9,909 reports of this reaction
9.0% of all ETONOGESTREL reports
#1 most reported adverse reaction
NO ADVERSE EVENT is the #1 most commonly reported adverse reaction for ETONOGESTREL, manufactured by Organon LLC. There are 9,909 FDA adverse event reports linking ETONOGESTREL to NO ADVERSE EVENT. This represents approximately 9.0% of all 110,074 adverse event reports for this drug.
Patients taking ETONOGESTREL who experience no adverse event should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NO ADVERSE EVENT is moderately reported among ETONOGESTREL users, representing a notable but not dominant share of adverse events.
In addition to no adverse event, the following adverse reactions have been reported for ETONOGESTREL:
The following drugs have also been linked to no adverse event in FDA adverse event reports:
NO ADVERSE EVENT has been reported as an adverse event in 9,909 FDA reports for ETONOGESTREL. This does not prove causation, but indicates an association observed in post-market surveillance data.
NO ADVERSE EVENT accounts for approximately 9.0% of all adverse event reports for ETONOGESTREL, making it one of the most commonly reported side effect.
If you experience no adverse event 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.