472 reports of this reaction
1.7% of all FAMILY WELLNESS CLOTRIMAZOLE reports
#11 most reported adverse reaction
MALAISE is the #11 most commonly reported adverse reaction for FAMILY WELLNESS CLOTRIMAZOLE, manufactured by AARNA USA INC. There are 472 FDA adverse event reports linking FAMILY WELLNESS CLOTRIMAZOLE to MALAISE. This represents approximately 1.7% of all 28,516 adverse event reports for this drug.
Patients taking FAMILY WELLNESS CLOTRIMAZOLE who experience malaise should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
MALAISE is a less commonly reported adverse event for FAMILY WELLNESS CLOTRIMAZOLE, but still significant enough to appear in the safety profile.
In addition to malaise, the following adverse reactions have been reported for FAMILY WELLNESS CLOTRIMAZOLE:
The following drugs have also been linked to malaise in FDA adverse event reports:
MALAISE has been reported as an adverse event in 472 FDA reports for FAMILY WELLNESS CLOTRIMAZOLE. This does not prove causation, but indicates an association observed in post-market surveillance data.
MALAISE accounts for approximately 1.7% of all adverse event reports for FAMILY WELLNESS CLOTRIMAZOLE, making it a notable side effect.
If you experience malaise while taking FAMILY WELLNESS 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.