16 reports of this reaction
3.7% of all POTASSIUM NITRATE reports
#3 most reported adverse reaction
HYPERAESTHESIA TEETH is the #3 most commonly reported adverse reaction for POTASSIUM NITRATE. There are 16 FDA adverse event reports linking POTASSIUM NITRATE to HYPERAESTHESIA TEETH. This represents approximately 3.7% of all 437 adverse event reports for this drug.
Patients taking POTASSIUM NITRATE 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 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:
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 16 FDA reports for POTASSIUM NITRATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
HYPERAESTHESIA TEETH accounts for approximately 3.7% of all adverse event reports for POTASSIUM NITRATE, making it one of the most commonly reported side effect.
If you experience hyperaesthesia teeth while taking POTASSIUM NITRATE, 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.