900 reports of this reaction
1.6% of all MEDROXYPROGESTERONE ACETATE reports
#9 most reported adverse reaction
DEPRESSION is the #9 most commonly reported adverse reaction for MEDROXYPROGESTERONE ACETATE, manufactured by Pharmacia & Upjohn Company LLC. There are 900 FDA adverse event reports linking MEDROXYPROGESTERONE ACETATE to DEPRESSION. This represents approximately 1.6% of all 57,188 adverse event reports for this drug.
Patients taking MEDROXYPROGESTERONE ACETATE who experience depression should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DEPRESSION is a less commonly reported adverse event for MEDROXYPROGESTERONE ACETATE, but still significant enough to appear in the safety profile.
In addition to depression, the following adverse reactions have been reported for MEDROXYPROGESTERONE ACETATE:
The following drugs have also been linked to depression in FDA adverse event reports:
DEPRESSION has been reported as an adverse event in 900 FDA reports for MEDROXYPROGESTERONE ACETATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DEPRESSION accounts for approximately 1.6% of all adverse event reports for MEDROXYPROGESTERONE ACETATE, making it a notable side effect.
If you experience depression while taking 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.