1 reports of this reaction
6.3% of all MICONAZOLE NITRATE 2% reports
#6 most reported adverse reaction
DISEASE PROGRESSION is the #6 most commonly reported adverse reaction for MICONAZOLE NITRATE 2%, manufactured by Akron Pharma Inc.. There are 1 FDA adverse event reports linking MICONAZOLE NITRATE 2% to DISEASE PROGRESSION. This represents approximately 6.3% of all 16 adverse event reports for this drug.
Patients taking MICONAZOLE NITRATE 2% who experience disease progression should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DISEASE PROGRESSION is moderately reported among MICONAZOLE NITRATE 2% users, representing a notable but not dominant share of adverse events.
In addition to disease progression, the following adverse reactions have been reported for MICONAZOLE NITRATE 2%:
The following drugs have also been linked to disease progression in FDA adverse event reports:
DISEASE PROGRESSION has been reported as an adverse event in 1 FDA reports for MICONAZOLE NITRATE 2%. This does not prove causation, but indicates an association observed in post-market surveillance data.
DISEASE PROGRESSION accounts for approximately 6.3% of all adverse event reports for MICONAZOLE NITRATE 2%, making it a notable side effect.
If you experience disease progression while taking MICONAZOLE NITRATE 2%, 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.