171 reports of this reaction
1.2% of all MICONAZOLE NITRATE reports
#18 most reported adverse reaction
BURNING SENSATION is the #18 most commonly reported adverse reaction for MICONAZOLE NITRATE, manufactured by H E B. There are 171 FDA adverse event reports linking MICONAZOLE NITRATE to BURNING SENSATION. This represents approximately 1.2% of all 14,417 adverse event reports for this drug.
Patients taking MICONAZOLE NITRATE who experience burning sensation should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
BURNING SENSATION is a less commonly reported adverse event for MICONAZOLE NITRATE, but still significant enough to appear in the safety profile.
In addition to burning sensation, the following adverse reactions have been reported for MICONAZOLE NITRATE:
The following drugs have also been linked to burning sensation in FDA adverse event reports:
BURNING SENSATION has been reported as an adverse event in 171 FDA reports for MICONAZOLE NITRATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
BURNING SENSATION accounts for approximately 1.2% of all adverse event reports for MICONAZOLE NITRATE, making it a notable side effect.
If you experience burning sensation while taking MICONAZOLE NITRATE, 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.