2,921 reports of this reaction
1.8% of all ESTRADIOL reports
#10 most reported adverse reaction
DIZZINESS is the #10 most commonly reported adverse reaction for ESTRADIOL, manufactured by Allergan, Inc.. There are 2,921 FDA adverse event reports linking ESTRADIOL to DIZZINESS. This represents approximately 1.8% of all 159,657 adverse event reports for this drug.
Patients taking ESTRADIOL who experience dizziness should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DIZZINESS is a less commonly reported adverse event for ESTRADIOL, but still significant enough to appear in the safety profile.
In addition to dizziness, the following adverse reactions have been reported for ESTRADIOL:
The following drugs have also been linked to dizziness in FDA adverse event reports:
DIZZINESS has been reported as an adverse event in 2,921 FDA reports for ESTRADIOL. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIZZINESS accounts for approximately 1.8% of all adverse event reports for ESTRADIOL, making it a notable side effect.
If you experience dizziness while taking ESTRADIOL, 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.