1,108 reports of this reaction
1.4% of all ESTRADIOL GEL 0.1% reports
#19 most reported adverse reaction
HOT FLUSH is the #19 most commonly reported adverse reaction for ESTRADIOL GEL 0.1%, manufactured by ANI Pharmaceuticals, Inc.. There are 1,108 FDA adverse event reports linking ESTRADIOL GEL 0.1% to HOT FLUSH. This represents approximately 1.4% of all 79,046 adverse event reports for this drug.
Patients taking ESTRADIOL GEL 0.1% who experience hot flush should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HOT FLUSH is a less commonly reported adverse event for ESTRADIOL GEL 0.1%, but still significant enough to appear in the safety profile.
In addition to hot flush, the following adverse reactions have been reported for ESTRADIOL GEL 0.1%:
The following drugs have also been linked to hot flush in FDA adverse event reports:
HOT FLUSH has been reported as an adverse event in 1,108 FDA reports for ESTRADIOL GEL 0.1%. This does not prove causation, but indicates an association observed in post-market surveillance data.
HOT FLUSH accounts for approximately 1.4% of all adverse event reports for ESTRADIOL GEL 0.1%, making it a notable side effect.
If you experience hot flush while taking ESTRADIOL GEL 0.1%, 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.