39 reports of this reaction
3.1% of all CANDIDA ALBICANS reports
#1 most reported adverse reaction
DIARRHOEA is the #1 most commonly reported adverse reaction for CANDIDA ALBICANS, manufactured by DNA Labs, Inc.. There are 39 FDA adverse event reports linking CANDIDA ALBICANS to DIARRHOEA. This represents approximately 3.1% of all 1,258 adverse event reports for this drug.
Patients taking CANDIDA ALBICANS who experience diarrhoea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DIARRHOEA is moderately reported among CANDIDA ALBICANS users, representing a notable but not dominant share of adverse events.
In addition to diarrhoea, the following adverse reactions have been reported for CANDIDA ALBICANS:
The following drugs have also been linked to diarrhoea in FDA adverse event reports:
DIARRHOEA has been reported as an adverse event in 39 FDA reports for CANDIDA ALBICANS. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIARRHOEA accounts for approximately 3.1% of all adverse event reports for CANDIDA ALBICANS, making it one of the most commonly reported side effect.
If you experience diarrhoea while taking CANDIDA ALBICANS, 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.