231 reports of this reaction
4.7% of all LEVONORGESTREL AND ETHINYL ESTRADIOL reports
#1 most reported adverse reaction
NAUSEA is the #1 most commonly reported adverse reaction for LEVONORGESTREL AND ETHINYL ESTRADIOL, manufactured by Teva Pharmaceuticals USA, Inc.. There are 231 FDA adverse event reports linking LEVONORGESTREL AND ETHINYL ESTRADIOL to NAUSEA. This represents approximately 4.7% of all 4,908 adverse event reports for this drug.
Patients taking LEVONORGESTREL AND ETHINYL ESTRADIOL who experience nausea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NAUSEA is moderately reported among LEVONORGESTREL AND ETHINYL ESTRADIOL users, representing a notable but not dominant share of adverse events.
In addition to nausea, the following adverse reactions have been reported for LEVONORGESTREL AND ETHINYL ESTRADIOL:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 231 FDA reports for LEVONORGESTREL AND ETHINYL ESTRADIOL. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 4.7% of all adverse event reports for LEVONORGESTREL AND ETHINYL ESTRADIOL, making it one of the most commonly reported side effect.
If you experience nausea 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.