9,172 reports of this reaction
2.6% of all LEVONORGESTREL reports
#6 most reported adverse reaction
ABDOMINAL PAIN LOWER is the #6 most commonly reported adverse reaction for LEVONORGESTREL, manufactured by Bayer HealthCare Pharmaceuticals Inc.. There are 9,172 FDA adverse event reports linking LEVONORGESTREL to ABDOMINAL PAIN LOWER. This represents approximately 2.6% of all 357,584 adverse event reports for this drug.
Patients taking LEVONORGESTREL who experience abdominal pain lower should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ABDOMINAL PAIN LOWER is a less commonly reported adverse event for LEVONORGESTREL, but still significant enough to appear in the safety profile.
In addition to abdominal pain lower, the following adverse reactions have been reported for LEVONORGESTREL:
The following drugs have also been linked to abdominal pain lower in FDA adverse event reports:
ABDOMINAL PAIN LOWER has been reported as an adverse event in 9,172 FDA reports for LEVONORGESTREL. This does not prove causation, but indicates an association observed in post-market surveillance data.
ABDOMINAL PAIN LOWER accounts for approximately 2.6% of all adverse event reports for LEVONORGESTREL, making it a notable side effect.
If you experience abdominal pain lower while taking LEVONORGESTREL, 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.