795 reports of this reaction
2.8% of all DRS. CLOTRIMAZOLE reports
#2 most reported adverse reaction
MACULAR DEGENERATION is the #2 most commonly reported adverse reaction for DRS. CLOTRIMAZOLE, manufactured by AARNA USA INC. There are 795 FDA adverse event reports linking DRS. CLOTRIMAZOLE to MACULAR DEGENERATION. This represents approximately 2.8% of all 28,516 adverse event reports for this drug.
Patients taking DRS. CLOTRIMAZOLE who experience macular degeneration should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
MACULAR DEGENERATION is a less commonly reported adverse event for DRS. CLOTRIMAZOLE, but still significant enough to appear in the safety profile.
In addition to macular degeneration, the following adverse reactions have been reported for DRS. CLOTRIMAZOLE:
The following drugs have also been linked to macular degeneration in FDA adverse event reports:
MACULAR DEGENERATION has been reported as an adverse event in 795 FDA reports for DRS. CLOTRIMAZOLE. This does not prove causation, but indicates an association observed in post-market surveillance data.
MACULAR DEGENERATION accounts for approximately 2.8% of all adverse event reports for DRS. CLOTRIMAZOLE, making it one of the most commonly reported side effect.
If you experience macular degeneration while taking DRS. CLOTRIMAZOLE, 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.