3 reports of this reaction
2.3% of all PURIFIED WATER reports
#6 most reported adverse reaction
OESOPHAGITIS is the #6 most commonly reported adverse reaction for PURIFIED WATER, manufactured by McKesson. There are 3 FDA adverse event reports linking PURIFIED WATER to OESOPHAGITIS. This represents approximately 2.3% of all 130 adverse event reports for this drug.
Patients taking PURIFIED WATER who experience oesophagitis should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
OESOPHAGITIS is a less commonly reported adverse event for PURIFIED WATER, but still significant enough to appear in the safety profile.
In addition to oesophagitis, the following adverse reactions have been reported for PURIFIED WATER:
The following drugs have also been linked to oesophagitis in FDA adverse event reports:
OESOPHAGITIS has been reported as an adverse event in 3 FDA reports for PURIFIED WATER. This does not prove causation, but indicates an association observed in post-market surveillance data.
OESOPHAGITIS accounts for approximately 2.3% of all adverse event reports for PURIFIED WATER, making it a notable side effect.
If you experience oesophagitis while taking PURIFIED WATER, 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.