45 reports of this reaction
1.3% of all NITROUS OXIDE reports
#17 most reported adverse reaction
PULMONARY OEDEMA is the #17 most commonly reported adverse reaction for NITROUS OXIDE, manufactured by AGL Welding Supply Co., Inc.. There are 45 FDA adverse event reports linking NITROUS OXIDE to PULMONARY OEDEMA. This represents approximately 1.3% of all 3,365 adverse event reports for this drug.
NITROUS OXIDE has an overall safety score of 85 out of 100. Patients taking NITROUS OXIDE who experience pulmonary oedema should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
PULMONARY OEDEMA is a less commonly reported adverse event for NITROUS OXIDE, but still significant enough to appear in the safety profile.
In addition to pulmonary oedema, the following adverse reactions have been reported for NITROUS OXIDE:
The following drugs have also been linked to pulmonary oedema in FDA adverse event reports:
PULMONARY OEDEMA has been reported as an adverse event in 45 FDA reports for NITROUS OXIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
PULMONARY OEDEMA accounts for approximately 1.3% of all adverse event reports for NITROUS OXIDE, making it a notable side effect.
If you experience pulmonary oedema while taking NITROUS OXIDE, 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.