6 reports of this reaction
4.1% of all AGNUS CASTUS reports
#1 most reported adverse reaction
ABDOMINAL DISTENSION is the #1 most commonly reported adverse reaction for AGNUS CASTUS, manufactured by Boiron. There are 6 FDA adverse event reports linking AGNUS CASTUS to ABDOMINAL DISTENSION. This represents approximately 4.1% of all 146 adverse event reports for this drug.
Patients taking AGNUS CASTUS who experience abdominal distension should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ABDOMINAL DISTENSION is moderately reported among AGNUS CASTUS users, representing a notable but not dominant share of adverse events.
In addition to abdominal distension, the following adverse reactions have been reported for AGNUS CASTUS:
The following drugs have also been linked to abdominal distension in FDA adverse event reports:
ABDOMINAL DISTENSION has been reported as an adverse event in 6 FDA reports for AGNUS CASTUS. This does not prove causation, but indicates an association observed in post-market surveillance data.
ABDOMINAL DISTENSION accounts for approximately 4.1% of all adverse event reports for AGNUS CASTUS, making it one of the most commonly reported side effect.
If you experience abdominal distension 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.