277 reports of this reaction
2.4% of all NORETHINDRONE reports
#8 most reported adverse reaction
VAGINAL HAEMORRHAGE is the #8 most commonly reported adverse reaction for NORETHINDRONE, manufactured by Amneal Pharmaceuticals LLC. There are 277 FDA adverse event reports linking NORETHINDRONE to VAGINAL HAEMORRHAGE. This represents approximately 2.4% of all 11,560 adverse event reports for this drug.
Patients taking NORETHINDRONE who experience vaginal haemorrhage should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
VAGINAL HAEMORRHAGE is a less commonly reported adverse event for NORETHINDRONE, but still significant enough to appear in the safety profile.
In addition to vaginal haemorrhage, the following adverse reactions have been reported for NORETHINDRONE:
The following drugs have also been linked to vaginal haemorrhage in FDA adverse event reports:
VAGINAL HAEMORRHAGE has been reported as an adverse event in 277 FDA reports for NORETHINDRONE. This does not prove causation, but indicates an association observed in post-market surveillance data.
VAGINAL HAEMORRHAGE accounts for approximately 2.4% of all adverse event reports for NORETHINDRONE, making it a notable side effect.
If you experience vaginal haemorrhage while taking NORETHINDRONE, 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.