833 reports of this reaction
1.6% of all ETHYL ALCOHOL reports
#12 most reported adverse reaction
INTENTIONAL PRODUCT MISUSE is the #12 most commonly reported adverse reaction for ETHYL ALCOHOL, manufactured by Walmart Inc.. There are 833 FDA adverse event reports linking ETHYL ALCOHOL to INTENTIONAL PRODUCT MISUSE. This represents approximately 1.6% of all 53,513 adverse event reports for this drug.
Patients taking ETHYL ALCOHOL who experience intentional product misuse should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
INTENTIONAL PRODUCT MISUSE is a less commonly reported adverse event for ETHYL ALCOHOL, but still significant enough to appear in the safety profile.
In addition to intentional product misuse, the following adverse reactions have been reported for ETHYL ALCOHOL:
The following drugs have also been linked to intentional product misuse in FDA adverse event reports:
INTENTIONAL PRODUCT MISUSE has been reported as an adverse event in 833 FDA reports for ETHYL ALCOHOL. This does not prove causation, but indicates an association observed in post-market surveillance data.
INTENTIONAL PRODUCT MISUSE accounts for approximately 1.6% of all adverse event reports for ETHYL ALCOHOL, making it a notable side effect.
If you experience intentional product misuse while taking ETHYL ALCOHOL, 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.