4,562 reports of this reaction
4.1% of all ETONOGESTREL reports
#4 most reported adverse reaction
DEVICE DIFFICULT TO USE is the #4 most commonly reported adverse reaction for ETONOGESTREL, manufactured by Organon LLC. There are 4,562 FDA adverse event reports linking ETONOGESTREL to DEVICE DIFFICULT TO USE. This represents approximately 4.1% of all 110,074 adverse event reports for this drug.
Patients taking ETONOGESTREL who experience device difficult to use should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DEVICE DIFFICULT TO USE is moderately reported among ETONOGESTREL users, representing a notable but not dominant share of adverse events.
In addition to device difficult to use, the following adverse reactions have been reported for ETONOGESTREL:
The following drugs have also been linked to device difficult to use in FDA adverse event reports:
DEVICE DIFFICULT TO USE has been reported as an adverse event in 4,562 FDA reports for ETONOGESTREL. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEVICE DIFFICULT TO USE accounts for approximately 4.1% of all adverse event reports for ETONOGESTREL, making it a notable side effect.
If you experience device difficult to use 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.