3,249 reports of this reaction
3.0% of all ETONOGESTREL reports
#10 most reported adverse reaction
COMPLICATION OF DEVICE INSERTION is the #10 most commonly reported adverse reaction for ETONOGESTREL, manufactured by Organon LLC. There are 3,249 FDA adverse event reports linking ETONOGESTREL to COMPLICATION OF DEVICE INSERTION. This represents approximately 3.0% of all 110,074 adverse event reports for this drug.
Patients taking ETONOGESTREL 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 a less commonly reported adverse event for ETONOGESTREL, but still significant enough to appear in the safety profile.
In addition to complication of device insertion, the following adverse reactions have been reported for ETONOGESTREL:
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 3,249 FDA reports for ETONOGESTREL. This does not prove causation, but indicates an association observed in post-market surveillance data.
COMPLICATION OF DEVICE INSERTION accounts for approximately 3.0% of all adverse event reports for ETONOGESTREL, making it a notable side effect.
If you experience complication of device insertion while taking ETONOGESTREL, 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.