3 reports of this reaction
1.5% of all PAIN RELIEF reports
#15 most reported adverse reaction
HAEMORRHOIDS is the #15 most commonly reported adverse reaction for PAIN RELIEF, manufactured by H E B. There are 3 FDA adverse event reports linking PAIN RELIEF to HAEMORRHOIDS. This represents approximately 1.5% of all 202 adverse event reports for this drug.
Patients taking PAIN RELIEF who experience haemorrhoids should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
HAEMORRHOIDS is a less commonly reported adverse event for PAIN RELIEF, but still significant enough to appear in the safety profile.
In addition to haemorrhoids, the following adverse reactions have been reported for PAIN RELIEF:
The following drugs have also been linked to haemorrhoids in FDA adverse event reports:
HAEMORRHOIDS has been reported as an adverse event in 3 FDA reports for PAIN RELIEF. This does not prove causation, but indicates an association observed in post-market surveillance data.
HAEMORRHOIDS accounts for approximately 1.5% of all adverse event reports for PAIN RELIEF, making it a notable side effect.
If you experience haemorrhoids while taking PAIN RELIEF, 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.