104 reports of this reaction
2.1% of all LEVONORGESTREL AND ETHINYL ESTRADIOL reports
#8 most reported adverse reaction
DIZZINESS is the #8 most commonly reported adverse reaction for LEVONORGESTREL AND ETHINYL ESTRADIOL, manufactured by Teva Pharmaceuticals USA, Inc.. There are 104 FDA adverse event reports linking LEVONORGESTREL AND ETHINYL ESTRADIOL to DIZZINESS. This represents approximately 2.1% of all 4,908 adverse event reports for this drug.
Patients taking LEVONORGESTREL AND ETHINYL 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 LEVONORGESTREL AND ETHINYL ESTRADIOL, but still significant enough to appear in the safety profile.
In addition to dizziness, the following adverse reactions have been reported for LEVONORGESTREL AND ETHINYL ESTRADIOL:
The following drugs have also been linked to dizziness in FDA adverse event reports:
DIZZINESS has been reported as an adverse event in 104 FDA reports for LEVONORGESTREL AND ETHINYL ESTRADIOL. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIZZINESS accounts for approximately 2.1% of all adverse event reports for LEVONORGESTREL AND ETHINYL ESTRADIOL, making it a notable side effect.
If you experience dizziness while taking LEVONORGESTREL AND ETHINYL 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.