535 reports of this reaction
3.2% of all ATROPINE reports
#3 most reported adverse reaction
DIARRHOEA is the #3 most commonly reported adverse reaction for ATROPINE, manufactured by Meridian Medical Technologies LLC. There are 535 FDA adverse event reports linking ATROPINE to DIARRHOEA. This represents approximately 3.2% of all 16,519 adverse event reports for this drug.
Patients taking ATROPINE who experience diarrhoea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DIARRHOEA is moderately reported among ATROPINE users, representing a notable but not dominant share of adverse events.
In addition to diarrhoea, the following adverse reactions have been reported for ATROPINE:
The following drugs have also been linked to diarrhoea in FDA adverse event reports:
DIARRHOEA has been reported as an adverse event in 535 FDA reports for ATROPINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIARRHOEA accounts for approximately 3.2% of all adverse event reports for ATROPINE, making it one of the most commonly reported side effect.
If you experience diarrhoea while taking ATROPINE, 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.