18 reports of this reaction
2.3% of all BARIUM SULFATE reports
#6 most reported adverse reaction
DYSPNOEA is the #6 most commonly reported adverse reaction for BARIUM SULFATE, manufactured by E-Z-EM Canada Inc. There are 18 FDA adverse event reports linking BARIUM SULFATE to DYSPNOEA. This represents approximately 2.3% of all 781 adverse event reports for this drug.
Patients taking BARIUM SULFATE 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 BARIUM SULFATE, but still significant enough to appear in the safety profile.
In addition to dyspnoea, the following adverse reactions have been reported for BARIUM SULFATE:
The following drugs have also been linked to dyspnoea in FDA adverse event reports:
DYSPNOEA has been reported as an adverse event in 18 FDA reports for BARIUM SULFATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DYSPNOEA accounts for approximately 2.3% of all adverse event reports for BARIUM SULFATE, making it a notable side effect.
If you experience dyspnoea while taking BARIUM SULFATE, 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.