408 reports of this reaction
1.2% of all CONJUGATED ESTROGENS AND MEDROXYPROGESTERONE ACETATE reports
#9 most reported adverse reaction
NAUSEA is the #9 most commonly reported adverse reaction for CONJUGATED ESTROGENS AND MEDROXYPROGESTERONE ACETATE, manufactured by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.. There are 408 FDA adverse event reports linking CONJUGATED ESTROGENS AND MEDROXYPROGESTERONE ACETATE to NAUSEA. This represents approximately 1.2% of all 33,191 adverse event reports for this drug.
Patients taking CONJUGATED ESTROGENS AND MEDROXYPROGESTERONE ACETATE 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 a less commonly reported adverse event for CONJUGATED ESTROGENS AND MEDROXYPROGESTERONE ACETATE, but still significant enough to appear in the safety profile.
In addition to nausea, the following adverse reactions have been reported for CONJUGATED ESTROGENS AND MEDROXYPROGESTERONE ACETATE:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 408 FDA reports for CONJUGATED ESTROGENS AND MEDROXYPROGESTERONE ACETATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 1.2% of all adverse event reports for CONJUGATED ESTROGENS AND MEDROXYPROGESTERONE ACETATE, making it a notable side effect.
If you experience nausea while taking CONJUGATED ESTROGENS AND MEDROXYPROGESTERONE ACETATE, 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.