196 reports of this reaction
3.2% of all LEVOCARNITINE reports
#4 most reported adverse reaction
DIARRHOEA is the #4 most commonly reported adverse reaction for LEVOCARNITINE, manufactured by Leadiant Biosciences, Inc.. There are 196 FDA adverse event reports linking LEVOCARNITINE to DIARRHOEA. This represents approximately 3.2% of all 6,090 adverse event reports for this drug.
Patients taking LEVOCARNITINE 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 LEVOCARNITINE users, representing a notable but not dominant share of adverse events.
In addition to diarrhoea, the following adverse reactions have been reported for LEVOCARNITINE:
The following drugs have also been linked to diarrhoea in FDA adverse event reports:
DIARRHOEA has been reported as an adverse event in 196 FDA reports for LEVOCARNITINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIARRHOEA accounts for approximately 3.2% of all adverse event reports for LEVOCARNITINE, making it a notable side effect.
If you experience diarrhoea while taking LEVOCARNITINE, 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.