5 reports of this reaction
3.4% of all AGNUS CASTUS reports
#7 most reported adverse reaction
ALOPECIA is the #7 most commonly reported adverse reaction for AGNUS CASTUS, manufactured by Boiron. There are 5 FDA adverse event reports linking AGNUS CASTUS to ALOPECIA. This represents approximately 3.4% of all 146 adverse event reports for this drug.
Patients taking AGNUS CASTUS who experience alopecia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ALOPECIA is moderately reported among AGNUS CASTUS users, representing a notable but not dominant share of adverse events.
In addition to alopecia, the following adverse reactions have been reported for AGNUS CASTUS:
The following drugs have also been linked to alopecia in FDA adverse event reports:
ALOPECIA has been reported as an adverse event in 5 FDA reports for AGNUS CASTUS. This does not prove causation, but indicates an association observed in post-market surveillance data.
ALOPECIA accounts for approximately 3.4% of all adverse event reports for AGNUS CASTUS, making it a notable side effect.
If you experience alopecia while taking AGNUS CASTUS, 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.