711 reports of this reaction
4.1% of all BISMUTH SUBSALICYLATE reports
#4 most reported adverse reaction
DIARRHOEA is the #4 most commonly reported adverse reaction for BISMUTH SUBSALICYLATE, manufactured by Lil' Drug Store Products, Inc.. There are 711 FDA adverse event reports linking BISMUTH SUBSALICYLATE to DIARRHOEA. This represents approximately 4.1% of all 17,164 adverse event reports for this drug.
Patients taking BISMUTH SUBSALICYLATE 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 BISMUTH SUBSALICYLATE users, representing a notable but not dominant share of adverse events.
In addition to diarrhoea, the following adverse reactions have been reported for BISMUTH SUBSALICYLATE:
The following drugs have also been linked to diarrhoea in FDA adverse event reports:
DIARRHOEA has been reported as an adverse event in 711 FDA reports for BISMUTH SUBSALICYLATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIARRHOEA accounts for approximately 4.1% of all adverse event reports for BISMUTH SUBSALICYLATE, making it a notable side effect.
If you experience diarrhoea while taking BISMUTH SUBSALICYLATE, 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.