56 reports of this reaction
5.2% of all POTASSIUM NITRATE, SODIUM FLUORIDE reports
#4 most reported adverse reaction
HYPERAESTHESIA TEETH is the #4 most commonly reported adverse reaction for POTASSIUM NITRATE, SODIUM FLUORIDE, manufactured by Haleon US Holdings LLC. There are 56 FDA adverse event reports linking POTASSIUM NITRATE, SODIUM FLUORIDE to HYPERAESTHESIA TEETH. This represents approximately 5.2% of all 1,087 adverse event reports for this drug.
Patients taking POTASSIUM NITRATE, SODIUM FLUORIDE who experience hyperaesthesia teeth should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HYPERAESTHESIA TEETH is moderately reported among POTASSIUM NITRATE, SODIUM FLUORIDE users, representing a notable but not dominant share of adverse events.
In addition to hyperaesthesia teeth, the following adverse reactions have been reported for POTASSIUM NITRATE, SODIUM FLUORIDE:
The following drugs have also been linked to hyperaesthesia teeth in FDA adverse event reports:
HYPERAESTHESIA TEETH has been reported as an adverse event in 56 FDA reports for POTASSIUM NITRATE, SODIUM FLUORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
HYPERAESTHESIA TEETH accounts for approximately 5.2% of all adverse event reports for POTASSIUM NITRATE, SODIUM FLUORIDE, making it a notable side effect.
If you experience hyperaesthesia teeth 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.