568 reports of this reaction
3.6% of all CHLORPHENIRAMINE MALEATE reports
#2 most reported adverse reaction
DIARRHOEA is the #2 most commonly reported adverse reaction for CHLORPHENIRAMINE MALEATE, manufactured by Rite Aid Corporation. There are 568 FDA adverse event reports linking CHLORPHENIRAMINE MALEATE to DIARRHOEA. This represents approximately 3.6% of all 15,638 adverse event reports for this drug.
Patients taking CHLORPHENIRAMINE MALEATE 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 CHLORPHENIRAMINE MALEATE users, representing a notable but not dominant share of adverse events.
In addition to diarrhoea, the following adverse reactions have been reported for CHLORPHENIRAMINE MALEATE:
The following drugs have also been linked to diarrhoea in FDA adverse event reports:
DIARRHOEA has been reported as an adverse event in 568 FDA reports for CHLORPHENIRAMINE MALEATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIARRHOEA accounts for approximately 3.6% of all adverse event reports for CHLORPHENIRAMINE MALEATE, making it one of the most commonly reported side effect.
If you experience diarrhoea while taking CHLORPHENIRAMINE MALEATE, 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.