8,511 reports of this reaction
13.0% of all MINOXIDIL reports
#1 most reported adverse reaction
ADVERSE DRUG REACTION is the #1 most commonly reported adverse reaction for MINOXIDIL, manufactured by Kenvue Brands LLC. There are 8,511 FDA adverse event reports linking MINOXIDIL to ADVERSE DRUG REACTION. This represents approximately 13.0% of all 65,386 adverse event reports for this drug.
MINOXIDIL has an overall safety score of 78 out of 100. Patients taking MINOXIDIL who experience adverse drug reaction should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ADVERSE DRUG REACTION is a frequently reported adverse event for MINOXIDIL, accounting for a significant proportion of all reports.
In addition to adverse drug reaction, the following adverse reactions have been reported for MINOXIDIL:
The following drugs have also been linked to adverse drug reaction in FDA adverse event reports:
ADVERSE DRUG REACTION has been reported as an adverse event in 8,511 FDA reports for MINOXIDIL. This does not prove causation, but indicates an association observed in post-market surveillance data.
ADVERSE DRUG REACTION accounts for approximately 13.0% of all adverse event reports for MINOXIDIL, making it one of the most commonly reported side effect.
If you experience adverse drug reaction while taking MINOXIDIL, 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.