101 reports of this reaction
6.4% of all STANNOUS FLUORIDE reports
#1 most reported adverse reaction
ORAL DISCOMFORT is the #1 most commonly reported adverse reaction for STANNOUS FLUORIDE, manufactured by Haleon US Holdings LLC. There are 101 FDA adverse event reports linking STANNOUS FLUORIDE to ORAL DISCOMFORT. This represents approximately 6.4% of all 1,587 adverse event reports for this drug.
Patients taking STANNOUS 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 STANNOUS 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 STANNOUS 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 101 FDA reports for STANNOUS FLUORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ORAL DISCOMFORT accounts for approximately 6.4% of all adverse event reports for STANNOUS FLUORIDE, making it one of the most commonly reported side effect.
If you experience oral discomfort while taking STANNOUS 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.