270 reports of this reaction
2.4% of all POTASSIUM IODIDE reports
#1 most reported adverse reaction
DIARRHOEA is the #1 most commonly reported adverse reaction for POTASSIUM IODIDE, manufactured by Avondale Pharmaceuticals, LLC. There are 270 FDA adverse event reports linking POTASSIUM IODIDE to DIARRHOEA. This represents approximately 2.4% of all 11,184 adverse event reports for this drug.
Patients taking POTASSIUM IODIDE 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 a less commonly reported adverse event for POTASSIUM IODIDE, but still significant enough to appear in the safety profile.
In addition to diarrhoea, the following adverse reactions have been reported for POTASSIUM IODIDE:
The following drugs have also been linked to diarrhoea in FDA adverse event reports:
DIARRHOEA has been reported as an adverse event in 270 FDA reports for POTASSIUM IODIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIARRHOEA accounts for approximately 2.4% of all adverse event reports for POTASSIUM IODIDE, making it one of the most commonly reported side effect.
If you experience diarrhoea while taking POTASSIUM IODIDE, 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.