6 reports of this reaction
3.0% of all PAIN RELIEF reports
#2 most reported adverse reaction
DYSPNOEA is the #2 most commonly reported adverse reaction for PAIN RELIEF, manufactured by H E B. There are 6 FDA adverse event reports linking PAIN RELIEF to DYSPNOEA. This represents approximately 3.0% of all 202 adverse event reports for this drug.
Patients taking PAIN RELIEF who experience dyspnoea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DYSPNOEA is a less commonly reported adverse event for PAIN RELIEF, but still significant enough to appear in the safety profile.
In addition to dyspnoea, the following adverse reactions have been reported for PAIN RELIEF:
The following drugs have also been linked to dyspnoea in FDA adverse event reports:
DYSPNOEA has been reported as an adverse event in 6 FDA reports for PAIN RELIEF. This does not prove causation, but indicates an association observed in post-market surveillance data.
DYSPNOEA accounts for approximately 3.0% of all adverse event reports for PAIN RELIEF, making it one of the most commonly reported side effect.
If you experience dyspnoea 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.