1 reports of this reaction
2.4% of all POTASSIUM DICHROMATE reports
#15 most reported adverse reaction
ERECTILE DYSFUNCTION is the #15 most commonly reported adverse reaction for POTASSIUM DICHROMATE, manufactured by BM Private Limited. There are 1 FDA adverse event reports linking POTASSIUM DICHROMATE to ERECTILE DYSFUNCTION. This represents approximately 2.4% of all 41 adverse event reports for this drug.
Patients taking POTASSIUM DICHROMATE who experience erectile dysfunction should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ERECTILE DYSFUNCTION is a less commonly reported adverse event for POTASSIUM DICHROMATE, but still significant enough to appear in the safety profile.
In addition to erectile dysfunction, the following adverse reactions have been reported for POTASSIUM DICHROMATE:
The following drugs have also been linked to erectile dysfunction in FDA adverse event reports:
ERECTILE DYSFUNCTION has been reported as an adverse event in 1 FDA reports for POTASSIUM DICHROMATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
ERECTILE DYSFUNCTION accounts for approximately 2.4% of all adverse event reports for POTASSIUM DICHROMATE, making it a notable side effect.
If you experience erectile dysfunction while taking POTASSIUM DICHROMATE, 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.