66 reports of this reaction
1.8% of all IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE reports
#10 most reported adverse reaction
DIARRHOEA is the #10 most commonly reported adverse reaction for IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE, manufactured by American Health Packaging. There are 66 FDA adverse event reports linking IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE to DIARRHOEA. This represents approximately 1.8% of all 3,750 adverse event reports for this drug.
Patients taking IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE who experience diarrhoea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DIARRHOEA is a less commonly reported adverse event for IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE, but still significant enough to appear in the safety profile.
In addition to diarrhoea, the following adverse reactions have been reported for IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE:
The following drugs have also been linked to diarrhoea in FDA adverse event reports:
DIARRHOEA has been reported as an adverse event in 66 FDA reports for IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIARRHOEA accounts for approximately 1.8% of all adverse event reports for IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE, making it a notable side effect.
If you experience diarrhoea while taking IPRATROPIUM BROMIDE AND ALBUTEROL 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.