2 reports of this reaction
3.8% of all APIS MELLIFERA reports
#2 most reported adverse reaction
ABDOMINAL DISTENSION is the #2 most commonly reported adverse reaction for APIS MELLIFERA, manufactured by Boiron. There are 2 FDA adverse event reports linking APIS MELLIFERA to ABDOMINAL DISTENSION. This represents approximately 3.8% of all 52 adverse event reports for this drug.
Patients taking APIS MELLIFERA 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 APIS MELLIFERA users, representing a notable but not dominant share of adverse events.
In addition to abdominal distension, the following adverse reactions have been reported for APIS MELLIFERA:
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 2 FDA reports for APIS MELLIFERA. This does not prove causation, but indicates an association observed in post-market surveillance data.
ABDOMINAL DISTENSION accounts for approximately 3.8% of all adverse event reports for APIS MELLIFERA, making it one of the most commonly reported side effect.
If you experience abdominal distension while taking APIS MELLIFERA, 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.