3,806 reports of this reaction
2.0% of all PAROXETINE HYDROCHLORIDE reports
#9 most reported adverse reaction
DIARRHOEA is the #9 most commonly reported adverse reaction for PAROXETINE HYDROCHLORIDE, manufactured by Apotex Corp. There are 3,806 FDA adverse event reports linking PAROXETINE HYDROCHLORIDE to DIARRHOEA. This represents approximately 2.0% of all 192,057 adverse event reports for this drug.
PAROXETINE HYDROCHLORIDE has an overall safety score of 78 out of 100. Patients taking PAROXETINE HYDROCHLORIDE 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 a less commonly reported adverse event for PAROXETINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to diarrhoea, the following adverse reactions have been reported for PAROXETINE HYDROCHLORIDE:
The following drugs have also been linked to diarrhoea in FDA adverse event reports:
DIARRHOEA has been reported as an adverse event in 3,806 FDA reports for PAROXETINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIARRHOEA accounts for approximately 2.0% of all adverse event reports for PAROXETINE HYDROCHLORIDE, making it a notable side effect.
If you experience diarrhoea while taking PAROXETINE HYDROCHLORIDE, 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.