1,902 reports of this reaction
1.9% of all IPRATROPIUM BROMIDE reports
#8 most reported adverse reaction
NAUSEA is the #8 most commonly reported adverse reaction for IPRATROPIUM BROMIDE, manufactured by Boehringer Ingelheim Pharmaceuticals, Inc.. There are 1,902 FDA adverse event reports linking IPRATROPIUM BROMIDE to NAUSEA. This represents approximately 1.9% of all 98,863 adverse event reports for this drug.
Patients taking IPRATROPIUM BROMIDE who experience nausea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NAUSEA is a less commonly reported adverse event for IPRATROPIUM BROMIDE, but still significant enough to appear in the safety profile.
In addition to nausea, the following adverse reactions have been reported for IPRATROPIUM BROMIDE:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 1,902 FDA reports for IPRATROPIUM BROMIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 1.9% of all adverse event reports for IPRATROPIUM BROMIDE, making it a notable side effect.
If you experience nausea while taking IPRATROPIUM BROMIDE, 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.