8 reports of this reaction
1.6% of all ATROPA BELLADONNA reports
#13 most reported adverse reaction
DECREASED APPETITE is the #13 most commonly reported adverse reaction for ATROPA BELLADONNA. There are 8 FDA adverse event reports linking ATROPA BELLADONNA to DECREASED APPETITE. This represents approximately 1.6% of all 489 adverse event reports for this drug.
Patients taking ATROPA BELLADONNA who experience decreased appetite should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DECREASED APPETITE is a less commonly reported adverse event for ATROPA BELLADONNA, but still significant enough to appear in the safety profile.
In addition to decreased appetite, the following adverse reactions have been reported for ATROPA BELLADONNA:
The following drugs have also been linked to decreased appetite in FDA adverse event reports:
DECREASED APPETITE has been reported as an adverse event in 8 FDA reports for ATROPA BELLADONNA. This does not prove causation, but indicates an association observed in post-market surveillance data.
DECREASED APPETITE accounts for approximately 1.6% of all adverse event reports for ATROPA BELLADONNA, making it a notable side effect.
If you experience decreased appetite while taking ATROPA BELLADONNA, 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.