1 reports of this reaction
4.2% of all BERBERIS VULGARIS ROOT BARK reports
#16 most reported adverse reaction
MENORRHAGIA is the #16 most commonly reported adverse reaction for BERBERIS VULGARIS ROOT BARK, manufactured by BM Private Limited. There are 1 FDA adverse event reports linking BERBERIS VULGARIS ROOT BARK to MENORRHAGIA. This represents approximately 4.2% of all 24 adverse event reports for this drug.
Patients taking BERBERIS VULGARIS ROOT BARK who experience menorrhagia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
MENORRHAGIA is moderately reported among BERBERIS VULGARIS ROOT BARK users, representing a notable but not dominant share of adverse events.
In addition to menorrhagia, the following adverse reactions have been reported for BERBERIS VULGARIS ROOT BARK:
The following drugs have also been linked to menorrhagia in FDA adverse event reports:
MENORRHAGIA has been reported as an adverse event in 1 FDA reports for BERBERIS VULGARIS ROOT BARK. This does not prove causation, but indicates an association observed in post-market surveillance data.
MENORRHAGIA accounts for approximately 4.2% of all adverse event reports for BERBERIS VULGARIS ROOT BARK, making it a notable side effect.
If you experience menorrhagia while taking BERBERIS VULGARIS ROOT BARK, 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.