16 reports of this reaction
1.5% of all POTASSIUM NITRATE, SODIUM FLUORIDE reports
#13 most reported adverse reaction
STOMATITIS is the #13 most commonly reported adverse reaction for POTASSIUM NITRATE, SODIUM FLUORIDE, manufactured by Haleon US Holdings LLC. There are 16 FDA adverse event reports linking POTASSIUM NITRATE, SODIUM FLUORIDE to STOMATITIS. This represents approximately 1.5% of all 1,087 adverse event reports for this drug.
Patients taking POTASSIUM NITRATE, SODIUM FLUORIDE who experience stomatitis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
STOMATITIS is a less commonly reported adverse event for POTASSIUM NITRATE, SODIUM FLUORIDE, but still significant enough to appear in the safety profile.
In addition to stomatitis, the following adverse reactions have been reported for POTASSIUM NITRATE, SODIUM FLUORIDE:
The following drugs have also been linked to stomatitis in FDA adverse event reports:
STOMATITIS has been reported as an adverse event in 16 FDA reports for POTASSIUM NITRATE, SODIUM FLUORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
STOMATITIS accounts for approximately 1.5% of all adverse event reports for POTASSIUM NITRATE, SODIUM FLUORIDE, making it a notable side effect.
If you experience stomatitis while taking POTASSIUM NITRATE, SODIUM FLUORIDE, 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.