29 reports of this reaction
2.7% of all POTASSIUM NITRATE AND SODIUM FLUORIDE reports
#8 most reported adverse reaction
PRODUCT USE IN UNAPPROVED INDICATION is the #8 most commonly reported adverse reaction for POTASSIUM NITRATE AND SODIUM FLUORIDE, manufactured by Haleon US Holdings LLC. There are 29 FDA adverse event reports linking POTASSIUM NITRATE AND SODIUM FLUORIDE to PRODUCT USE IN UNAPPROVED INDICATION. This represents approximately 2.7% of all 1,057 adverse event reports for this drug.
Patients taking POTASSIUM NITRATE AND SODIUM FLUORIDE who experience product use in unapproved indication should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PRODUCT USE IN UNAPPROVED INDICATION is a less commonly reported adverse event for POTASSIUM NITRATE AND SODIUM FLUORIDE, but still significant enough to appear in the safety profile.
In addition to product use in unapproved indication, the following adverse reactions have been reported for POTASSIUM NITRATE AND SODIUM FLUORIDE:
The following drugs have also been linked to product use in unapproved indication in FDA adverse event reports:
PRODUCT USE IN UNAPPROVED INDICATION has been reported as an adverse event in 29 FDA reports for POTASSIUM NITRATE AND SODIUM FLUORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
PRODUCT USE IN UNAPPROVED INDICATION accounts for approximately 2.7% of all adverse event reports for POTASSIUM NITRATE AND SODIUM FLUORIDE, making it a notable side effect.
If you experience product use in unapproved indication 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.