEDDED DEVICE has been reported as an adverse event in 3,603 FDA reports for COPPER. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is EMBEDDED DEVICE with COPPER?

EMBEDDED DEVICE accounts for approximately 3.1% of all adverse event reports for COPPER, making it a notable side effect.

What should I do if I experience EMBEDDED DEVICE while taking COPPER?

If you experience embedded 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.

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