79 reports of this reaction
7.5% of all POTASSIUM NITRATE AND SODIUM FLUORIDE reports
#1 most reported adverse reaction
ORAL DISCOMFORT is the #1 most commonly reported adverse reaction for POTASSIUM NITRATE AND SODIUM FLUORIDE, manufactured by Haleon US Holdings LLC. There are 79 FDA adverse event reports linking POTASSIUM NITRATE AND SODIUM FLUORIDE to ORAL DISCOMFORT. This represents approximately 7.5% of all 1,057 adverse event reports for this drug.
Patients taking POTASSIUM NITRATE AND SODIUM FLUORIDE who experience oral discomfort should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ORAL DISCOMFORT is moderately reported among POTASSIUM NITRATE AND SODIUM FLUORIDE users, representing a notable but not dominant share of adverse events.
In addition to oral discomfort, the following adverse reactions have been reported for POTASSIUM NITRATE AND SODIUM FLUORIDE:
The following drugs have also been linked to oral discomfort in FDA adverse event reports:
ORAL DISCOMFORT has been reported as an adverse event in 79 FDA reports for POTASSIUM NITRATE AND SODIUM FLUORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ORAL DISCOMFORT accounts for approximately 7.5% of all adverse event reports for POTASSIUM NITRATE AND SODIUM FLUORIDE, making it one of the most commonly reported side effect.
If you experience oral discomfort while taking POTASSIUM NITRATE AND 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.