5,228 reports of this reaction
4.7% of all ETONOGESTREL reports
#3 most reported adverse reaction
COMPLICATION ASSOCIATED WITH DEVICE is the #3 most commonly reported adverse reaction for ETONOGESTREL, manufactured by Organon LLC. There are 5,228 FDA adverse event reports linking ETONOGESTREL to COMPLICATION ASSOCIATED WITH DEVICE. This represents approximately 4.7% of all 110,074 adverse event reports for this drug.
Patients taking ETONOGESTREL who experience 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.
COMPLICATION ASSOCIATED WITH DEVICE is moderately reported among ETONOGESTREL users, representing a notable but not dominant share of adverse events.
In addition to complication associated with device, the following adverse reactions have been reported for ETONOGESTREL:
COMPLICATION ASSOCIATED WITH DEVICE has been reported as an adverse event in 5,228 FDA reports for ETONOGESTREL. This does not prove causation, but indicates an association observed in post-market surveillance data.
COMPLICATION ASSOCIATED WITH DEVICE accounts for approximately 4.7% of all adverse event reports for ETONOGESTREL, making it one of the most commonly reported side effect.
If you experience complication associated with device 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.