5 reports of this reaction
3.4% of all AGNUS CASTUS reports
#6 most reported adverse reaction
ACNE CYSTIC is the #6 most commonly reported adverse reaction for AGNUS CASTUS, manufactured by Boiron. There are 5 FDA adverse event reports linking AGNUS CASTUS to ACNE CYSTIC. This represents approximately 3.4% of all 146 adverse event reports for this drug.
Patients taking AGNUS CASTUS who experience acne cystic should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ACNE CYSTIC is moderately reported among AGNUS CASTUS users, representing a notable but not dominant share of adverse events.
In addition to acne cystic, the following adverse reactions have been reported for AGNUS CASTUS:
ACNE CYSTIC 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.
ACNE CYSTIC accounts for approximately 3.4% of all adverse event reports for AGNUS CASTUS, making it a notable side effect.
If you experience acne cystic 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.