1 reports of this reaction
8.3% of all HAND SANITIZER reports
#2 most reported adverse reaction
APPLICATION SITE DRYNESS is the #2 most commonly reported adverse reaction for HAND SANITIZER, manufactured by Raining Rose, Inc. There are 1 FDA adverse event reports linking HAND SANITIZER to APPLICATION SITE DRYNESS. This represents approximately 8.3% of all 12 adverse event reports for this drug.
Patients taking HAND SANITIZER who experience application site dryness should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
APPLICATION SITE DRYNESS is moderately reported among HAND SANITIZER users, representing a notable but not dominant share of adverse events.
In addition to application site dryness, the following adverse reactions have been reported for HAND SANITIZER:
The following drugs have also been linked to application site dryness in FDA adverse event reports:
APPLICATION SITE DRYNESS has been reported as an adverse event in 1 FDA reports for HAND SANITIZER. This does not prove causation, but indicates an association observed in post-market surveillance data.
APPLICATION SITE DRYNESS accounts for approximately 8.3% of all adverse event reports for HAND SANITIZER, making it one of the most commonly reported side effect.
If you experience application site dryness while taking HAND SANITIZER, 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.