1 reports of this reaction
3.8% of all BRYONIA ALBA ROOT reports
#12 most reported adverse reaction
HOT FLUSH is the #12 most commonly reported adverse reaction for BRYONIA ALBA ROOT, manufactured by Energique, Inc.. There are 1 FDA adverse event reports linking BRYONIA ALBA ROOT to HOT FLUSH. This represents approximately 3.8% of all 26 adverse event reports for this drug.
Patients taking BRYONIA ALBA ROOT who experience hot flush should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HOT FLUSH is moderately reported among BRYONIA ALBA ROOT users, representing a notable but not dominant share of adverse events.
In addition to hot flush, the following adverse reactions have been reported for BRYONIA ALBA ROOT:
The following drugs have also been linked to hot flush in FDA adverse event reports:
HOT FLUSH has been reported as an adverse event in 1 FDA reports for BRYONIA ALBA ROOT. This does not prove causation, but indicates an association observed in post-market surveillance data.
HOT FLUSH accounts for approximately 3.8% of all adverse event reports for BRYONIA ALBA ROOT, making it a notable side effect.
If you experience hot flush while taking BRYONIA ALBA ROOT, 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.