1 reports of this reaction
8.3% of all HAND SANITIZER reports
#6 most reported adverse reaction
PRODUCT ODOUR ABNORMAL is the #6 most commonly reported adverse reaction for HAND SANITIZER, manufactured by Raining Rose, Inc. There are 1 FDA adverse event reports linking HAND SANITIZER to PRODUCT ODOUR ABNORMAL. This represents approximately 8.3% of all 12 adverse event reports for this drug.
Patients taking HAND SANITIZER who experience product odour abnormal 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 ODOUR ABNORMAL is moderately reported among HAND SANITIZER users, representing a notable but not dominant share of adverse events.
In addition to product odour abnormal, the following adverse reactions have been reported for HAND SANITIZER:
The following drugs have also been linked to product odour abnormal in FDA adverse event reports:
PRODUCT ODOUR ABNORMAL 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.
PRODUCT ODOUR ABNORMAL accounts for approximately 8.3% of all adverse event reports for HAND SANITIZER, making it a notable side effect.
If you experience product odour abnormal 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.