4 reports of this reaction
4.0% of all DEXTROSE(GLUCOSE),LEVULOSE(FRUCTOSE),PHOSPHORIC ACID reports
#3 most reported adverse reaction
DRY MOUTH is the #3 most commonly reported adverse reaction for DEXTROSE(GLUCOSE),LEVULOSE(FRUCTOSE),PHOSPHORIC ACID, manufactured by Cardinal Health. There are 4 FDA adverse event reports linking DEXTROSE(GLUCOSE),LEVULOSE(FRUCTOSE),PHOSPHORIC ACID to DRY MOUTH. This represents approximately 4.0% of all 101 adverse event reports for this drug.
Patients taking DEXTROSE(GLUCOSE),LEVULOSE(FRUCTOSE),PHOSPHORIC ACID who experience dry mouth should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DRY MOUTH is moderately reported among DEXTROSE(GLUCOSE),LEVULOSE(FRUCTOSE),PHOSPHORIC ACID users, representing a notable but not dominant share of adverse events.
In addition to dry mouth, the following adverse reactions have been reported for DEXTROSE(GLUCOSE),LEVULOSE(FRUCTOSE),PHOSPHORIC ACID:
The following drugs have also been linked to dry mouth in FDA adverse event reports:
DRY MOUTH has been reported as an adverse event in 4 FDA reports for DEXTROSE(GLUCOSE),LEVULOSE(FRUCTOSE),PHOSPHORIC ACID. This does not prove causation, but indicates an association observed in post-market surveillance data.
DRY MOUTH accounts for approximately 4.0% of all adverse event reports for DEXTROSE(GLUCOSE),LEVULOSE(FRUCTOSE),PHOSPHORIC ACID, making it one of the most commonly reported side effect.
If you experience dry mouth while taking DEXTROSE(GLUCOSE),LEVULOSE(FRUCTOSE),PHOSPHORIC ACID, 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.